Anna Esteve Codina
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annaesteveco.bsky.social
Anna Esteve Codina
@annaesteveco.bsky.social
Functional Genomics Team Leader @CNAG 🧬💻🔎 omics, rare diseases, single-cell, long-reads, transposons.
Reposted by Anna Esteve Codina
🌍Yesterday, our PhD student @tmontsay.bsky.social from the Functional Genomics Team presented his poster at #EMBOMobileGenome on 'A Comprehensive Annotation of Conserved Protein Domains in Human Endogenous Retroviruses'

🙌 Excellent work and insightful discussions!
@annaesteveco.bsky.social #CNAG
November 6, 2025 at 9:19 AM
Reposted by Anna Esteve Codina
🚨Webinar alert!
Today, our Functional Genomics Team Leader,
@annaesteveco.bsky.social, will discuss the value of RNA-seq & long-read genome and methylome data in rare disease diagnosis

🗓️ 11:00 CEST
rwth.zoom.us/meeting/regi...

By Next Generation Sequencing Competence Network
#RareDiseases
October 16, 2025 at 7:12 AM
Reposted by Anna Esteve Codina
📢 New paper out in @natgenet.nature.com!
✨ CNAG coordinates the Solvathons, a groundbreaking pan-European initiative for rare disease diagnosis

Solve-RD launched these interdisciplinary workshops, which have led to over 100 new diagnoses for rare disease families

🔗 www.cnag.eu/news/cnag-co...
September 9, 2025 at 9:38 AM
Reposted by Anna Esteve Codina
🌍 Today is World RNA Day!
Discover with our Functional Genomics Team Leader,
@annaesteveco.bsky.social, why RNA is a vital biological key: essential for advancing research in cancer, rare diseases

🌟At CNAG, we study RNA to improve people's health and quality of life

#RNADay #RNA #CNAG #Genomics
August 1, 2025 at 10:39 AM
Reposted by Anna Esteve Codina
🧵 1/
🚨 New preprint alert!

Excited to share my first PhD paper, supervised by @annaesteveco.bsky.social at @cnag-eu.bsky.social:

📄 A Comprehensive Annotation of Conserved Protein Domains in Human Endogenous Retroviruses
📄 Preprint: www.biorxiv.org/content/10.1...

🧬 Read on for the dataset & code!
A Comprehensive Annotation of Conserved Protein Domains in Human Endogenous Retroviruses
Human endogenous retroviruses (HERVs) occupy nearly 8% of the human genome, yet their protein-coding potential remains largely unexplored. Like their exogenous counterparts, HERVs derive from ancestra...
www.biorxiv.org
July 31, 2025 at 6:21 AM
Reposted by Anna Esteve Codina
📢New paper out in Frontiers in Immunology!
🔎A study by IRTA, IRTA-CReSA, @uab.cat and CNAG explores how heat-inactivated bacterium Rothia nasimurium boosts pig macrophage immunity — helping fight major pig viruses, such as PRRSV & ASFV

www.frontiersin.org/journals/imm...
#Sustainability #CNAG
Frontiers | Inactivated Rothia nasimurium promotes a persistent antiviral immune status in porcine alveolar macrophages
Globalization has increased the incidence of infectious diseases in livestock, further aggravated by the reduction of antibiotic usage. To minimize the resul...
www.frontiersin.org
June 23, 2025 at 7:50 AM
Reposted by Anna Esteve Codina
7/
In Tabula Muris and Tabula Sapiens, MALAT1 expression was tightly correlated with nuclear RNA content and intronic fractions. bmcgenomics.biomedcentral.com/articles/10...
High content of nuclei-free low-quality cells in reference single-cell atlases: a call for more stringent quality control using nuclear fraction - BMC Genomics
The advent of droplet-based single-cell RNA-sequencing (scRNA-seq) has dramatically increased data throughput, enabling the release of a diverse array of tissue cell atlases to the public. However, we will show that prominent initiatives such as the Human Cell Atlas [1], the Tabula Sapiens [2] and the Tabula Muris [3] contain a significant amount of contamination products (frequently affecting the whole organ) in their data portals due to suboptimal quality filtering. Our work addresses a critical gap by advocating for more stringent quality filtering, highlighting the imperative for a shift from existing standards, which currently lean towards greater permissiveness. We will show the importance of incorporating cell intronic fraction in quality control -or MALAT1 expression otherwise- showcasing its informative nature and potential to elevate cell atlas data reliability. In summary, here, we unveil the hidden intronic landscape of every tissue and highlight the importance of more rigo
bmcgenomics.biomedcentral.com
June 10, 2025 at 1:45 PM
Reposted by Anna Esteve Codina
🌟Still buzzing from #eshg2025!
7,000 attendees from 94 countries gathered in Milan — our CNAG team was spreading the word about our mission: applying genomics to improve health

