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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-variant-calling

Dispatch WGS, WES, or targeted DNA variant requests to germline, somatic, or UMI-panel skills, then plan public nf-core/sarek, GATK4, DeepVariant, samtools, or bcftools workflows.

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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