Happy to see our new paper on #WNV out: Cocirculation of endemic and recently introduced West Nile Virus lineage 1 clades in Southern Spain t.co/2PoAjs9EJ1

www.instagram.com/p/DVCEOegiDvP/

¿Tu receta médica entiende a tu ADN? Farmacogenómica o lo que nos enseñan los genes sobre nuestra capacidad para asimilar y tolerar los medicamentos

open.substack.com/pub/joaquind...

Tu ADN puede anticipar parte de tu salud futura, pero no por “un gen”: muchas enfermedades comunes tienen riesgo poligénico (PRS/PGS). Lo relevante: la población importa y por eso es clave el nuevo SpPGS, el Atlas del PRS/PGS de la población española t.co/ksnAJ2S7mQ

#siega #epidemiologiagenomica #bioinformatica #saludpublica #onehealth #genomica #wgs #postdoc #andalucia #investigacion | Joaquin Dopazo ¿Quieres hacer tu tesis en genómica bacteriana dentro de una de las iniciativas más ambiciosas de vigilancia genómica de patógenos del pais para convertir sus secuencias genómicas en decisiones de sal...

El equipo de SIEGA busca estudiantes para hacer tesis en genómica bacteriana. Detalles: www.linkedin.com/posts/joaqui...

El servidor colaborativo de variación genética de la población española (CSVS) Por qué las frecuencias locales cambian el diagnóstico, la investigación… y la prescripción

Empezamos el año hablando del servidor colaborativo de variación genética de la población española (CSVS) joaquindopazo.substack.com/p/el-servido...

El 'CSI' de los microbios: 4 revelaciones de SIEGA, el sistema que vigila nuestra salud en Andalucía Del misterio de una intoxicación a la certeza genómica

Un brote no se resuelve con intuición: se resuelve estudiando el ADN del microbio.
A finales de año, #SIEGA ya integra 4.037 genomas y conecta hospital-alimento-ambiente (#OneHealth).
Trazabilidad, vigilancia genómica y alerta temprana frente a AMR.
👉 joaquindopazo.substack.com/p/el-csi-de-...

The Spanish Polygenic Score reference distribution: a resource for personalized medicine - European Journal of Human Genetics European Journal of Human Genetics - The Spanish Polygenic Score reference distribution: a resource for personalized medicine

The SpPGS Atlas repository of PGS from the Spanish population, derived from the #CSVS 🧬
@xdopazo.bsky.social

www.nature.com/articles/s41...

Revolutionizing Healthcare // Engagement Sessons // van der Schaar Lab Revolutionizing Healthcare will target the the healthcare community and focus on challenges and opportunities in clinical application of machine learning.

Looking forward to participating in the next session AI for Discovery [Inspiration Exchange] vanderschaar-lab.com/engagement-s... organised by Mihaela VanDerSchaar (Cambridge Univ, The Alan Turing Inst.) #ArtificalIntelligence in #healthcare

The Spanish Polygenic Score reference distribution: a resource for personalized medicine @xdopazo.bsky.social idp.nature.com/authorize?re...

PGS adjusted to the Spanish population are available at the #CSVS csvs.clinbioinfosspa.es along with more useful information on the genomic variability of the Spanish population

The Spanish Polygenic Score reference distribution: a resource for personalized medicine - European Journal of Human Genetics European Journal of Human Genetics - The Spanish Polygenic Score reference distribution: a resource for personalized medicine

Happy to see our paper on "The Spanish Polygenic Score reference distribution: a resource for personalized medicine" out nature.com/articles/s41... this is a collaborative effort of the CIBERER, Navarrabiomed and other groups across Spain @ibis-investigacion.bsky.social

A detailed descrition of our successful "Genomic Surveillance Circuit for Emerging Viral Pathogens" in Andalusia has been published: www.mdpi.com/2076-2607/13... @ibis-investigacion.bsky.social

First autochthonous transmission of West Nile virus (WNV) lineage 2 to humans in Spain West Nile Virus (WNV) lineage 2, primarily endemic to parts of Africa and Europe, has recently emerged as a public health concern in new geographic re…

Our Circuit of Genomic Surveillance of Pathogens detected the " First autochthonous transmission of West Nile virus (WNV) lineage 2 to humans in Spain" See details in the publication: www.sciencedirect.com/science/arti... @ibis-investigacion.bsky.social

#seis #inforsalud25 #saluddigital #innovaciónsanitaria | SEIS, Sociedad Española de Informática de la Salud #SEIS #Inforsalud25 #SaludDigital #InnovaciónSanitaria XXVIII Congreso Nacional de Informática de la Salud - Sesión Debate 7 “Medicina Preventiva y Predictiva: Anticipando el Futuro de la Salud”- D. J...

Interesante mesa redonda sobre medicina predictiva en Infors@lus de la SEIS. Hablé de datos de mundo real y predictores de cáncer en población general. www.linkedin.com/feed/update/...

