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Welcome to the

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Proteomics in Proximity podcast,
where your co-host

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Cindy Lawley and Sarantis Chlamydas
from Olink Proteomics

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talk about the intersection of proteomics
with genomics for drug target discovery,

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the application of proteomics
to reveal disease biomarkers,

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and current trends in using proteomics
to unlock biological mechanisms.

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Here we have your host,
Cindy and Sarantis.

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– Hello there.

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Welcome back to Proteomics in Proximity.

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I'm your host, Cindy Lawley,
with my co-host Sarantis Chlamydas.

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We have a very special episode for you
today.

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We have a few guests
coming to us from our new home,

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our new family, our new neighborhood,
Thermo Fisher Scientific.

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Some of you might recall that last summer
we completed

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the joining of Olink and Thermo
Fisher Scientific.

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I'm excited to report that we've got
Gianluca and, Karen to join us

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to talk about why and what that means
for all of us and all of you.

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Sarantis, do you want to tell us
a little bit more about our guests?

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– Thank you.

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I’m really pleased to welcome our guests
today.

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Truly honored to have Gianluca.

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And he's the Executive Vice
President of Thermo Fisher Scientific.

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Karen Nelson is Chief Scientific Officer.

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And, we are looking forward to discuss
about integration

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of all in proteomics
to the Thermo Fisher Scientific family

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and not only as a strategic alliance and,

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movement, but also the next step opening

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and promoting actually a world
that is healthier, that is safer

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and actually,
makes our life easier for everybody.

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I would like to pass the words to Gianluca
if you don't mind.

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I would like to know you
a little bit more better.

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And to I get to know your journey
and your career path that you had

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in Thermo Fisher and I am looking forward
to hearing from both of you.

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Thank you very much.

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– Sarantis, thank you very much.

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And, Cindy,
thanks for having both myself, and Karen,

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we were incredibly excited
to have the opportunity to join you.

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As you might remember, many months back,

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when we first talk, I knew about you.

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Not because of Olink but because
of this podcast that really helped me

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as a non-scientist over the years
to get acquainted

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with the magic world of proteomics.

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And having been 20 years in the industry,
I always thought

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that proteomics that the certain point
would be very transformative.

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And, indeed it is the case.

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And that's why ultimately we decided,
about a year ago to acquire Olink

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and now Olink being part of the Thermo
Fisher Scientific family.

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It is, truly being transformative
to the world of science.

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So I'm incredibly excited to be here.

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A little bit about me...

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– Can I just pop in and say that Gianluca
and I met at the castle in Uppsala

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at a dinner, and,

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And he knew about the podcast,
which was just so flattering to us.

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We were very excited to hear that. Sorry.

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Go ahead, Gianluca.

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– I knew about the pod.

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I was a fan. And, I'm continuing to be.

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– You even had it on your phone.

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You even showed me. I said, oh, please.

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He had it up.

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It was right at the end of the episode.

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I was gobsmacked.

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– I had the proof.

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The proof is in the pudding.

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You see, it wasn’t only marketing.

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– Frist step towards
trust between us, Gianluca.

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– Absolutely.

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Well, so.
And this was a little bit about me.

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I've been at Thermo Fisher Scientific
for the best part of the last 20 years.

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I was in Europe at first.

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Then I spent a few years in South America.

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In Brazil,
I moved, then in 2012, to China.

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Actually one of the biggest achievement
while I was in South America

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when I was running, what at that
time was Life Technologies in South

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America is meeting my wife,
and we together moved in China in 2012.

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When we moved in China,

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we announced that Thermo Fisher
was acquiring Life Technologies.

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We ended up spending five years
running, Thermo Fisher

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in China had two kids
that were born in Shanghai.

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So I think technically made in China
and then imported in the US

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when tariffs were not a thing
back in 2018,

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we moved to California
and then here in Boston,

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I now run our product
and technology businesses at the company

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and as said, I'm
incredibly excited about proteomics.

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We have ample time to talk about that,
over the course of this podcast.

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And so, without further ado,

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maybe I'll hand it over to Karen
to tell us a little bit about herself.

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– Absolutely. Looking forward.

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Looking forward.

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Actually, I would like to know,
I think as well

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that Karen has a tremendous career
and academic career.

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And it was she was leading
Craig Venter Institute, almost a decade.

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How was the transition from
I mean, it's a common question right,

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the transition from academy to a big
a technology industry institution?

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How did you find this?

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How was your vision? When do you change?

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– Well, Sarantis and Cindy,
thanks for having us today.

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It's such a pleasure to be 
with you guys,

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and Cindy, I'm just getting 
caught up on your podcast,

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but they really are great.

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So thanks for doing that.

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– Aw thanks.

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– You know, so I joined four years ago
and, Sarantis, to your question,

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probably one of the best career moves of
my probably is well,

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I'm by now, I'm sure it has been the best
career decision of my life.

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I spent close to 23 years

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in a non-for-profit research world

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with the Venter team, and they're,
you know, they were part of the team

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that did the human genome,

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my biggest claim to fame was doing
the first human microbiome.

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So a lot of time spent in genomics
technologies and then my coming over

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to Thermo Fisher and seeing the breadth
and possibilities of what we have

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all the way from instruments
through consumables in the life sciences

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through clinical trials
that has been such an amazing,

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experience for me, both in terms of people

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and learning and the willingness
of everybody wanting to partner.

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And then,

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you know, when I heard that you guys
were joining the family, it was like,

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you know, Gainluca, and I were like,
yes, this is perfect

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because it was such a nice complement
to what we had already in-house

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and had the potential to really accelerate
what we're doing to make the world

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healthier and safer.

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So thanks for having us here
today.

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– Yeah, thanks, Karen.
Because we do. We feel very welcome.

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– Wonderful.

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– I just want to highlight
and put on records that you said

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that was the best
move of your life and career.

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– She moved from Craig Venter to me.

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And so I don't know
if I have the same scientific pedigree,

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I have to say, but I think that there's
a compliment coming.

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– Well, it's
been such a pleasure to be here.

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– He’s throwing down 
the gantlet, Karen, to Craig.

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– I know, I know.

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– Now I'm thinking
maybe we'll hear from Craig.

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– But, you know.

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But just the magnitude
and the impact of Thermo Fisher.

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You know, I am one of those,

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who grew up on Thermo Fisher
reagents and instruments and supplies.

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You know, it was Gibco
in every aspect of your lab,

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for example, and different pieces
of equipment and thermal cyclers.

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So it's actually,
you know, my opportunity to be back,

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at home, just like you guys are here now.

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– And I'll say it's not an easy thing
to make a transition that that layers

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on what Craig Venter accomplished
and what you accomplished with him.

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I mean, just
the whole history is just phenomenal.

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– Well Cindy, you're part of that too.

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You made the jump.
So you know what it's like.

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– Yeah.

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So that's why I'm

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complimenting us both
for having such a good...

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– Good mentors and great guidance.

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– That's right.

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It's all about having a cool technology,
having wonderful people around

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you and those wonderful people
then create a good culture.

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And I think with that in place,
changing the world, feeling

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like we've got a purpose, I mean, that's
just icing on the cake, right?

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So, Gianluca, we've got mass spectrometry,

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an amazing capability
here at Thermo Fisher.

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And I will say, I as Karen says,
I come from the genetics world.

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So, so proteins
have always been really scary to me.

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I felt like Olink gives me a little bit
of a,

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an easing into proteomics.

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But why Olink in the context

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of the enormous capabilities
at Thermo Fisher

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using mass spectrometry and the advances
that we're seeing in that space?

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– Yes.

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Obviously starts from the

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understanding
of the importance of proteins

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and the importance of proteins,
to obviously our,

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incredibly complex
and fascinating biological systems.

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And as a leader in proteomics,
through our mass spectrometry franchise,

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we had the opportunity
to have great insights

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on what was happening in the market
and also the understanding that,

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not only having solutions
that are helping you to go incredibly deep

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and, in a way, in an untargeted fashion

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to study
proteins was not enough to be able

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to provide to our customers
the full breadth of what they truly need,

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which to us is also a high affinity
method.

