Published May 1, 2019
| Version 0
Software
Open
Analysis scripts for: Insights about variation in meiosis from 31,228 human sperm genomes
Creators
- 1. Department of Genetics, Harvard Medical School; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard
Description
This repository holds scripts that call crossovers, determine ploidy, and perform various other analyses for data generated via Sperm-seq. The methods from the preprint/paper ("Insights about variation in meiosis from 31,228 human sperm genomes") explain the purpose of many of the scripts, and the PDF file included in this repository (_scriptdocumentation_spermseq.pdf) provides more detailed script documentation and instructions for using these scripts. Data generated with these methods are available in the companion repository (DOI: 10.5281/zenodo.2581571).
Files
_scriptdocumentation_spermseq.pdf
Files
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Additional details
Related works
- Is supplement to
- https://www.biorxiv.org/content/10.1101/625202v1 (URL)
- References
- 10.5281/zenodo.2581571 (DOI)