
1/ Sex chromosomes are bias magnets in WGS. Early large-scale genomes often showed weird copy-number or coverage patterns on X and Y that looked like biology, but were really mapping artifacts. https://t.co/YnApmtxHqm

1/ RNA‑seq batch effects are one of the easiest ways to fool yourself in genomics. They can create beautiful, completely wrong biology if you’re not careful. https://t.co/VBtySwZHVL

Single-cell integration and multi-modal profiling reveals phenotypes and spatial organization of neutrophils in colorectal cancer https://t.co/0FLusa7vuB https://t.co/8MswWoLhCa

Multiomic integration reveals tumoral heterogeneity of lipid dependence within lethal group 3 medulloblastoma https://t.co/tpjJiRa08t https://t.co/z7aIYerTqO

Why are there intronic reads in your bulk RNA-seq data? You're not alone—it's common, and the reasons are more layered than you think. Let’s break it down. 🧵 https://t.co/SNJnohqHUM

🧵 That V-plot showing transcription factor binding? It might be an artifact. New research shows chromatin fragmentation methods create patterns even on naked DNA. Here's what went wrong. https://t.co/79B5c0ulgD

1/ Claude Code just hallucinated ENSEMBL IDs for my volcano plot. (it happened last week for real) I asked it to highlight specific genes. The data matrix uses ENSEMBL identifiers. Instead of flagging that it couldn't map the gene symbols, it invented...

🧵 10 free bioinformatics tools you should know in 2026. These will save you time, money, and headaches. https://t.co/t8amdLE4MX

Recruitment of BRD4 to the ASXL1 genomic targets depends on the extra-terminal domain of BRD4 https://t.co/sRbcAAMqPx https://t.co/IbD0EM56SS

🧵 Need gene lengths for every mouse gene? Bioconductor annotation packages make this simple. Here's how to get gene lengths using TxDb.Mmusculus and https://t.co/FiqDAsSPa0.db. https://t.co/VyE36hp3om