3 posts
A practical map of the software that turns raw multi-omics files into results you can query, with the commands, formats, and failure modes that matter for a single person's data.
Cloning tools like SnapGene and Geneious answer a different question than personal genome analysis. A concrete stack for going from FASTQ to annotated variants, with the tools, flags, file formats, and failure modes that matter.
A concrete stack for working with personal genome, transcriptome, proteome, and biomarker data: file formats, tools, commands, and where each approach breaks down.