🙏Thanks to @eshg.bsky.social & all pushing the boundaries of Human Genetics — see you in Gothenburg!🇸🇪
#GenomicsIsInOurDNA
May 29, 2025 at 6:46 AM
Reposted by Anna Esteve Codina
💪 What a dream team we’ve got at CNAG for #eshg2025 — our super project managers, the Human Genetics and the Functional Genomics Team!

😎And just look how good we look in our new t-shirts…
CNAG is giving it all, once again!
📍Find us at booth 382

#GenomicsIsInOurDNA #eshg #milan
May 25, 2025 at 9:10 AM
Reposted by Anna Esteve Codina
🗣️Impressive talk by our Data Analyst Gemma Bullich at #eshg2025!

🧬“Increased diagnosis rate in rare diseases through iterative re-analysis and multi-omics data integration” (C24.01)

👏 So proud of our Human Genetics team. Well done, Gemma!
#Genomics #RareDiseases #MultiOmics #GenomicsIsInOurDNA
May 26, 2025 at 8:54 AM
Reposted by Anna Esteve Codina
🙌 Really excited about this recognition!

Congratulations to our partners from @tum.de — Rebeka Luknárová, Vicente Yépez, and Julien Gagneur — together with our Functional Genomics Team Leader at CNAG, @annaesteveco.bsky.social, and Solve RD

#research #eshg2025 #bestposter
May 27, 2025 at 1:55 PM
Reposted by Anna Esteve Codina
🔥Non-stop on the last day of #eshg2025!

🗣️This morning we joined the oral presentation of our partner Vicente Yepez (Technical University Munich): 'Rare Disease Solvathons – the power of multi-omics data integration'

🙌Truly inspiring work!
#RareDiseases #CNAG #GenomicsIsInOurDNA #Research
May 27, 2025 at 9:56 AM
Reposted by Anna Esteve Codina
📍Don’t miss us at the Sequencing Square, Hall 4!
🗓️Monday, 26 May at 11:00

🧬Our Functional Genomics Team Leader at CNAG, @annaesteveco.bsky.social‬, is presenting the poster “Integrative multi-omics for undiagnosed Rare Diseases (Omics-RD)”

#eshg2025 #RareDiseases #GenomicsIsInOurDNA #CNAG
May 26, 2025 at 8:50 AM
Reposted by Anna Esteve Codina
🧬Great presentation by our Functional Genomics Team Leader, @annaesteveco.bsky.social, at #eshg2025!

🗣️She showcased our work on “Integrative multi-omics for undiagnosed Rare Diseases (Omics-RD)”

👏 Congratulations, Anna, and well done to the team behind this project!
#RareDiseases #CNAG
May 26, 2025 at 9:43 AM
Reposted by Anna Esteve Codina
🙌 What a great day!

🧑‍🔬👨‍🔬 Today we had the pleasure of meeting our partners Vicente Yepez (OmicsDiscoveries) and Ana Topf (@newcastleuni.bsky.social) at #eshg2025 — proud to keep advancing rare disease research together!

It’s always a pleasure to connect and exchange ideas!
#GenomicsIsInOurDNA #CNAG
May 24, 2025 at 1:35 PM
Reposted by Anna Esteve Codina
📷 Another moment we’re keeping from #eshg2025:
Yesterday we had the pleasure of meeting many of our @erdera.bsky.social‬ Diagnostic Research Workstream partners in Milan

🧩We're proud to be part of this committed consortium working to advance rare disease diagnostics

#RareDiseases #HorizonEurope
May 25, 2025 at 3:30 PM
Reposted by Anna Esteve Codina
👥This is us!