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A throughput like, Olink provides

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that truly is being transformational.

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When you look at the result of the UK
Biobank

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in terms of both
the amount of information that,

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the UK

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Biobank cohort has been able to create
and the one that is ahead of us,

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but more importantly,
the number of publications

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and the understanding of correlation
between the presence of protein,

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their level disease,
this has been truly transformational.

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And the pivotal moment thinking science.

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And we'll discover more and more.

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And so, we felt that was very natural

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to actually combine,
the all the technology

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with the incredible leadership
that we already had in mass spectrometry.

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And indeed, we are now seeing how engaging
with customers,

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the two technology
can be incredibly complementary

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to have a more comprehensive
understanding of the human proteome.

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And I can't wait to see
what's going to happen

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in the next few years,
because I do believe

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there's going to be transformational
in the way that ultimately

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we actually prevent
then detect and treat diseases

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that today are not, treated
as well as they should.

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– To monitor, right? Who's really at risk?

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And I, I joke about the Goldilocks,

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too hot to cold and just right.

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And I don't want to dismiss
your microbiome

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metabolites,
but they are so hot, they move so quickly.

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Right?
DNA moves at the pace of generations.

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That's really slow.

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It's hard to nudge, but proteins,

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it's just, it's the baby bear bowl.

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It's just fabulous.

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– So, Cindy,

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I wanted to pick up on something
you said about proteomics being scary.

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I don't know if it was scary
as much as we didn't have the right tools.

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Right.

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And now, finally, we do have to. And,

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if you think about Astral and Astral Zoom
and how deep you can go on a sample now,

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I mean, it's unbelievable
what's changed over

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the past 15, 20 years
in terms of technology development.

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So we're now in a better comfort, space.

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And to Gianluca’s point about integrating
the Olink data with, proteomics data.

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I mean, it's such a tremendous advance
for science.

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And from where I sit, yeah, for sure.

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– And I guess I think of it more as scary
from a geneticist point of view,

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where we had this,
you know, certainly in 2007

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when we advanced to the
to the massively parallel sequencing

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and being able to analyze those data,
right, that we just shifted the burden

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from the collection of the data
to the reconstituting the data

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and comparing it to reference genomes

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and handling
those data or even transcriptomic data

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just feels a little more,
you know, it's A C T  and G

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right there isn't the conformational
or the, conformational complexity

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or the protein protein
interaction complexity, but I think,

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geneticists are really getting comfortable
with full length proteins.

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And then mass Spec is going to be
the only way, today to dig

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into proteome forms, to dig into
what are the post-translational

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modified aspects of those proteins
that are actually,

237
00:13:22,708 --> 00:13:24,291
providing the bulk of those signals?

238
00:13:24,291 --> 00:13:26,875
And, of course, we're seeing from the UK
Biobank data

239
00:13:26,875 --> 00:13:31,208
amazing signatures of 5 to 20 proteins
that are predicting disease

240
00:13:31,458 --> 00:13:33,583
better than anything
a doctor has available today.

241
00:13:33,583 --> 00:13:36,250
Like this is, you know, just echoing
on what you're saying.

242
00:13:36,250 --> 00:13:38,666
Gian, it's a very exciting time now.

243
00:13:38,666 --> 00:13:43,291
– I mean, I want to follow up
in on Gianluca’s comment about UK Biobank.

244
00:13:43,291 --> 00:13:46,583
We see recently also that pharma
investing from these data sets,

245
00:13:46,583 --> 00:13:49,833
right, of generating real world
evidence, real world data.

246
00:13:50,333 --> 00:13:53,916
And we see that they invest in cultural
on platforms like Olink.

247
00:13:54,416 --> 00:13:58,291
How will you see both of you
the role that can play in this platform

248
00:13:58,291 --> 00:14:03,375
kind of way of working pharma
together with governmental institutions,

249
00:14:03,625 --> 00:14:06,875
with academic institutions
to enable precision medicine?

250
00:14:07,166 --> 00:14:11,125
How do you see Thermo Fisher plays a role
that are and having all of this

251
00:14:11,583 --> 00:14:14,875
weight and breadth of
multi-omics approache?

252
00:14:15,458 --> 00:14:16,625
– It’s a great question.

253
00:14:16,625 --> 00:14:20,541
And, you know, maybe because, the probably

254
00:14:20,541 --> 00:14:24,208
only non-scientist
of the crew here in the pod,

255
00:14:24,208 --> 00:14:28,166
– I disagree.
– You disagree?

256
00:14:28,166 --> 00:14:29,458
– Honorary member.
– No, you’re scientist.

257
00:14:29,458 --> 00:14:30,875
– Honorary member.

258
00:14:30,875 --> 00:14:33,666
– You are absolutely a scientist.

259
00:14:33,666 --> 00:14:37,916
– I learned in street fighting,
spending a lot of time with customers.

260
00:14:37,916 --> 00:14:43,416
But, you know, I've been thinking a lot
and being, at heart,

261
00:14:44,250 --> 00:14:47,250
a lover of technology and innovation.

262
00:14:48,000 --> 00:14:50,250
I've been, obviously

263
00:14:50,250 --> 00:14:53,250
very impressed
what is happening in the world of,

264
00:14:53,625 --> 00:14:56,791
automotive technologies
and, transportation?

265
00:14:57,541 --> 00:14:59,625
We now have self-driving cars.

266
00:14:59,625 --> 00:15:03,750
I wake up in the morning and my Tesla

267
00:15:04,208 --> 00:15:07,833
doesn't even need me
to tell where I'm going,

268
00:15:07,833 --> 00:15:12,125
because the Tesla knows that
more probably I’m going to the office.

269
00:15:12,208 --> 00:15:15,208
So I sit on my Tesla and there's already,

270
00:15:15,333 --> 00:15:18,333
a predefined destination in the morning.

271
00:15:19,291 --> 00:15:21,541
And then I put self driving

272
00:15:21,541 --> 00:15:24,541
and the car drives itself to the office.

273
00:15:24,708 --> 00:15:26,458
Intervention is very limited.

274
00:15:27,500 --> 00:15:29,375
And my hope is that

275
00:15:29,375 --> 00:15:33,208
at a certain point,
health becomes the same.

276
00:15:34,291 --> 00:15:37,291
We are on autopilot.

277
00:15:37,500 --> 00:15:40,500
And to be able to do that
you actually need,

278
00:15:41,500 --> 00:15:44,916
devices and detectors and signals.

279
00:15:45,291 --> 00:15:49,083
And I think proteins are providing
just that.

280
00:15:50,000 --> 00:15:54,416
We actually don't understand everything
to the same extent

281
00:15:54,416 --> 00:15:58,833
that, digital technologies
are able to understand,

282
00:15:59,458 --> 00:16:04,291
visual signs
and help a car driving itself yet.

283
00:16:04,875 --> 00:16:09,291
But I think that's going to be obviously,
a big transformation.

284
00:16:09,833 --> 00:16:13,125
And that is why I think to your question,
pharma

285
00:16:13,125 --> 00:16:18,666
companies are so interested
now in getting a head start in proteomics.

286
00:16:19,250 --> 00:16:21,750
Because, we've seen again,

287
00:16:21,750 --> 00:16:26,791
through some of the result of the UK
Biobank protein

288
00:16:27,208 --> 00:16:32,916
signatures and this, poly protein,
you can call it race course.

289
00:16:32,916 --> 00:16:37,250
My opinion, but I'll leave it
to the scientists on the part to confirm

290
00:16:37,500 --> 00:16:41,666
is more than rescore,
I think very different to look at poly

291
00:16:41,666 --> 00:16:46,291
protein signatures and polygenic
risk scores as an example.

292
00:16:46,625 --> 00:16:50,708
That's why I think pharma so interested
in this poly protein signature

293
00:16:51,041 --> 00:16:55,083
as an indicator
of either an early onset of disease

294
00:16:55,500 --> 00:16:59,583
or perhaps an indication of,
response to therapy.

