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Read-based phasing of genomic variants, also called haplotype assembly
🐟 🍣 🍱 Highly-accurate & wicked fast transcript-level quantification from RNA-seq reads using selective alignment
Bioinformatics one liners from Ming Tang
R-package for structural equation modeling based on GWAS summary data
A reactive notebook for Python — run reproducible experiments, query with SQL, execute as a script, deploy as an app, and version with git. All in a modern, AI-native editor.
Common statistical tests are linear models (or: how to teach stats)
Small utilities to play with dbSNP rsID: annotate rsID for a var or get position for an rsID
Compute the neighborhood consolidation matrix and identify SHRs