Shubhankar Londhe's Avatar

Shubhankar Londhe

@slondhe.bsky.social

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

168 Followers  |  369 Following  |  3 Posts  |  Joined: 14.11.2024
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Posts by Shubhankar Londhe (@slondhe.bsky.social)

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

14.10.2025 21:56 β€” πŸ‘ 3    πŸ” 0    πŸ’¬ 0    πŸ“Œ 0
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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.

14.10.2025 15:40 β€” πŸ‘ 8    πŸ” 3    πŸ’¬ 0    πŸ“Œ 1
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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...

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

09.09.2025 11:42 β€” πŸ‘ 5    πŸ” 1    πŸ’¬ 0    πŸ“Œ 0
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[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

24.07.2025 09:26 β€” πŸ‘ 42    πŸ” 21    πŸ’¬ 1    πŸ“Œ 2
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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

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...

23.07.2025 08:35 β€” πŸ‘ 10    πŸ” 1    πŸ’¬ 0    πŸ“Œ 0

@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
πŸ“… July 21 |πŸ“ Poster A-312

19.07.2025 17:33 β€” πŸ‘ 4    πŸ” 4    πŸ’¬ 1    πŸ“Œ 0

Join us for our next Kipoi Seminar with Katherine Pollard, Gladstone Institute of Data Science & Biotechnology,UCSF, Biohub
@gladstoneinst.bsky.social @czbiohub.bsky.social
πŸ‘‰Human variant interpretation with sequence-to-activity models
πŸ“…Wed June 4,5:30pm CET🧬 kipoi.org/seminar/πŸ¦‹@kipoizoo.bsky.social

28.05.2025 13:06 β€” πŸ‘ 4    πŸ” 4    πŸ’¬ 0    πŸ“Œ 1

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).

25.05.2025 10:33 β€” πŸ‘ 2    πŸ” 0    πŸ’¬ 0    πŸ“Œ 0

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 cellsβ€”analyzed in 5,000 UK Biobank participants

25.05.2025 07:40 β€” πŸ‘ 10    πŸ” 3    πŸ’¬ 0    πŸ“Œ 0
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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...

06.03.2025 21:04 β€” πŸ‘ 11    πŸ” 3    πŸ’¬ 0    πŸ“Œ 0
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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...

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...

19.02.2025 08:15 β€” πŸ‘ 14    πŸ” 5    πŸ’¬ 1    πŸ“Œ 1

Join us for our next Kipoi Seminar with with Pedro Tomaz da Silva @pedrotomazdasilva.bsky.social @gagneurlab.bsky.social @TU_Muenchen!
πŸ‘‰Nucleotide dependency analysis of DNA language models reveals genomic functional elements
πŸ“…Wed Feb 5, 5:30pm CET
🧬https://kipoi.org/seminar/
πŸ¦‹kipoizoo.bsky

03.02.2025 16:11 β€” πŸ‘ 10    πŸ” 6    πŸ’¬ 0    πŸ“Œ 1

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.

23.12.2024 09:15 β€” πŸ‘ 18    πŸ” 7    πŸ’¬ 0    πŸ“Œ 0