295
00:17:00,458 --> 00:17:03,500
So again, over time, I think the,

296
00:17:04,000 --> 00:17:06,833
utility of protein

297
00:17:06,833 --> 00:17:10,666
signature
is going to be quite broad in nature,

298
00:17:10,666 --> 00:17:16,125
whether he's prevention, early detection,
whether he's response to treatment.

299
00:17:17,333 --> 00:17:18,458
And I

300
00:17:18,458 --> 00:17:22,416
think more things that can be done
through, those signatures.

301
00:17:22,416 --> 00:17:24,666
So it's quite exciting.

302
00:17:24,666 --> 00:17:27,666
Does the interest in the space,

303
00:17:28,041 --> 00:17:30,333
the key to me is still

304
00:17:30,333 --> 00:17:34,416
generating millions and millions
of data points so that ultimately

305
00:17:34,416 --> 00:17:38,958
we can apply artificial intelligence
and truly get to it to cells.

306
00:17:38,958 --> 00:17:43,208
Do I can I call self-driving human
or is a bit to, provocative?

307
00:17:43,208 --> 00:17:44,208
I don't know.

308
00:17:44,208 --> 00:17:46,625
– I think self,

309
00:17:46,625 --> 00:17:48,000
so why do we want to call that?

310
00:17:48,000 --> 00:17:49,166
I mean, it's a really good question.

311
00:17:49,166 --> 00:17:50,708
We should come up with a phrase, Gian,

312
00:17:50,708 --> 00:17:54,833
I don't know that self-driving human,
but it’s self, I mean, we're certainly

313
00:17:54,833 --> 00:17:57,916
putting power in the hands
of the individual, right? Yes.

314
00:17:57,916 --> 00:18:02,083
We the community, the scientific community
by building such tools.

315
00:18:02,333 --> 00:18:05,833
And I think this point about self-driving,
I love the comparison.

316
00:18:05,833 --> 00:18:09,791
You know, I love a good analogy, but,
you know, I was talking to one of the

317
00:18:09,791 --> 00:18:13,666
I live in the Bay area, this, you know,
you can't swing a dead cat without hitting

318
00:18:13,666 --> 00:18:18,708
somebody who's been involved
in some aspect of collecting self-driving.

319
00:18:18,708 --> 00:18:20,000
I would never swing a cat, by the way.

320
00:18:20,000 --> 00:18:25,458
Is involved in some aspect
of this technological advance.

321
00:18:25,458 --> 00:18:29,833
And even where I used to live
in the agricultural belt of California,

322
00:18:30,250 --> 00:18:33,750
they used an old air force base
to do some of the practicing out of that.

323
00:18:33,750 --> 00:18:38,041
But but what turned out to be
the most important thing is that the right

324
00:18:38,041 --> 00:18:42,375
data were used
the minute you have incorrect data.

325
00:18:42,666 --> 00:18:45,125
And here I'm calling back to specificity.

326
00:18:45,125 --> 00:18:45,416
Right.

327
00:18:45,416 --> 00:18:48,416
And the importance of knowing exactly
what protein you're measuring.

328
00:18:48,583 --> 00:18:51,166
If the minute you have wrong data,
the algorithm

329
00:18:51,166 --> 00:18:52,833
can't discern the difference.

330
00:18:52,833 --> 00:18:56,916
And so I think that was the turning point
based upon the conversations

331
00:18:56,916 --> 00:19:03,000
I've had with a few of these folks of,
of being able to, to really make that work

332
00:19:03,000 --> 00:19:06,333
because it's phenomenal
to see those cars drive themselves.

333
00:19:06,333 --> 00:19:10,541
They can come pick you up at the curb
with not a driver in the seat.

334
00:19:10,583 --> 00:19:12,125
It's impressive.

335
00:19:12,125 --> 00:19:12,500
– Actually.

336
00:19:12,500 --> 00:19:16,000
You're not far away from the concept of
digital twins, right in pharma convention

337
00:19:16,333 --> 00:19:21,500
that they have the digital twins
where actually can project things in AI.

338
00:19:21,500 --> 00:19:21,958
Right.

339
00:19:21,958 --> 00:19:25,916
And predict things in AI, I think that's
we are really close on this,

340
00:19:25,916 --> 00:19:27,833
really close on this on this era.

341
00:19:27,833 --> 00:19:29,625
– And the virtual cell. Right.

342
00:19:29,625 --> 00:19:30,416
We could navigate through it.

343
00:19:30,416 --> 00:19:33,958
– So Cindy, just pick up on what
one of the points Gianluca was making

344
00:19:33,958 --> 00:19:34,541
is that,

345
00:19:34,541 --> 00:19:37,083
you know, some of the preliminary data
coming out of UK

346
00:19:37,083 --> 00:19:40,416
Biobank in terms of stratifying
patients is really amazing.

347
00:19:40,458 --> 00:19:40,916
Right.

348
00:19:40,916 --> 00:19:46,583
And so to Gianluca's, point be,
you know, the early diagnosis,

349
00:19:46,625 --> 00:19:51,541
like the protein signature that's coming
really early on, we're going to be

350
00:19:51,541 --> 00:19:56,791
at a point where we can use that to change
the trajectory of health or treatment.

351
00:19:56,791 --> 00:19:59,916
And I think we're just at the beginning
here.

352
00:19:59,916 --> 00:20:04,875
And, you know, you know, I just think
it's going to change how we think

353
00:20:04,875 --> 00:20:08,583
about human health could go all the way
to animal health, environmental health.

354
00:20:08,583 --> 00:20:11,916
But it's just such an amazing opportunity
for the field.

355
00:20:11,916 --> 00:20:13,166
When you start to look at

356
00:20:13,166 --> 00:20:16,041
the initial implications of the data
that's coming out.

357
00:20:16,041 --> 00:20:20,166
And I, I think, Gianluca, we have multiple
collaborations now, right?

358
00:20:20,166 --> 00:20:21,583
It's not just the UK Biobank.

359
00:20:21,583 --> 00:20:24,000
I think it's we're processing...

360
00:20:24,000 --> 00:20:27,000
– Topmed, FinnGen, yeah. – Yeah.

361
00:20:27,208 --> 00:20:29,958
– We're involved in our future health
where, yeah, there's

362
00:20:29,958 --> 00:20:33,750
there's so many places
where there's opportunities.

363
00:20:33,750 --> 00:20:37,458
And I think it just for context on UK
Biobank, what a sweet data

364
00:20:37,500 --> 00:20:41,250
set that is just to remind listeners
that, you know,

365
00:20:41,250 --> 00:20:45,125
those collections were made
for individuals between 40 and 67 years

366
00:20:45,125 --> 00:20:49,375
of age, and it's been almost 20 years
for them to develop diseases.

367
00:20:49,375 --> 00:20:52,375
And so to Karen's
point to Gian, to your point,

368
00:20:52,375 --> 00:20:56,666
this is a beautiful set to be able
to look at those baseline blood samples

369
00:20:56,916 --> 00:21:01,291
and see the signatures for the same
diseases in different individuals.

370
00:21:01,625 --> 00:21:05,250
And that has, you know, certainly
coming out of, Ruth Travis's group,

371
00:21:06,125 --> 00:21:09,583
they've been able to do that in cancer
that hit the UK news last year around

372
00:21:09,583 --> 00:21:14,250
how they could see a median of 12 years
before diagnosis of cancer.

373
00:21:14,250 --> 00:21:16,291
12 years. That's phenomenal. Right?

374
00:21:16,291 --> 00:21:19,083
A minimum of seven years.
That was what hit the news.

375
00:21:19,083 --> 00:21:21,958
And then, and then of course,
the Carrasco Zanini paper

376
00:21:21,958 --> 00:21:25,958
coming out of Claudia Langenberg's lab,
where 67 out of the 200 diseases

377
00:21:26,208 --> 00:21:29,958
in just the pilot of the 
UK Biobank Pharma Proteomics Project.

378
00:21:30,791 --> 00:21:33,166
They were able to see these 5 to 20

379
00:21:33,166 --> 00:21:36,416
protein signatures that outperform
anything a doctor has available today.