Metatranscriptomic analysis reveals gut microbiome bacterial genes in pyruvate and amino acid metabolism associated with hyperuricemia and gout in humans - Scientific Reports Scientific Reports - Metatranscriptomic analysis reveals gut microbiome bacterial genes in pyruvate and amino acid metabolism associated with hyperuricemia and gout in humans

Happy to see our collaborative paper "Metatranscriptomic analysis reveals gut microbiome bacterial genes in pyruvate and amino acid metabolism associated with hyperuricemia and gout in humans" already published www.nature.com/articles/s41...

Esta tarde hablaré en #ENZOEM de SIEGA, la Plataforma de vigilancia genómica de patógenos que hemos desarrollado con más de 3000 genomas de 7 especies bacterianas #onehealth y clínicas + #westnilefever y otros www.clinbioinfosspa.es/projects/sie...

En ENZOEM con Margarita del Val hablando de la Plataforma Interdisciplinaria de salud global #onehealth

Un año más empieza el curso PANMEP , el Diploma de experto en medicina personalizada y de precisión medicinaprecisionandalucia.easp.es Medicina genómica, diagnóstico de precisión, inteligencia artificial y más temas que están transformando la medicina

Check out the upcoming 9th Disease Maps Community Meeting organised by the Biomechanics Research Unit, KU Leuven and University of Liège and hosted at the KU Leuven, Leuven - Belgium disease-maps.io/DMCM2025/ @dasciinst.bsky.social @mlsb-borgwardt.bsky.social

Pues un año más ya están aquí de nuevo, las Jornadas Andaluzas de BioInformática #JABI25 jabi2025.uma.es 12-14 Mayo 2025 en Málaga. Podeis ver fechas clave y detalles en la página de web. Os esperamos en Málaga. @mgclaros.bsky.social @jpflorido.bsky.social @dasciinst.bsky.social

👉 Researchers world-wide take the CAMDA Challenge (contest.camda.info) - compete with the best in an open-ended data analysis contest and bring home the Camda Trophy!

Paweł P. Łabaj on LinkedIn: #camda2025 #camda #camda 📢 The Call for Contributions to #CAMDA2025 is now open! CAMDA (www.camda.info) is a full conference track at ISMB/ECCB (https://lnkd.in/daFA5Pg3). 👉…

www.linkedin.com/feed/update/...

The Call for Contributions to #CAMDA2025 is now open!

CAMDA (www.camda.info) is a full conference track at ISMB/ECCB (lnkd.in/daFA5Pg3).

@theevidencebase.bsky.social @loucerac.bsky.social @mlsb-borgwardt.bsky.social

Real world data analysis of venous thromboembolism, adverse major cardiovascular events, neoplasia and serious infections in ulcerative colitis patients Venous thromboembolism (VTE), major adverse cardiovascular events (MACE), neoplasia, and serious infections are significant complications associated with Immune-mediated inflammatory diseases. Actuall...

See our preprint on Real world data analysis of venous thromboembolism, adverse major cardiovascular events, neoplasia and serious infections in ulcerative colitis patients
www.medrxiv.org/content/10.1... in @medrxivpreprint.bsky.social Generating evidence from #RealWorldData

High impact of the genetic diagnosis. This information to evaluate familial implications, such as identification of at-risk family members, guidance for reproductive decisions or treatment recommendations. genetic data guided informed clinical decisions for 1084 patients across many disease groups.

Assisted Variant prioritization with the MMP application, developed bythe Platform of Computational Medicine. Improved and faster disgnosis rate, with a gradual expansion of the number of rare diseases analysed.

A genomic strategy for precision medicine in rare diseases: integrating customized algorithms into clinical practice - Journal of Translational Medicine Background Despite the use of Next-Generation Sequencing (NGS) as the gold standard for the diagnosis of rare diseases, its clinical implementation has been challenging, limiting the cost-effectivenes...

Finally our collaborative paper "A genomic strategy for precision medicine in rare diseases" is out translational-medicine.biomedcentral.com/articles/10.... An innovative strategy for diagnosis of #RareDisease patients, with more than 6,500 individuals analysed in the last years.

Andalucía participa en la creación de una red internacional de inteligencia artificial en Ciencias de la Salud El director de la Plataforma de Medicina Computacional de la Fundación Progreso y Salud es uno de los miembros fundadores de esta estructura orientada a la formación

Andalucía está presente en la Red Internacional de Inteligencia Artificial en Ciencias de la Salud (AI-LIFE) juntadeandalucia.es/presidencia/...

Don't miss the seminar "Revolutionizing Healthcare with AI: From Copilots to Clinical Discovery" by Mihaela van der Schaar, a leading authority in machine learning, artificial intelligence, and medicine. Next Tuesday 14th in the Salon de Grados, ETSI, Universidad de Sevilla