File: snpsplit.md

package info (click to toggle)
multiqc 1.21%2Bdfsg-3
  • links: PTS, VCS
  • area: main
  • in suites: forky, sid
  • size: 30,164 kB
  • sloc: python: 52,323; javascript: 7,064; sh: 76; makefile: 21
file content (12 lines) | stat: -rw-r--r-- 904 bytes parent folder | download | duplicates (2)
1
2
3
4
5
6
7
8
9
10
11
12
---
name: SNPsplit
url: https://www.bioinformatics.babraham.ac.uk/projects/SNPsplit/
description: SNPsplit is an allele-specific alignment sorter, which is designed to read in alignment files in SAM/BAM format and determine the allelic origin of reads that cover known SNP positions.
---

Currently only the "Allele-tagging" and "Allele-sorting" reports are supported.
The log files from the genome creation steps are not parsed and there are no plots/tables produced from the "SNP coverage" report.

Differences between the numbers in the tagging and sorting reports are due to paired-end reads.
For these, if only a single mate in a pair is assigned to a genome then it will "rescue" its mate and both will be "sorted" into that genome (even though only one of them was tagged).
Conversely, if the mates in a pair are tagged as arising from different genomes, then the pair as a whole is unassignable.