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[DRAFT] Add telseq "a software that estimates telomere length " #1665

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1 change: 1 addition & 0 deletions CHANGELOG.md
Original file line number Diff line number Diff line change
Expand Up @@ -11,6 +11,7 @@ and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0

- [1640](https://github.com/nf-core/sarek/pull/1620) - Add `lofreq` as a tumor-only variant caller.
- [1642](https://github.com/nf-core/sarek/pull/1642) - Back to dev
- Added Telseq

### Changed

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28 changes: 28 additions & 0 deletions conf/modules/telseq.config
Original file line number Diff line number Diff line change
@@ -0,0 +1,28 @@
/*
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
Config file for defining DSL2 per module options and publishing paths
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
Available keys to override module options:
ext.args = Additional arguments appended to command in module.
ext.args2 = Second set of arguments appended to command in module (multi-tool modules).
ext.args3 = Third set of arguments appended to command in module (multi-tool modules).
ext.prefix = File name prefix for output files.
ext.when = When to run the module.
----------------------------------------------------------------------------------------
*/

// TELSEQ

process {
if (params.tools && params.tools.split(',').contains('telseq')) {

withName: 'TELSEQ' {
ext.when = { params.tools && params.tools.split(',').contains('telseq') }
publishDir = [
mode: params.publish_dir_mode,
path: { "${params.outdir}/telseq/" },
pattern: "*.tsv"
]
}
}
}
18 changes: 18 additions & 0 deletions docs/output.md
Original file line number Diff line number Diff line change
Expand Up @@ -43,6 +43,8 @@ The pipeline is built using [Nextflow](https://www.nextflow.io/) and processes d
- [Sentieon Haplotyper joint germline variant calling](#sentieon-haplotyper-joint-germline-variant-calling)
- [Lofreq](#lofreq)
- [Strelka](#strelka)
- Telomeres
- [Telseq](#telseq)
- [Structural Variants](#structural-variants)
- [Manta](#manta)
- [TIDDIT](#tiddit)
Expand Down Expand Up @@ -585,6 +587,22 @@ For further downstream analysis, take a look [here](https://github.com/Illumina/

</details>

### Telomeres

#### Telseq

[Telseq](https://github.com/zd1/telseq) is a software that estimates telomere length from whole genome sequencing data.

<details markdown = "1">
<summary>Output files</summary>

**Output directory: `{outdir}/telseq/`**

-`<sample>.telseq.tsv`
- Telseq output
</details>


### Structural Variants

#### Manta
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1 change: 1 addition & 0 deletions docs/usage.md
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Expand Up @@ -585,6 +585,7 @@ This list is by no means exhaustive and it will depend on the specific analysis
| [mpileup](https://www.htslib.org/doc/samtools-mpileup.html) | x | x | x | x | x | - |
| [Strelka](https://github.com/Illumina/strelka) | x | x | x | x | x | x |
| [Manta](https://github.com/Illumina/manta) | x | x | x | x | x | x |
| [Telseq](https://github.com/zd1/telseq) | x | x | x | x | x | x |
| [TIDDIT](https://github.com/SciLifeLab/TIDDIT) | x | x | x | x | x | x |
| [ASCAT](https://github.com/VanLoo-lab/ascat) | x | x | - | - | - | x |
| [CNVKit](https://cnvkit.readthedocs.io/en/stable/) | x | x | - | x | x | x |
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