CNVKIT_SEX(1)

πŸ“¦
version 0.9.13 Β· 3 versions
, in debian trixie, ubuntu noble, ubuntu questing, ubuntu resolute, ubuntu stonking

πŸ’– cnvkit_sex β€” the manual, but make it a vibe πŸ’–

okay so bestie, you found the CNVKIT_SEX(1) page (it lives in the User Commands section, very demure, very mindful) and honestly? it's a short one, so we're gonna get you fully caught up before your coffee even cools. πŸŽ€


✨ NAME ✨

cnvkit_sex β€” guess what sex your samples are, by peeking at the relative coverage of chromosomes X and Y. that's it. that's the whole job. πŸ‘‘


🌸 DESCRIPTION 🌸

so the way you actually run this is:

usage: cnvkit.py sex [-h] [-y] [-o FILENAME] filenames [filenames ...]

and here's the breakdown, babes. πŸ’…

🫢 positional arguments:

  • filenames β€” one or more files, bestie. these are your copy number or copy ratio files, and they come with the extensions *.cnn or *.cnr. that's the whole input situation. drop 'em in. 🌈

πŸ¦‹ options:

  • -h, --help β€” shows this help message and then dips. classic. πŸ’€
  • -y, --male-reference, --haploid-x-reference β€” okay this one's the plot twist. turn this on if you already know your inputs were normalized against a male reference. what that means: female samples will end up with +1 log-coverage of chrX. and if you don't do this, the flip side is that male samples would have -1 chrX. so like, pick your reference, know your reference, no cap. 🧚
  • -o FILENAME, --output FILENAME β€” names the output table file. give it a FILENAME, get a table. iconic. ✨
ngl bestie, that's genuinely the whole page. no sneaky extra flags hiding in here. i checked. twice. πŸ“

πŸ’œ a lil sign-off, because you deserve it πŸ’œ

this page is from cnvkit.py sex version 0.9.10, and it was dated July 2023 β€” so like, a lil vintage, still slaying. go forth and sex your samples (chromosomally. chromosomally!!! 😭). mwah. 🫢🌸⭐

πŸ“¦ where this page comes from