380
00:21:36,416 --> 00:21:40,250
So just for some context, that
some of that exciting stuff coming out of

381
00:21:41,791 --> 00:21:44,583
that study, that pilot and those pilot

382
00:21:44,583 --> 00:21:48,458
data are available
for application to use them,

383
00:21:48,458 --> 00:21:51,958
and they're free for many, many,
many academic institutions

384
00:21:51,958 --> 00:21:55,083
So it's, it's an exciting time.

385
00:21:55,666 --> 00:21:58,666
– One of the thing I want to add,
one thing that is,

386
00:21:58,791 --> 00:22:01,708
maybe the elephant in the room
or the human in the room,

387
00:22:01,708 --> 00:22:03,541
call it, the way we want.

388
00:22:03,541 --> 00:22:04,791
– The self-driving human.

389
00:22:05,000 --> 00:22:06,625
– The self-driving human.

390
00:22:06,625 --> 00:22:09,583
But, in serious terms.

391
00:22:09,583 --> 00:22:12,375
One of the things that I’ve been,

392
00:22:12,375 --> 00:22:16,291
fascinated with
is ultimately human psychology.

393
00:22:16,291 --> 00:22:21,041
And I think I'm not misquoting this, but,

394
00:22:21,333 --> 00:22:24,333
in a study that was run a few years back,

395
00:22:24,958 --> 00:22:28,625
they highlighted
how 50% of the individuals

396
00:22:28,625 --> 00:22:33,041
that should take medicines
that are critical due

397
00:22:33,041 --> 00:22:36,916
to the chronic condition
and in many cases, a life

398
00:22:36,916 --> 00:22:40,833
saving, medicines,
they're in noncompliance.

399
00:22:40,833 --> 00:22:45,166
50% of them die in noncompliance,
which tells you,

400
00:22:45,791 --> 00:22:50,625
the fact that, for some reason,
humans are not very,

401
00:22:51,125 --> 00:22:53,791
self caring, if you wish.

402
00:22:53,791 --> 00:22:56,000
And so one thing that

403
00:22:56,000 --> 00:23:00,958
I think is going to be very important
to your point on the amount of available

404
00:23:00,958 --> 00:23:05,541
information, is
how do we disseminate this information?

405
00:23:05,833 --> 00:23:09,000
How do we make sure there's
enough, learning,

406
00:23:09,666 --> 00:23:13,666
opportunities both for doctors
but also for individuals

407
00:23:14,041 --> 00:23:16,791
to become more self-aware

408
00:23:16,791 --> 00:23:20,416
on how they actually can stop the car
before the car crashes.

409
00:23:20,708 --> 00:23:23,458
With the analogy of self-driving cars, a

410
00:23:23,458 --> 00:23:26,458
self-driving car normally doesn't crash.

411
00:23:27,000 --> 00:23:30,833
And I think from a health standpoint,
we should make sure

412
00:23:30,833 --> 00:23:35,500
that we prevent disease more effectively
going forward.

413
00:23:35,875 --> 00:23:39,125
With all of this insight and information
that we have available.

414
00:23:39,416 --> 00:23:42,458
Then one of the concerns I have,
I don't know your perspective, is

415
00:23:42,625 --> 00:23:47,500
how do we influence culture
and who is going to be, actually

416
00:23:47,500 --> 00:23:51,791
helping consumers to do a better job

417
00:23:51,791 --> 00:23:54,791
in taking good care of themselves?

418
00:23:54,791 --> 00:23:57,458
That, to me, is still an unresolved issue.

419
00:23:57,458 --> 00:24:00,625
If we don't resolve it as a society, then

420
00:24:00,625 --> 00:24:04,750
it would be very difficult
to take full advantage of, these tools.

421
00:24:04,750 --> 00:24:07,750
But maybe these alternative solutions,

422
00:24:07,916 --> 00:24:12,291
that will, be implemented
over time as a result of,

423
00:24:12,833 --> 00:24:16,916
now much better tools to help,
consumers and patients.

424
00:24:17,750 --> 00:24:21,000
– Karen, do you have ideas about that
from the genetics space?

425
00:24:21,000 --> 00:24:21,250
Right.

426
00:24:21,250 --> 00:24:24,250
This feels like a parallel,

427
00:24:24,333 --> 00:24:26,875
of education needed, right.

428
00:24:26,875 --> 00:24:31,958
That what what was what was what helped
us there from your perspective?

429
00:24:33,375 --> 00:24:33,583
– Well there’s

430
00:24:33,583 --> 00:24:37,416
I mean, to Gianluca's point it
probably it has to happen in parallel,

431
00:24:37,416 --> 00:24:42,125
right, to get absorption
into the general population.

432
00:24:42,125 --> 00:24:45,875
I think back then we had set aside
funds for like ethical,

433
00:24:45,875 --> 00:24:47,833
legal and social implications.

434
00:24:47,833 --> 00:24:50,125
Remember all of that good stuff,
Cindy? 

435
00:24:50,125 --> 00:24:50,458
– Yeah. Oh Yeah.

436
00:24:50,458 --> 00:24:54,750
– And, it was a percentage of all funding
going into genomic research was,

437
00:24:55,583 --> 00:24:58,958
used for like education and legal work
and getting,

438
00:25:00,291 --> 00:25:02,541
because there were a lot of questions.

439
00:25:02,541 --> 00:25:03,625
A lot of concerns.

440
00:25:03,625 --> 00:25:06,000
And not everybody is trained in science.

441
00:25:06,000 --> 00:25:07,416
And so they don't understand.

442
00:25:07,416 --> 00:25:11,666
And, you know,
we tend to be positive and can only,

443
00:25:12,833 --> 00:25:15,208
just try to discuss
the positive implications.

444
00:25:15,208 --> 00:25:16,083
But there are concerns

445
00:25:16,083 --> 00:25:19,583
about some of these, research areas
that people don't quite understand.

446
00:25:19,958 --> 00:25:25,458
And I think, the education and the value
and highlighting, you know, like the car

447
00:25:26,708 --> 00:25:27,750
analogy.

448
00:25:27,750 --> 00:25:30,541
Gianluca, you're saying
that when the light comes on, on the car,

449
00:25:30,541 --> 00:25:34,166
take it in and don't wait till like,
the engine shuts down right.

450
00:25:34,166 --> 00:25:36,416
And we're getting to the point
where we can

451
00:25:36,416 --> 00:25:39,416
have that light come on really early
when there's a problem in the car.

452
00:25:40,291 --> 00:25:41,875
Not on an Italian car though, right?

453
00:25:41,875 --> 00:25:44,875
I'm talking about
in other parts of the world. So.

454
00:25:44,875 --> 00:25:48,875
But I think, as a society, Cindy,
we probably need to start

455
00:25:48,875 --> 00:25:51,333
having those conversations
about getting the information out,

456
00:25:51,333 --> 00:25:52,833
getting the positive findings out.

457
00:25:52,833 --> 00:25:56,500
You know, it's right now, it's
so positive, like, how do we get that out

458
00:25:57,000 --> 00:26:00,958
in words
that the general community can understand?

459
00:26:00,958 --> 00:26:03,708
And I think it's up to us
to try and accelerate that.

460
00:26:03,708 --> 00:26:06,708
– And isn't it easier
because proteins aren't

461
00:26:06,875 --> 00:26:09,625
tied to our personal genetic information,
right.

462
00:26:09,625 --> 00:26:10,541
– Right, it should be.

463
00:26:10,541 --> 00:26:15,250
– That might be because, yeah, it's
not an identifier of us as individuals.

464
00:26:15,250 --> 00:26:17,208
Our protein signature.

465
00:26:17,208 --> 00:26:18,958
– Right. But it's hard to understand, right.

466
00:26:18,958 --> 00:26:22,958
Because you talk about proteins
and proteoforms and splicing

467
00:26:22,958 --> 00:26:24,083
and all this good stuff.

468
00:26:24,083 --> 00:26:29,875
And so it's about how to translate
that in words that, the average person

469
00:26:30,250 --> 00:26:34,500
can understand the benefit of the research
that's ongoing right now.

470
00:26:35,333 --> 00:26:37,541
– I think to your point,
I mean, it's also really important

471
00:26:37,541 --> 00:26:38,916
not only to generate the data, right,

472
00:26:38,916 --> 00:26:43,125
but having the tools to interpret
the data and make sense out of this data.

473
00:26:43,125 --> 00:26:44,458
And I think that's also really important.

474
00:26:44,458 --> 00:26:47,500
We'll come to the future and it'll come
really important to the future as well.

475
00:26:47,666 --> 00:26:51,291
Interpret the data, make them easy
for the people to understand

476
00:26:51,291 --> 00:26:53,750
and make the right use on that. Yeah,
that's an excellent point, Karen.

477
00:26:53,750 --> 00:26:57,291
I actually would like to follow up
on this, Karen, if you have this NGS

478
00:26:57,333 --> 00:27:02,250
background and experience, what excites
you more in this NGS proteomics nowadays?

479
00:27:02,250 --> 00:27:05,666
And do you see this like a game changer
for clinical trials for example?

480
00:27:05,666 --> 00:27:09,208
Do you see that will make clinical trials
smarter having NGS

481
00:27:09,208 --> 00:27:12,458
proteomics integrated
to the omics pipelines, for example.

482
00:27:12,625 --> 00:27:13,958
– Quick answer is yes.

483
00:27:13,958 --> 00:27:15,750
You know, you think about NGS.

484
00:27:15,750 --> 00:27:17,375
It's like a static point

485
00:27:17,375 --> 00:27:20,416
in time that you're understanding
what's going on in the cell.

486
00:27:20,416 --> 00:27:21,416
Now, we can actually

487
00:27:22,458 --> 00:27:24,333
understand over a time period

488
00:27:24,333 --> 00:27:27,833
how a cell is behaving, how it's reacting,
what it what it's doing.

489
00:27:28,083 --> 00:27:30,416
You can do it with a human.
You can do it with a bacterial cell.

490
00:27:30,416 --> 00:27:31,458
You can do it with a plant.

491
00:27:31,458 --> 00:27:33,958
I mean, you can understand

492
00:27:33,958 --> 00:27:38,666
what the DNA has resulted
in terms of activity at the cell level.

493
00:27:38,666 --> 00:27:40,250
And I think it's so exciting.

494
00:27:40,250 --> 00:27:41,666
I mean, genomics was exciting.

495
00:27:41,666 --> 00:27:47,250
We built massive informatics resources,
software resources, massive tools, AI.

496
00:27:47,250 --> 00:27:50,250
We were using all these tools back then,

497
00:27:50,291 --> 00:27:53,291
but now we have a chance
to actually understand

498
00:27:54,000 --> 00:27:57,500
what are the messages coming out
and what are they turning into.

499
00:27:57,500 --> 00:28:01,708
And how can not that we want to stop it,
but how can we use that information

500
00:28:01,833 --> 00:28:05,916
to influence the outcomes
and our health in the long term?

501
00:28:05,916 --> 00:28:10,458
And I think it's gonna,
over time, become a critical part of,

502
00:28:11,583 --> 00:28:13,916
you know,
a companion, part of clinical trials?

503
00:28:13,916 --> 00:28:14,583
I would think so.

504
00:28:14,583 --> 00:28:18,125
I don't do that on a daily basis,
but I would absolutely believe that

505
00:28:18,625 --> 00:28:21,875
they're going to you can take a plasma
sample on a daily basis

506
00:28:21,875 --> 00:28:25,916
and look at how certain
protein markers are fluctuating.

507
00:28:25,916 --> 00:28:27,833
Imagine a time like that. Right.

508
00:28:27,833 --> 00:28:31,500
– Well, Chris Whelan talked about this
in depression where they had

509
00:28:31,500 --> 00:28:34,375
three endotypes based on proteins
after the clinical trial.

510
00:28:34,375 --> 00:28:36,375
Right. So this is an in that trial.

511
00:28:36,375 --> 00:28:39,208
But they responded differently
to the therapy.

512
00:28:39,208 --> 00:28:40,125
Each of those three.

513
00:28:40,125 --> 00:28:40,625
Yeah sorry.

514
00:28:40,625 --> 00:28:41,291
Go ahead Karen.

515
00:28:41,291 --> 00:28:44,625
– No I was just saying that
I think you guys had a partnership where

516
00:28:44,625 --> 00:28:50,166
initial outputs from Olink data turned
actually into, diagnostic in the clinic.

517
00:28:50,166 --> 00:28:50,625
Right.

518
00:28:50,625 --> 00:28:54,875
And it took a couple of years,
but I believe that that's going

519
00:28:54,875 --> 00:28:59,125
to become at scale
that we can have these early biomarkers

520
00:28:59,583 --> 00:29:02,791
being detected as a result of
the technologies that we're,

521
00:29:03,958 --> 00:29:05,750
fostering in-house.

522
00:29:05,750 --> 00:29:06,541
I really believe that.

523
00:29:06,541 --> 00:29:09,625
– Yeah, yeah, those diseases
and there's application

524
00:29:09,625 --> 00:29:13,416
and disease specific signatures
that our customers are building.

525
00:29:13,416 --> 00:29:18,250
I think that is one of the most exciting
things I was excited about in joining

526
00:29:18,250 --> 00:29:22,291
the Thermo Fisher family is that we can
we can accelerate those.

527
00:29:22,958 --> 00:29:23,958
Right.

528
00:29:23,958 --> 00:29:26,958
– And Sarantis, my last happy,
happy point.

529
00:29:27,000 --> 00:29:30,000
Imagine being able to live
through the genomics revolution

530
00:29:30,416 --> 00:29:32,750
and landing where I can live
through the proteomics revolution.

531
00:29:32,750 --> 00:29:35,208
– That’s amazing. 
– I mean,

532
00:29:35,208 --> 00:29:38,208
not a lot of people
get that opportunity, right, Cindy?

533
00:29:38,375 --> 00:29:39,583
– That's right, that's right.

534
00:29:39,583 --> 00:29:43,500
It's pretty special, it really is.

535
00:29:43,666 --> 00:29:46,916
– What do you think also
this will open the door to let's say FDA

536
00:29:46,916 --> 00:29:50,416
and to other and let's say institutions
that can be biomarkers

537
00:29:50,416 --> 00:29:54,166
that are approved will make probably
all of these procedures much easier.

538
00:29:54,208 --> 00:29:55,916
Having all of these nice data sets.

539
00:29:55,916 --> 00:29:58,708
What is your opinion
there, Gianluca, on that?

540
00:29:58,708 --> 00:30:01,958
– I think regulators, have their hands full,

541
00:30:02,375 --> 00:30:06,125
to stay up to speed
with the technology for sure.

542
00:30:06,125 --> 00:30:07,708
And it's actually,

543
00:30:08,750 --> 00:30:11,000
refreshing to see that

544
00:30:11,000 --> 00:30:14,125
I think we had recently one of the first,

545
00:30:15,208 --> 00:30:17,708
AI driven biomarkers

546
00:30:17,708 --> 00:30:21,041
approved, in the pathology space.

547
00:30:21,291 --> 00:30:23,041
If I'm not mistaken.

548
00:30:23,041 --> 00:30:27,625
And so it tells you that,
they're starting to move at pace.

549
00:30:28,083 --> 00:30:31,083
And that's a very good news.

550
00:30:31,291 --> 00:30:33,625
By the way, I Chatgpted

551
00:30:33,625 --> 00:30:37,875
the data point
that I quoted on Nonadherence,

552
00:30:38,458 --> 00:30:41,750
and, in fact,
there was a study from the W.H.O.

553
00:30:41,750 --> 00:30:46,708
that says that, Nonadherence can account
for up to 50% of treatment failure.

554
00:30:47,125 --> 00:30:50,250
And just to put this in context,
in the US,

555
00:30:50,250 --> 00:30:53,250
around 125,000 deaths

556
00:30:53,291 --> 00:30:56,916
and out to 25% hospitalization each year,

557
00:30:57,750 --> 00:31:01,708
that are driven from nonadherence,
with medication.

558
00:31:01,708 --> 00:31:06,208
So, it's indeed highlighting
how the need of,

559
00:31:07,291 --> 00:31:10,375
you know, information and education

560
00:31:10,375 --> 00:31:13,375
of the patient population
is, super critical.

561
00:31:13,708 --> 00:31:16,166
But also,
I think technology plays a big role.

562
00:31:16,166 --> 00:31:17,250
Why we're seeing...

563
00:31:17,250 --> 00:31:19,958
– Sentry Mode, right, Gianluca?
I mean.

564
00:31:20,083 --> 00:31:21,666
– Sentry Mode. Yes.

565
00:31:21,666 --> 00:31:23,791
– Get a pop up.

566
00:31:23,791 --> 00:31:28,708
– Get a pop up, but, you know, in that
case, you obviously have the car that,

567
00:31:29,666 --> 00:31:34,041
allows you to do that in a patient ward.

568
00:31:34,083 --> 00:31:38,333
Actually, you need technology to be able
to detect, as Karen was highlighting.

569
00:31:39,083 --> 00:31:42,416
What about detecting this biomarker
on a continuous basis?

570
00:31:42,750 --> 00:31:46,541
And I feel we're still
in the era of mainframe,

571
00:31:47,375 --> 00:31:50,125
in the life science space.

572
00:31:50,125 --> 00:31:52,375
You have this big instrument...

573
00:31:52,375 --> 00:31:55,375
– Or it’s the Volkswagen Bub from 1966.

574
00:31:55,708 --> 00:31:57,333
– Yes.

575
00:31:57,333 --> 00:31:59,250
That's a good analogy.

576
00:31:59,250 --> 00:32:02,250
– Beautiful car, but. 
– We use Fiat.

577
00:32:02,916 --> 00:32:07,208
You know,
I know that you now you're in the US.

578
00:32:07,208 --> 00:32:10,208
So you say Fiat means fix it again, Tony.

579
00:32:10,541 --> 00:32:11,916
But I

580
00:32:11,916 --> 00:32:14,875
as an Italian,
I could take offense for that.

581
00:32:14,875 --> 00:32:16,625
But actually...

582
00:32:16,625 --> 00:32:17,958
– Yeah, you’ll get in trouble.

583
00:32:17,958 --> 00:32:24,291
– It was my first car and 
I truly enjoyed my Fiat.

584
00:32:24,291 --> 00:32:27,375
But I think technology
will need to play a big role.

585
00:32:27,375 --> 00:32:30,375
And I could envision over time

586
00:32:30,541 --> 00:32:35,458
we already have much smaller
and compact sequencers

587
00:32:35,458 --> 00:32:40,166
and the we know the detection technology
for Olink case sequencing.

588
00:32:40,166 --> 00:32:44,375
But over time, we're going to have smaller
and smaller technologies

589
00:32:44,375 --> 00:32:48,166
that can be ultimately integrated in,

590
00:32:49,125 --> 00:32:52,916
our houses and will probably benefit from,

591
00:32:53,458 --> 00:32:56,791
an availability of biomarkers
at the level.

592
00:32:56,791 --> 00:32:59,791
And to certain extent,
you know, even with a WHOOP

593
00:32:59,875 --> 00:33:02,708
today,
you can have these digital biomarkers

594
00:33:02,708 --> 00:33:06,541
that are augmenting
your insights on your health.

595
00:33:06,541 --> 00:33:11,333
And I think this will happen over time
for things like protein for sure,

596
00:33:11,375 --> 00:33:15,583
which are challenging to measure
as you know, with the current technology,

597
00:33:15,583 --> 00:33:18,916
but they're becoming easier and easier
to measure with modern technologies.

598
00:33:19,208 --> 00:33:23,666
– And then you think to that, let's say
one of the barriers you have to go with like

599
00:33:23,833 --> 00:33:27,416
finding new ways of sequencing
or more easy ways of sequencing,

600
00:33:27,416 --> 00:33:31,250
or more handy ways of sequencing, right,
that there will be the future,

601
00:33:31,375 --> 00:33:33,625
how you envision it. 
– Totally, totally.

602
00:33:33,625 --> 00:33:36,500
That's why, we're investing,

603
00:33:36,500 --> 00:33:40,625
a billion three,
a billion four every year in R&D.

604
00:33:40,625 --> 00:33:44,041
That's Karen’s

605
00:33:44,041 --> 00:33:47,416
ward, she’s very tightly managing,

606
00:33:48,000 --> 00:33:51,958
the priority around,
everything that we spend in innovation.

607
00:33:51,958 --> 00:33:55,750
But, certainly that's the direction
we're driving towards.

608
00:33:55,750 --> 00:33:58,750
And I'm sure Karen
has some perspective on that.

609
00:33:59,291 --> 00:34:02,916
– No, I agree, I was laughing to myself
because I remember

610
00:34:02,916 --> 00:34:07,083
in the early days of the microbiome,
they wanted to put a digital detector

611
00:34:07,083 --> 00:34:10,666
in the toilet and so people could know
if they were sick.

612
00:34:10,666 --> 00:34:12,375
But but think about it, right, Cindy?

613
00:34:12,375 --> 00:34:16,625
I mean, imagine being able
to look at inflammation in a urine sample.

614
00:34:16,708 --> 00:34:19,250
It could become our future that, you know,

615
00:34:19,250 --> 00:34:24,041
you have some way to check at home
and this becomes a part of your lifestyle.

616
00:34:24,041 --> 00:34:26,250
So I, I do agree with that 100%.

617
00:34:26,250 --> 00:34:29,916
But in terms of our investment
in R&D and pushing the envelope

618
00:34:29,916 --> 00:34:33,625
and integrating cost company,
these are these opportunities.

619
00:34:33,625 --> 00:34:35,000
Again, you know, it's

620
00:34:35,000 --> 00:34:38,500
the things that wake you up in the morning
excited to go to work.

621
00:34:38,500 --> 00:34:40,208
We think about these opportunities.

622
00:34:40,208 --> 00:34:44,208
And I will tell you honestly that Gianluca

623
00:34:44,208 --> 00:34:49,666
and I think the proteomics space is
one of the especially bringing Olink in,

624
00:34:50,500 --> 00:34:54,083
is one of the biggest,
most exciting areas for us.

625
00:34:54,083 --> 00:34:56,208
So we don't advertise it all the time.

626
00:34:56,208 --> 00:34:57,166
But we are very,

627
00:34:58,291 --> 00:35:01,458
proud of the acquisition
and what it means for the company.

628
00:35:01,458 --> 00:35:04,166
– I love to hear it. 
– You are very welcome.

629
00:35:04,166 --> 00:35:04,833
Welcome on board.

630
00:35:04,833 --> 00:35:06,875
Very happy to have you on board. 
– Thank you.

631
00:35:06,875 --> 00:35:10,416
– It's been a year now, Sarantis,
and it's like, I've known you forever.

632
00:35:10,416 --> 00:35:12,333
– Yeah.

633
00:35:13,083 --> 00:35:15,333
– Yeah, we get under your skin. We get there. 

634
00:35:15,333 --> 00:35:16,958
– Yeah. We are, we are looking forward to.

635
00:35:16,958 --> 00:35:18,750
– It's very exciting.
– It's very exciting.

636
00:35:18,750 --> 00:35:22,416
It's very exciting to see that
the matching right with the omics pipeline

637
00:35:22,416 --> 00:35:23,375
that you’re having.

638
00:35:23,375 --> 00:35:26,875
And it's really clear, nice fit on that
because now it's a complete

639
00:35:27,000 --> 00:35:30,125
now it's a complete toolbox right
end to end for the customer

640
00:35:30,333 --> 00:35:32,625
from data generation
also to data interpretation.

641
00:35:32,625 --> 00:35:34,708
That's the beauty.
That's the beauty.

642
00:35:34,708 --> 00:35:35,625
– Yes. Correct.

643
00:35:36,083 --> 00:35:37,583
– Can I add one thing?

