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Shubhankar Londhe

@slondhe.bsky.social
187 followers 394 following 3 posts

PhD student @gagneurlab.bsky.social (TU Munich and Helmholtz Munich). Interested in rare variant genetics. shubhankarlondhe.github.io

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Reposted by Shubhankar Londhe
Pedro Beltrao @pedrobeltrao.bsky.social · 23/06/2026
Not being able to access the @ukbiobank.ac.uk is becoming a significant issue for a PhD student in our group and I can only imagine this is mirrored in many other places. It would be fantastic to at least have a timeline we could work with.
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Shubhankar Londhe @slondhe.bsky.social · 14/10/2025
Why be satisfied with coding variant gene impairments? Check out Eva’s poster to learn how we scale DeepRVAT to the WGS UKBiobank. It’s been great fun being a part of this project! #ASHG25
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Shubhankar Londhe @slondhe.bsky.social · 14/10/2025
Excited to share UKBBGym at #ASHG25, a new benchmark for variant effect predictors using WGS, proteomics and phenotypes from 500K UKBiobank participants. Stop by for insights on the impact of non-coding variants and how computational scores stack up against exp assays. Poster 5022W, Wed 2:30-4:30.
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Reposted by Shubhankar Londhe
Gagneur lab @gagneurlab.bsky.social · 09/09/2025
The Solvathons have been one of our most exciting research community experiences: Hands-on, effective – solving real cases during the events, and multidisciplinary – from clinicians to bioinformaticians. Thumbs up to the SolveRD community. Looking for more now with @erdera.bsky.social rdcu.be/eFaqO
rdcu.be
The Solve-RD Solvathons as a pan-European interdisciplinary collaboration to diagnose patients with rare disease
Nature Genetics - This Perspective presents the Solve-RD Solvathon model, an innovative, pan-European framework uniting clinical and bioinformatics experts to diagnose rare diseases through...
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Reposted by Shubhankar Londhe
Samarendra Pani @samarendra-pani.bsky.social · 24/07/2025
[1/8] *New Open-Access Long Read Resource*. We sequenced 1,019 genomes from the 1000 Genomes Project sample cohort using @nanoporetech.com long-read sequencing (LRS) to median 17x coverage. Publication at go.nature.com/4ffPb8f. @hhu.de @crg.eu @embl.org @impvienna.bsky.social
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Reposted by Shubhankar Londhe
Gagneur lab @gagneurlab.bsky.social · 23/07/2025
Today at 12:20 in the HIT-Seq COSI, @lauradmartens.bsky.social Laura Martens will present her results on spatial chromatin accessibility data deconvolution #ISMBECCB2025. Great collab with Sarah Ouologuem and @fabiantheis.bsky.social Proceedings paper: doi.org/10.1093/bioi...
doi.org
Spatial transcriptomics deconvolution methods generalize well to spatial chromatin accessibility data
AbstractMotivation. Spatially resolved chromatin accessibility profiling offers the potential to investigate gene regulatory processes within the spatial c
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Reposted by Shubhankar Londhe
Stegle Lab @steglelab.bsky.social · 19/07/2025
@thbec.bsky.social is going to share preliminary results on Meta-DeepRVAT, a new approach for deep learning based meta-analysis improving the power of rare variant association studies using population scale external control cohorts. #MLCSB 📅 July 21 |📍 Poster A-312
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Reposted by Shubhankar Londhe
Kipoi @kipoizoo.bsky.social · 28/05/2025
Join us for our next Kipoi Seminar with Katherine Pollard, Gladstone Institute of Data Science & Biotechnology,UCSF, Biohub @gladstoneinst.bsky.social @czbiohub.bsky.social 👉Human variant interpretation with sequence-to-activity models 📅Wed June 4,5:30pm CET🧬 kipoi.org/seminar/🦋@kipoizoo.bsky.social
kipoi.org
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Shubhankar Londhe @slondhe.bsky.social · 25/05/2025
Excited to present at #eshg2025. Catch my talk on improving rare variant association studies using functional gene embeddings, on Monday at 11:45am (C26.06).
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Reposted by Shubhankar Londhe
Eva Holtkamp @evaholtkamp.bsky.social · 25/05/2025
Excited to be back at #eshg2025! Come by my poster today to check out fresh results on how rare high impact variants influence gene expression across immune cells—analyzed in 5,000 UK Biobank participants
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Reposted by Shubhankar Londhe
Gagneur lab @gagneurlab.bsky.social · 06/03/2025
Tomorrow Johannes Hingerl @johahi.bsky.social gives a talk on scooby at #probgen25. Enjoy learning in the legendary CSHL auditorium how to model RNA-seq and ATAC-seq profiles in individual cells from half a megabase of genomic sequence. Preprint: doi.org/10.1101/2024...
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Reposted by Shubhankar Londhe
Gagneur lab @gagneurlab.bsky.social · 19/02/2025
Excited to share that PROTRIDER, our method to call outliers on mass spectrometry-based proteomics data, is out now!! #proteomics #massspectrometry #raredisease doi.org/10.1101/2025...
doi.org
PROTRIDER: Protein abundance outlier detection from mass spectrometry-based proteomics data with a conditional autoencoder
Motivation Detection of gene regulatory aberrations enhances our ability to interpret the impact of inherited and acquired genetic variation for rare disease diagnostics and tumor characterization. Wh...
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Reposted by Shubhankar Londhe
Kipoi @kipoizoo.bsky.social · 03/02/2025
Join us for our next Kipoi Seminar with with Pedro Tomaz da Silva @pedrotomazdasilva.bsky.social @gagneurlab.bsky.social @TU_Muenchen! 👉Nucleotide dependency analysis of DNA language models reveals genomic functional elements 📅Wed Feb 5, 5:30pm CET 🧬https://kipoi.org/seminar/ 🦋kipoizoo.bsky
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Reposted by Shubhankar Londhe
Gagneur lab @gagneurlab.bsky.social · 23/12/2024
Hey reg genomics folks, here is our little x-mas present: Flashzoi. Borzoi. Just as good. 3x faster. Thumbs up to @johahi.bsky.social for the great initiative, conception & implementation. Big thanks to Johannes Linder, David Kelley and colleagues to have created Borzoi and shared it freely.
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