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pleasefixai/ngs-analysis

v1.0.1MIT

Guides for sequencing analyses: FASTQ QC, RNA-seq, variants, single-cell and microbiome.

ngs-dna-somatic-variants

Run or plan tumor-normal, tumor-only, WGS, WES, or cancer-panel somatic variant workflows with pairing, contamination, panel-of-normals, purity, QC, and annotation checks.

Read SKILL.md at the source

Pinned to revision 4e8964e24a5a, so it is the text this page describes rather than whatever the author pushed since.

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