644
00:35:38,541 --> 00:35:39,583
I want to add one thing

645
00:35:39,583 --> 00:35:42,583
which is super important
because obviously,

646
00:35:43,083 --> 00:35:47,041
the Olink technology
as well as largely Mass Spec

647
00:35:47,041 --> 00:35:52,333
for untargeted protein, detection
and quantification,

648
00:35:53,375 --> 00:35:55,375
has been used in

649
00:35:55,375 --> 00:35:59,875
the translational and research space,
but one of the big unlock

650
00:35:59,875 --> 00:36:04,291
will be when those technologies
are getting to the clinics. And

651
00:36:05,041 --> 00:36:08,583
I think we have an interesting parallel
with what we did with Ion Torrent.

652
00:36:09,125 --> 00:36:13,166
We acquired the company back in 2011,
I believe,

653
00:36:13,875 --> 00:36:18,541
and now we are basically the enabler of,

654
00:36:19,375 --> 00:36:22,625
vast majority of clinical testing,

655
00:36:23,208 --> 00:36:26,166
that are next generation sequencing based,

656
00:36:26,166 --> 00:36:30,125
thanks to the fact that the team
has worked to streamline that technology.

657
00:36:30,125 --> 00:36:33,708
Now we have a fully integrated
and automated NGS,

658
00:36:34,541 --> 00:36:39,791
that is used for therapy selection,
with, you know, great products.

659
00:36:39,791 --> 00:36:42,916
We just announced that we got FDA approval

660
00:36:42,916 --> 00:36:46,250
for, our Genexus system. And,

661
00:36:47,458 --> 00:36:48,625
you know,

662
00:36:48,625 --> 00:36:52,166
a set of, panel and markers used for therapy selection.

663
00:36:52,166 --> 00:36:54,125
So it's incredibly exciting.

664
00:36:54,125 --> 00:36:56,000
It's been a long journey.

665
00:36:56,000 --> 00:36:58,333
But it's a journey that, we learned

666
00:36:58,333 --> 00:37:01,583
how to, go through and execute.

667
00:37:01,583 --> 00:37:05,375
And I do envision
the same journey on a shorter timeline

668
00:37:05,375 --> 00:37:09,125
because we learned a lot
over the last decade, 15 years.

669
00:37:09,625 --> 00:37:13,416
And I'm super excited thinking
at when we're going

670
00:37:13,416 --> 00:37:17,541
to see, proteomics,
into the clinics at scale.

671
00:37:18,041 --> 00:37:21,333
It will require obviously
content, technology, etc.

672
00:37:21,333 --> 00:37:25,708
but, it's, exciting to think about
when is going to happen.

673
00:37:26,041 --> 00:37:29,791
– And I think the what's critical
and we do this today with our focus panels

674
00:37:30,083 --> 00:37:33,041
is being able to turn over
those custom subsets

675
00:37:33,041 --> 00:37:36,750
of proteins that we already understand
exactly how they cross react together.

676
00:37:36,750 --> 00:37:39,250
We already understand how they play.

677
00:37:39,250 --> 00:37:43,958
And those, you know, authentication
steps of, you know, two antibodies and

678
00:37:44,208 --> 00:37:47,375
and one hybridization,
those that three factor authentication

679
00:37:47,375 --> 00:37:50,416
is really enabling this to happen quickly.

680
00:37:50,750 --> 00:37:52,541
And so I would encourage

681
00:37:52,541 --> 00:37:56,166
folks to keep an eye on this space
because we're already seeing, you know,

682
00:37:56,458 --> 00:38:00,000
there's over 700 references to the UK
Biobank.

683
00:38:00,250 --> 00:38:03,416
You know, foundation paper
that came from the pharma partners.

684
00:38:03,416 --> 00:38:05,958
That was in October of 2023.

685
00:38:05,958 --> 00:38:08,958
So lots of references by using those data,

686
00:38:09,125 --> 00:38:12,125
some of them just mining the data
for new insights.

687
00:38:12,875 --> 00:38:14,500
It's a rich source.

688
00:38:14,500 --> 00:38:17,833
– And if you don't trust a one factor
authentication

689
00:38:17,833 --> 00:38:21,666
for your digital needs,
why should you trust it for your health?

690
00:38:21,666 --> 00:38:22,125
– That’s true.

691
00:38:22,125 --> 00:38:24,541
– Exactly. 
– So use Olink.

692
00:38:24,541 --> 00:38:28,875
That's the only two factor authentication
at scale out there.

693
00:38:29,375 --> 00:38:32,125
– And antibodies are what we use
in therapies.

694
00:38:32,125 --> 00:38:32,375
Right.

695
00:38:32,375 --> 00:38:36,208
So I'm also excited
although much of it's behind closed doors.

696
00:38:36,500 --> 00:38:41,041
But when pharma are able to publish
on mechanistic insights

697
00:38:41,041 --> 00:38:45,708
from the, the therapeutic targets
that they're identifying, right.

698
00:38:45,708 --> 00:38:49,708
This is a big push for why
14 pharma partners are paying

699
00:38:49,708 --> 00:38:53,666
for 600,000 samples

700
00:38:53,666 --> 00:38:57,750
to be run, the entire cohort in the UK
Biobank.

701
00:38:57,750 --> 00:39:03,416
And I think that the mapping
of those causal pathways across different

702
00:39:03,416 --> 00:39:07,500
diseases is going to be a reference
that we will come back to for many years.

703
00:39:07,500 --> 00:39:08,875
It feels very good, Karen.

704
00:39:08,875 --> 00:39:11,791
It f feels like the GWAS revolution
over again.

705
00:39:11,791 --> 00:39:12,208
Right.

706
00:39:12,625 --> 00:39:18,333
It's like you say, it's just such a privilege 
to have a front row seat and a tiny,

707
00:39:19,458 --> 00:39:20,291
impact

708
00:39:20,291 --> 00:39:23,125
on where
this goes and where it will go next.

709
00:39:23,125 --> 00:39:27,250
– Well to be part of the team,
Cindy, we're all part of the team, right?

710
00:39:27,250 --> 00:39:29,375
– It's awesome. It's awesome.

711
00:39:29,375 --> 00:39:31,291
So I'm having the time of my life.

712
00:39:31,291 --> 00:39:32,958
I am having the time of my life.

713
00:39:32,958 --> 00:39:34,166
How about you, Sarantis?

714
00:39:34,166 --> 00:39:37,083
– Oh it's so great I mean, I'm
coming from the omics perspective, right.

715
00:39:37,083 --> 00:39:40,583
And being in a big family,
with the omics family coming together,

716
00:39:40,583 --> 00:39:42,125
which for me is the most exciting thing
ever.

717
00:39:42,125 --> 00:39:48,333
You know, looking forward to break into
clinics, looking for biomarkers and push and beat

718
00:39:48,375 --> 00:39:52,125
and convince FDA to have biomarkers
for clinical diagnostics.

719
00:39:52,166 --> 00:39:54,875
That's I think is the next step
I have to go through.

720
00:39:54,875 --> 00:39:57,000
– And, Cindy, one more plug.

721
00:39:57,000 --> 00:40:02,375
One more little comment to Miller
who is on our team sent me a list of about

722
00:40:02,375 --> 00:40:06,125
ten microbiome papers where they're using
Olink to look at inflammation.

723
00:40:06,375 --> 00:40:07,583
And doing that correlation.

724
00:40:07,583 --> 00:40:09,375
– Thanks for the reminder.

725
00:40:09,375 --> 00:40:14,625
– But it's just amazing how it's spanning
multiple different,

726
00:40:14,875 --> 00:40:16,291
areas of science, right.

727
00:40:16,291 --> 00:40:19,750
That you probably wouldn't have thought
about the connection originally.

728
00:40:19,916 --> 00:40:21,875
– That's right.
And we can put those in the show notes.

729
00:40:21,875 --> 00:40:23,125
So if folks are interested in that.

730
00:40:23,125 --> 00:40:27,208
I had just had a customer,
ask me specifically about that as well.

731
00:40:27,208 --> 00:40:30,541
Another person
who came from that microbiome.

