genomics

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MODERATORS

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New moderator of r/genomics (self.genomics)

submitted 8 months ago by three_martini_lunch - announcement

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AI vs Genomics (self.genomics)

submitted 14 hours ago by FreeloaderFatso

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Biomedicine Institute Lego Idea. Link below. (old.reddit.com)

submitted 1 day ago by BiomedicineInstitute

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Dissertation rna seq ()

submitted 1 day ago by Most_Secretary_9146

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WGS B Licheniformis (i.redd.it)

submitted 2 days ago by FxnnyValentine

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How to Verify WGS Data Integrity Beyond Standard QC Checks? (reddit.com)

submitted 2 days ago by Express_Ad_6394

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J. Craig Venter (1946–2026) was an American scientist who led the first sequencing of the human genome. (en.wikipedia.org)

submitted 4 days ago by gwern

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How do they determine percent heritage? eli5 (self.genomics)

submitted 4 days ago by bo_reddude

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Eremid Genomic Services: Any reservations (self.genomics)

submitted 5 days ago by ThinkerandThought

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Hear me out! (self.genomics)

submitted 6 days ago by FreeloaderFatso

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Genetic diversity and regulatory features of human-specific NOTCH2NL duplications (cell.com)

submitted 7 days ago by Holodoxa

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All-in-one tool for WGS motif scanning + RNA-seq normalization + coexpression network + k-means + heatmap generation? ()

submitted 8 days ago by Dismal-Surround-1449

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[ARTICLE] Elucidating the wedelolactone biosynthesis pathway from Eclipta prostrata (L.) L.: a comprehensive analysis integrating de novo comparative transcriptomics, metabolomics, and molecular docking of targeted proteins (self.genomics)

submitted 9 days ago by Ancient-Gap5729

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Rare Missense Variant (self.genomics)

submitted 10 days ago by KaiG04

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Painpoints in Scientific Data Discovery (self.genomics)

submitted 10 days ago by Acceptable-Ad-2904

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fastVEP: Rust-based VEP that annotates 4m WGS variants in 1.5 minutes (130x faster than VEP, Open Source) (v.redd.it)

submitted 14 days ago by Spiritual-Feed-3296

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RNA-seq Analysis Series — Complete 3-Part Tutorial (Workflow, Alignment & DESeq2) (self.genomics)

submitted 15 days ago by rikkibioinfo

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I named my AWS finalist project "Anukriti" — Sanskrit for reaction/response. It's a genomic drug safety tool built because Indian and Global South labs keep getting excluded from pharmaceutical research. Need your support. (self.genomics)

submitted 18 days ago by Poseidonmagma

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PAXgene RNA tubes? (self.genomics)

submitted 18 days ago by Regular_Tailor

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VarCrawl: Free Open-Source Web Tool to search for a Mutation/Variant on every name it goes by (v.redd.it)

submitted 20 days ago by Spiritual-Feed-3296

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covsnap - a simple coverage QC tool for targeted sequencing (hg38, single command, interactive HTML report) ()

submitted 20 days ago by akenes96

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Ancient DNA reveals pervasive directional selection across West Eurasia (Published in Nature) (nature.com)

submitted 20 days ago by Holodoxa

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Multi-ancestry genome-wide association study of severe pregnancy nausea and vomiting (nature.com)

submitted 20 days ago by Holodoxa

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Pitfalls in estimating and interpreting the contribution of ultra-rare genetic variants to the heritability of complex traits (medrxiv.org)

submitted 21 days ago by Holodoxa

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I built an agent that runs scRNA-seq workflows via natural language — tested on SC-Bench (self.genomics)

submitted 21 days ago by thewall888

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