Functional Genomics Team Leader @cnag_eu
Joined November 2017
- Tweets 769
- Following 1,249
- Followers 301
- Likes 18,504
6 Photos and videos
AnnaEsteveCodina retweeted
Primera sesión del #CongresoGenética26 destinada a las mejores comunicaciones orales.
Una sesión variada que traslada estudios genéticos aplicados a enfermedades raras, cáncer hereditario, asesoramiento genético en España o la exposición prenatal al fentanilo 🤰🧬
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AnnaEsteveCodina retweeted
Mejores comunicaciones orales en el #CongresoGenética26
10 ponencias donde se han acercado los últimos estudios y ensayos clínicos punteros en genética, asesoramiento genético y diagnóstico prenatal.
#EspecialidadesGenéticaYA
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🙌 Thrilled to contribute at CNAG!
@AEsteveCodina and Joan Pedrosa from our Functional Genomics Team analysed scRNA-seq & scTCR-seq in this research, which could pave the way for new gene therapy strategies for this rare immune disorder
#Genomics #RareDiseases #CNAG
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🚀New paper out!
Led by @VHIR with CNAG collaboration, the study reports an impressive case where the immune system spontaneously restored function in a patient with CD137 (4-1BB) deficiency, representing the first described somatic reversion in TNFRSF9
nature.com/articles/s41525-0…
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27 Nov 2025
Apply any of these PhD/ postdoc funding calls to work with rare disease multiomics, pangenome, episignatures, repetitive elements: cnag.eu/jobs/phd-postdoc-fel…
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📣The official programme for the 14th CNAG Symposium is live!
9⃣ Leading experts will share cutting-edge insights in #CancerGenomics, don’t miss it!
🗓️ Dec 16 | 09:00–16:15
📍 Auditori Antoni Caparrós, @PCB_UB (Barcelona)
👉 cnag.eu/events/14th-cnag-sym…
#CNAGSymposium #CNAG
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🌍Yesterday, our PhD student @tmontsay 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!
@AEsteveCodina
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🚨Webinar alert!
Today, our Functional Genomics Team Leader, @AEsteveCodina, will discuss the value of RNA-seq and long-read genome and methylome data in rare disease diagnosis
🗓️11:00 CEST
rwth.zoom.us/meeting/registe…
By @NGSCN_de & @UniklinikAachen
#Genomics #RareDiseases #CNAG
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💜 Even better news from the #Unicas_Hackathon!
5⃣ families have finally received a diagnosis after 48 hours of intense collaboration among international experts
A huge step forward for #RareDiseases and, most importantly, for these children
Proud to be part of this initiative!
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🙌¡Maratón por las enfermedades raras!
💜Ayer empezaba el primer Únicas Hackathon, un encuentro de clínicos, investigadores y genetistas para hallar el diagnóstico de 12 casos pediátricos en 48 horas
🧬Como colaboradores, nuestro equipo fue hasta Murcia para ayudar a la causa
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📢New paper out in @NatureGenet!
✨CNAG coordinates the Solvathons, a groundbreaking pan-European initiative for rare disease diagnosis
@Solve_RD launched these interdisciplinary workshops, which have led to 100 new diagnoses for rare disease families
📎cnag.eu/news/cnag-coordinate…
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🙌New advances on rare diseases!
Within the @Solve_RD, @PacBio HiFi long-read whole-genome sequencing has proven instrumental in uncovering previously undetectable genetic variants, leading to new diagnoses
genome.cshlp.org/content/35/…
#RareDiseases #CNAG @genomeresearch @ERDERA_org
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🚨New job offer!
➡️Join the Functional Genomics Team at CNAG as a Bioinformatician to work on the SEED-ALS Spain project, a national initiative focused on understanding and treating Amyotrophic Lateral Sclerosis (ALS)
🗓️ Apply by 30 September
🔗 cnag.eu/jobs
#CNAG
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📢We’re hiring!
Join our team at CNAG and help advance genomics research!
Check out our new positions:
➡️Bioinformatician (Functional Genomics Team)
➡️PhD Student - Computational Biologist (Single Cell Team)
🔗cnag.eu/jobs
#Jobs #Hiring #Genomics #ResearchJobs
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🌍 Today is World RNA Day!
Discover with our Functional Genomics Team Leader, @AEsteveCodina, 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
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📢New paper in Neuromuscular disorders (@WorldMuscleSoc)!
🧬A study helped identify a new genetic variant in the TNNT3 gene causing a rare muscle disorder in two siblings, thanks to a multi-omics approach (genomics and transcriptomics)
📎nmd-journal.com/article/S096…
#RareDiseases
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AnnaEsteveCodina retweeted
10 Jun 2025
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Low MALAT1 levels (e.g., <1% of median) are reliable indicators of damaged cells or low-quality nuclei in snRNA-seq.
read 10x Q&A kb.10xgenomics.com/hc/en-us/…
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AnnaEsteveCodina retweeted
10 Jun 2025
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In Tabula Muris and Tabula Sapiens, MALAT1 expression was tightly correlated with nuclear RNA content and intronic fractions. bmcgenomics.biomedcentral.co…
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AnnaEsteveCodina retweeted
Best Poster in Clinical Research
Rebeka Luknárová, Munich, Germany
P16.006.A - "Harmonized framework for RNA-seq-based rare disease diagnostics in a pan-continental consortium - Solve-RD"
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🙌 Really excited about this recognition!
Congratulations to our partners from @TU_Muenchen — Rebeka Luknárová, @vaym88, and Julien Gagneur — together with our Functional Genomics Team Leader at CNAG, @AEsteveCodina, and @Solve_RD
#research #eshg2025 #bestposter
Best Poster in Clinical Research
Rebeka Luknárová, Munich, Germany
P16.006.A - "Harmonized framework for RNA-seq-based rare disease diagnostics in a pan-continental consortium - Solve-RD"
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