The CNAG team at #eshg2025: our Project Managers Elena Vila and Francesc Bou, Clinical Genomics Manager @lmatalonga.bsky.social‬, Functional Genomics Leader @annaesteveco.bsky.social‬, Data Analysts Steve Laurie and Gemma Bullich, and our Director Ivo Gut

🗓️Book a meeting with us!
May 25, 2025 at 12:00 PM
Reposted by Anna Esteve Codina
🎉Ready for the poster sessions at #eshg2025!

@annaesteveco.bsky.social, our Functional Genomics Team Leader at CNAG, will present: “Integrative multi-omics for undiagnosed Rare Diseases (Omics-RD)”

🗓️Sunday, 25 May at 13:00-14:00
🗓️Monday, 26 May at 11:00
📌Exhibition Hall

#GenomicsIsInOurDNA
May 24, 2025 at 10:10 AM
Reposted by Anna Esteve Codina
🔬Ayer culminaba el proyecto sobre cáncer colorrectal en adolescentes y adultos jóvenes, financiado por @contracancerinv.bsky.social y coordinado por Sergi Castellví (@idibaps.bsky.social)

La Dr. @annaesteveco.bsky.social acudió desde CNAG, que ha aplicado RNA-seq para identificar su mutación causal
May 15, 2025 at 11:16 AM
Reposted by Anna Esteve Codina
💜Today, we celebrate that talent, dedication, and commitment know no gender. At CNAG, equity and inclusion are in our DNA, creating an environment where everyone’s potential is recognised and valued

#WomensDay #DiversityMatters #8M #8M2025 #Diadelamujer #DiadelaDona #CNAG
March 8, 2025 at 9:20 AM
Reposted by Anna Esteve Codina
And this is happening today. @vevotherapeutics.bsky.social and @arcinstitute.org Institute are joining forces to release Tahoe100M and scBaseCamp (>200M AI-curated cells from Arc). Arc’s Virtual Cell Atlas launches as the largest single cell data repository!
arcinstitute.org/news/news/ar...
Arc Virtual Cell Atlas launches, combining data from over 300 million cells | Arc Institute
Arc Institute today launched the Arc Virtual Cell Atlas, a growing resource for computation-ready single-cell measurements, starting with data from over 300 million cells. The initial release of the A...
arcinstitute.org
February 25, 2025 at 1:25 PM
Reposted by Anna Esteve Codina
🌟Great News: CNAG is now on BlueSky!
🚀From Barcelona to the world, we’re bringing you the latest in genomics!

Stay tuned for breaking news, cutting-edge technologies, groundbreaking research, and upcoming events

🔗https://www.cnag.eu
#Genomics #Innovation #Research #BlueSky #CNAG
a blue sky with a butterfly and the word bluesky on it
ALT: a blue sky with a butterfly and the word bluesky on it
media.tenor.com
February 19, 2025 at 1:33 PM
🧬Check our asms tool 🛠, fast alternative to detect allele-specific methylation & imprinting using long-reads without the need of phasing www.biorxiv.org/content/10.1...
ASMS: finding allele specific methylation in human genomes without phasing
Motivation: Allele-specific methylation (ASM) refers to differential DNA methylation patterns between two alleles at a given locus. This phenomenon is often driven by genetic variants, such as single ...
www.biorxiv.org
December 23, 2024 at 12:42 PM
Reposted by Anna Esteve Codina
Also filter on markers like MALAT1, cell intronic mapping reads cf. bmcgenomics.biomedcentral.com/articles/10....
December 13, 2024 at 2:42 PM
Huge effort from @anaconesa.bsky.social at @scb.iec.cat comparing long-read RNA technologies @pacbio.bsky.social @nanoporetech.com and softwares #sqanti3, #bambu, #talon, #isoquant, for isoform discovery, still challenging to disentangle real biology from artefacts
December 13, 2024 at 12:50 PM