Documentation of best practices, coding tips, and ongoing projects developed by the Pugh Lab
- Cancer genome variant:
- copy-number
- fusion
- SNP
- SNV
- structural-variant
- mutation-signature
- Topics:
- immunogenomics
- Bulk RNA-seq
- single-cell
- cell-free-dna
- epigenetics
- methylation
- minimal-residual-disease
- Type:
- wrapper
- pipeline
- tool
- package
- docker
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General guideline:
- ALWAYS comment your code
- Document all functions!!
- Add README document when there’s other people who will be using your tool
- For R, use documentation within code and easily port to markdown with Roxygen: http://r-pkgs.had.co.nz/man.html
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Google Python style guide:
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Google R style guide: