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Merge branch 'dev' into metaphlan3/mergemetaphlantables

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James A. Fellows Yates 2022-09-15 13:08:57 +02:00 committed by GitHub
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12 changed files with 203 additions and 55 deletions

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@ -12,6 +12,8 @@
## Introduction
> ⚠️ This pipeline is still under development! While the pipeline is usable, not all functionality will be available!
<!-- TODO nf-core: Write a 1-2 sentence summary of what data the pipeline is for and what it does -->
**nf-core/taxprofiler** is a bioinformatics best-practice analysis pipeline for taxonomic profiling of shotgun metagenomic data. It allows for in-parallel profiling with multiple profiling tools against multiple databases, produces standardised output tables.

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@ -294,6 +294,15 @@ process {
]
}
withName: KRAKENTOOLS_COMBINEKREPORTS {
ext.prefix = { "kraken2_${meta.id}_combined_reports" }
publishDir = [
path: { "${params.outdir}/kraken2/" },
mode: params.publish_dir_mode,
pattern: '*.{txt}'
]
}
withName: KRONA_CLEANUP {
ext.prefix = params.perform_runmerging ? { "${meta.id}-${meta.db_name}" } : { "${meta.id}-${meta.run_accession}-${meta.db_name}" }
publishDir = [
@ -367,6 +376,15 @@ process {
]
}
withName: KRAKENTOOLS_COMBINEKREPORTS_CENTRIFUGE {
ext.prefix = { "centrifuge_${meta.id}_combined_reports" }
publishDir = [
path: { "${params.outdir}/centrifuge/" },
mode: params.publish_dir_mode,
pattern: '*.{txt}'
]
}
withName: KAIJU_KAIJU {
ext.prefix = params.perform_runmerging ? { "${meta.id}-${meta.db_name}" } : { "${meta.id}-${meta.run_accession}-${meta.db_name}" }
publishDir = [
@ -378,7 +396,7 @@ process {
}
withName: KAIJU_KAIJU2TABLE {
ext.prefix = { "${meta.id}_combined_reports" }
ext.prefix = { "kaiju_${meta.id}_combined_reports" }
publishDir = [
path: { "${params.outdir}/kaiju/" },
mode: params.publish_dir_mode,

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@ -410,3 +410,13 @@ We recommend adding the following line to your environment to limit this (typica
```bash
NXF_OPTS='-Xms1g -Xmx4g'
```
## Troubleshooting and FAQs
### I get a warning during centrifuge_kreport process with exit status 255.
When a sample has insufficient hits for abundance estimation, the resulting `report.txt` file will be empty.
When trying to convert this to a kraken-style report, the conversion tool will exit with a status code `255`, and provide a `WARN`.
This is **not** an error nor a failure of the pipeline, just your sample has no hits to the provided database when using centrifuge.

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@ -43,8 +43,7 @@
},
"fastp": {
"branch": "master",
"git_sha": "7e8ad566883449e7939062b5e2bcf53fc1e0002f",
"patch": "modules/nf-core/modules/fastp/fastp.diff"
"git_sha": "2c70c1c1951aaf884d2e8d8d9c871db79f7b35aa"
},
"fastqc": {
"branch": "master",
@ -74,6 +73,10 @@
"branch": "master",
"git_sha": "409a308ba46284d8ebb48c2c1befd6f6433db3f7"
},
"krakentools/combinekreports": {
"branch": "master",
"git_sha": "ee0346b4d14ffdc15ce7e093ca1363cd07c9bd78"
},
"krakentools/kreport2krona": {
"branch": "master",
"git_sha": "233fa70811a03a4cecb2ece483b5c8396e2cee1d"
@ -140,7 +143,7 @@
},
"untar": {
"branch": "master",
"git_sha": "5e7b1ef9a5a2d9258635bcbf70fcf37dacd1b247"
"git_sha": "393dbd6ddafe3f18eac02893dd4a21e4d45de679"
}
}
}

