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[automated] Fix code linting
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nf-core-bot committed Aug 6, 2024
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4 changes: 2 additions & 2 deletions README.md
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Expand Up @@ -54,7 +54,7 @@ Depending on the options and samples provided, the pipeline can currently perfor
- `freebayes`
- `GATK HaplotypeCaller`
- `Manta`
- IndexCov
- IndexCov
- `mpileup`
- `MSIsensor-pro`
- `Mutect2`
Expand Down Expand Up @@ -170,7 +170,7 @@ We thank the following people for their extensive assistance in the development
- [pallolason](https://github.com/pallolason)
- [Paul Cantalupo](https://github.com/pcantalupo)
- [Phil Ewels](https://github.com/ewels)
- [Pierre Lindenbaum][https://github.com/lindenb=
- [Pierre Lindenbaum]https://github.com/lindenb=
- [Sabrina Krakau](https://github.com/skrakau)
- [Sam Minot](https://github.com/sminot)
- [Sebastian-D](https://github.com/Sebastian-D)
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32 changes: 15 additions & 17 deletions docs/output.md
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Expand Up @@ -581,23 +581,21 @@ The output is scaled to around 1. So a long stretch with values of 1.5 would be

**Output directory: `{outdir}/variantcalling/indexcov/`**

In addition to the interactive HTML files, `indexcov` outputs a number of text files:

+ `$prefix-indexcov.ped`: a .ped/.fam file with the inferred sex in the appropriate column if the sex chromosomes were found.
the CNX and CNY columns indicating the floating-point estimate of copy-number for those chromosomes.
`bins.out`: how many bins had a coverage value outside of (0.85, 1.15). high values can indicate high-bias samples.
`bins.lo`: number of bins with value < 0.15. high values indicate missing data.
`bins.hi`: number of bins with value > 1.15.
`bins.in`: number of bins with value inside of (0.85, 1.15)
`p.out`: `bins.out/bins.in`
`PC1...PC5`: PCA projections calculated with depth of autosomes.

+ `$prefix-indexcov.roc`: tab-delimited columns of chrom, scaled coverage cutoff, and $n_samples columns where each indicates the
proportion of 16KB blocks at or above that scaled coverage value.
+ `$prefix-indexcov.bed.gz`: a bed file with columns of chrom, start, end, and a column per sample where the values indicate there
scaled coverage for that sample in that 16KB chunk.


In addition to the interactive HTML files, `indexcov` outputs a number of text files:

- `$prefix-indexcov.ped`: a .ped/.fam file with the inferred sex in the appropriate column if the sex chromosomes were found.
the CNX and CNY columns indicating the floating-point estimate of copy-number for those chromosomes.
`bins.out`: how many bins had a coverage value outside of (0.85, 1.15). high values can indicate high-bias samples.
`bins.lo`: number of bins with value < 0.15. high values indicate missing data.
`bins.hi`: number of bins with value > 1.15.
`bins.in`: number of bins with value inside of (0.85, 1.15)
`p.out`: `bins.out/bins.in`
`PC1...PC5`: PCA projections calculated with depth of autosomes.

- `$prefix-indexcov.roc`: tab-delimited columns of chrom, scaled coverage cutoff, and $n_samples columns where each indicates the
proportion of 16KB blocks at or above that scaled coverage value.
- `$prefix-indexcov.bed.gz`: a bed file with columns of chrom, start, end, and a column per sample where the values indicate there
scaled coverage for that sample in that 16KB chunk.

#### Manta

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