732
00:40:30,541 --> 00:40:33,541
It’s still happening, this microbiome 
– Still trying.

733
00:40:33,541 --> 00:40:35,625
– revolution
where we're learning so much. Yeah.

734
00:40:35,625 --> 00:40:36,875
It's like they.

735
00:40:36,875 --> 00:40:38,541
I always think of them paying

736
00:40:38,541 --> 00:40:43,083
the biome is paying currency
like it's paying rent to live in our body.

737
00:40:43,083 --> 00:40:43,333
Right?

738
00:40:43,333 --> 00:40:46,208
By giving us these metabolites
like serotonin and things like this.

739
00:40:46,208 --> 00:40:50,791
Again, Gianluca and I,
I think both really love a good analogy.

740
00:40:51,625 --> 00:40:54,208
So, so final thoughts,

741
00:40:54,208 --> 00:40:57,416
we're just going to kind of,
wind down here.

742
00:40:57,416 --> 00:40:59,250
It's a pretty great place to end on.

743
00:40:59,250 --> 00:41:02,791
Gianluca, do you have some final thoughts
you'd like to leave our listeners with?

744
00:41:03,041 --> 00:41:04,541
– Absolutely.

745
00:41:04,541 --> 00:41:09,291
The future is bright and is bright,
thanks to the

746
00:41:09,875 --> 00:41:14,875
for us, 120 plus thousand colleagues
at the company showing up every day

747
00:41:15,208 --> 00:41:19,625
trying to create
those incredible innovation that,

748
00:41:20,541 --> 00:41:25,083
equally talented and incredibly important
customers and partners

749
00:41:25,083 --> 00:41:28,666
are using to actually transform
the way that,

750
00:41:29,250 --> 00:41:31,666
we identify early

751
00:41:31,666 --> 00:41:36,666
or fully, then ultimately identify
treatment and treat diseases that,

752
00:41:37,041 --> 00:41:40,125
today are either
not well treated or untreatable.

753
00:41:40,583 --> 00:41:44,083
And that's why
it is incredibly exciting.

754
00:41:44,083 --> 00:41:48,166
To do that well,
you actually need the right technology.

755
00:41:48,166 --> 00:41:50,458
Back to the analogy
of the self-driving car.

756
00:41:50,458 --> 00:41:51,875
You need the right sensors.

757
00:41:51,875 --> 00:41:55,041
You need the right orchestration,
information,

758
00:41:55,250 --> 00:41:59,583
and you want to rely on something
for your life.

759
00:41:59,583 --> 00:42:05,125
When you drive on a self-driving car or
when you actually drive through your life

760
00:42:05,125 --> 00:42:08,625
and you make medical decision,
you actually want to rely,

761
00:42:09,250 --> 00:42:12,958
on the best of the technologies
and our two factor

762
00:42:12,958 --> 00:42:13,916
authentication at Olink,
is something very special.

763
00:42:16,750 --> 00:42:19,750
And I think it has been,

764
00:42:19,916 --> 00:42:22,333
proven, testified by the adoption

765
00:42:22,333 --> 00:42:27,541
that we've seen from the UK Biobank study
as an example and the many partners

766
00:42:27,541 --> 00:42:30,916
in the pharma space
that now are working with us to create

767
00:42:30,916 --> 00:42:34,166
the next generation
of medicine and diagnostic.

768
00:42:34,500 --> 00:42:36,125
So it is incredibly exciting.

769
00:42:36,125 --> 00:42:41,500
It has been a great journey thus far,
and I can't wait for the next decade

770
00:42:41,500 --> 00:42:44,875
to play out
so that, together as an industry,

771
00:42:45,125 --> 00:42:48,833
we actually can truly transform
the way that, medicine works.

772
00:42:49,625 --> 00:42:50,333
– Beautiful.

773
00:42:50,333 --> 00:42:51,583
Karen?

774
00:42:51,583 --> 00:42:53,541
– Cindy,
I can't add anything more to that.

775
00:42:53,541 --> 00:42:55,000
I'm good.

776
00:42:55,000 --> 00:42:55,833
That was perfect.

777
00:42:55,833 --> 00:42:56,750
That was really good.

778
00:42:56,750 --> 00:43:00,083
So thank you again for having us.

779
00:43:00,083 --> 00:43:02,208
It's been really a lot of fun.

780
00:43:02,208 --> 00:43:04,500
– I’m so looking forward to it.

781
00:43:04,500 --> 00:43:08,125
So in the show notes,
I'll add some of the genetic corroboration

782
00:43:08,125 --> 00:43:10,416
of the Olink specificity
and also some mass spec

783
00:43:10,416 --> 00:43:13,125
corroboration of the Olink specificity
as well as Elisa.

784
00:43:13,125 --> 00:43:15,333
Right.
There's lots of ways to corroborate.

785
00:43:15,333 --> 00:43:18,500
You just have to be able to see
the protein in whatever matrix you're

786
00:43:18,500 --> 00:43:19,458
looking at.

787
00:43:19,458 --> 00:43:22,666
Any final words from you,
Sarantis – Oh, I mean, it's exciting.

788
00:43:22,666 --> 00:43:23,583
It's exciting times.

789
00:43:23,583 --> 00:43:26,708
And I mean looking forward
to break the barrier.

790
00:43:26,708 --> 00:43:27,666
Right.

791
00:43:27,666 --> 00:43:30,958
To make our world healthier, safer.

792
00:43:30,958 --> 00:43:33,125
Right. And, the best place to live.

793
00:43:33,125 --> 00:43:34,541
Thank you very much for your time.

794
00:43:34,541 --> 00:43:36,708
And it was great
honor to have you, both of you here.

795
00:43:36,708 --> 00:43:37,625
– Thank you, both.

796
00:43:37,625 --> 00:43:38,458
– Awesome.

797
00:43:38,458 --> 00:43:41,458
Well, just as a reminder,
if you want to reach out to us,

798
00:43:41,458 --> 00:43:45,541
we're at pip@olink.com
that stands for Proteomics in Proximity.

799
00:43:45,541 --> 00:43:46,875
We love to hear from you.

800
00:43:46,875 --> 00:43:51,125
We love to get feedback and questions
that you'd like to hear answered here.

801
00:43:51,708 --> 00:43:53,375
Thank you very much for tuning in.

802
00:43:55,708 --> 00:43:59,583
Well, that wraps up this episode 
of Proteomics in Proximity.

803
00:44:00,125 --> 00:44:04,208
Huge thanks to our guests and authors
of such impactful publications.

804
00:44:04,625 --> 00:44:07,208
I also want to thank you for tuning in.

805
00:44:07,208 --> 00:44:09,458
Really appreciate you being here.

806
00:44:09,458 --> 00:44:11,250
If you enjoyed the content of this

807
00:44:11,250 --> 00:44:15,125
episode, please think about sharing it
with friends or colleagues

808
00:44:15,125 --> 00:44:17,375
you think might be interested
in the content.

809
00:44:17,375 --> 00:44:21,458
In addition, if you'd be willing
to head over to Apple or Spotify

810
00:44:21,458 --> 00:44:24,916
or wherever you digest your podcasts
and give us a rating and review,

811
00:44:24,916 --> 00:44:26,958
this will help others find the podcast

812
00:44:26,958 --> 00:44:30,291
when they're searching for proteomics
or precision medicine podcasts.

813
00:44:30,541 --> 00:44:34,125
And mostly I want to say
we would love to hear from you.

814
00:44:34,291 --> 00:44:37,791
So we have a dedicated email address
pip@olink.com.

815
00:44:38,083 --> 00:44:39,250
Please reach out,

816
00:44:39,250 --> 00:44:43,208
let us know what you're interested
in hearing about what you care about

817
00:44:43,208 --> 00:44:47,250
and any feedback on the episodes
that we have already done so far.

818
00:44:47,541 --> 00:44:50,958
This is all about you,
and so we're really keen

819
00:44:50,958 --> 00:44:53,958
to make sure that we're meeting
what you like to hear about.

820
00:44:54,208 --> 00:44:56,333
Thank you so much and we'll see you soon.