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@ -1,33 +0,0 @@
Changes in module 'nf-core/modules/fastp'
--- modules/nf-core/modules/fastp/main.nf
+++ modules/nf-core/modules/fastp/main.nf
@@ -33,9 +33,8 @@
def fail_fastq = save_trimmed_fail ? "--failed_out ${prefix}.fail.fastq.gz" : ''
"""
[ ! -f ${prefix}.fastq.gz ] && ln -sf $reads ${prefix}.fastq.gz
- cat ${prefix}.fastq.gz \\
- | fastp \\
- --stdin \\
+
+ fastp \\
--stdout \\
--in1 ${prefix}.fastq.gz \\
--thread $task.cpus \\
@@ -45,6 +44,7 @@
$args \\
2> ${prefix}.fastp.log \\
| gzip -c > ${prefix}.fastp.fastq.gz
+
cat <<-END_VERSIONS > versions.yml
"${task.process}":
fastp: \$(fastp --version 2>&1 | sed -e "s/fastp //g")
@@ -69,6 +69,7 @@
--detect_adapter_for_pe \\
$args \\
2> ${prefix}.fastp.log
+
cat <<-END_VERSIONS > versions.yml
"${task.process}":
************************************************************

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@ -26,11 +26,11 @@ process FASTP {
script:
def args = task.ext.args ?: ''
// Added soft-links to original fastqs for consistent naming in MultiQC
def prefix = task.ext.prefix ?: "${meta.id}"
def fail_fastq = save_trimmed_fail && meta.single_end ? "--failed_out ${prefix}.fail.fastq.gz" : save_trimmed_fail && !meta.single_end ? "--unpaired1 ${prefix}_1.fail.fastq.gz --unpaired2 ${prefix}_2.fail.fastq.gz" : ''
// Added soft-links to original fastqs for consistent naming in MultiQC
// Use single ended for interleaved. Add --interleaved_in in config.
if (meta.single_end) {
def fail_fastq = save_trimmed_fail ? "--failed_out ${prefix}.fail.fastq.gz" : ''
if ( task.ext.args?.contains('--interleaved_in') ) {
"""
[ ! -f ${prefix}.fastq.gz ] && ln -sf $reads ${prefix}.fastq.gz
@ -45,13 +45,32 @@ process FASTP {
2> ${prefix}.fastp.log \\
| gzip -c > ${prefix}.fastp.fastq.gz
cat <<-END_VERSIONS > versions.yml
"${task.process}":
fastp: \$(fastp --version 2>&1 | sed -e "s/fastp //g")
END_VERSIONS
"""
} else if (meta.single_end) {
"""
[ ! -f ${prefix}.fastq.gz ] && ln -sf $reads ${prefix}.fastq.gz
fastp \\
--stdout \\
--in1 ${prefix}.fastq.gz \\
--out1 ${prefix}.fastp.fastq.gz \\
--thread $task.cpus \\
--json ${prefix}.fastp.json \\
--html ${prefix}.fastp.html \\
$fail_fastq \\
$args \\
2> ${prefix}.fastp.log
cat <<-END_VERSIONS > versions.yml
"${task.process}":
fastp: \$(fastp --version 2>&1 | sed -e "s/fastp //g")
END_VERSIONS
"""
} else {
def fail_fastq = save_trimmed_fail ? "--unpaired1 ${prefix}_1.fail.fastq.gz --unpaired2 ${prefix}_2.fail.fastq.gz" : ''
def merge_fastq = save_merged ? "-m --merged_out ${prefix}.merged.fastq.gz" : ''
"""
[ ! -f ${prefix}_1.fastq.gz ] && ln -sf ${reads[0]} ${prefix}_1.fastq.gz
@ -70,7 +89,6 @@ process FASTP {
$args \\
2> ${prefix}.fastp.log
cat <<-END_VERSIONS > versions.yml
"${task.process}":
fastp: \$(fastp --version 2>&1 | sed -e "s/fastp //g")

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@ -21,7 +21,8 @@ input:
type: file
description: |
List of input FastQ files of size 1 and 2 for single-end and paired-end data,
respectively.
respectively. If you wish to run interleaved paired-end data, supply as single-end data
but with `--interleaved_in` in your `modules.conf`'s `ext.args` for the module.
- save_trimmed_fail:
type: boolean
description: Specify true to save files that failed to pass trimming thresholds ending in `*.fail.fastq.gz`

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@ -0,0 +1,34 @@
process KRAKENTOOLS_COMBINEKREPORTS {
label 'process_low'
conda (params.enable_conda ? "bioconda::krakentools=1.2" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/krakentools:1.2--pyh5e36f6f_0':
'quay.io/biocontainers/krakentools:1.2--pyh5e36f6f_0' }"
input:
tuple val(meta), path(kreports)
output:
tuple val(meta), path("*.txt"), emit: txt
path "versions.yml", emit: versions
when:
task.ext.when == null || task.ext.when
script:
def args = task.ext.args ?: ''
prefix = task.ext.prefix ?: "${meta.id}"
def VERSION = '1.2' // WARN: Version information not provided by tool on CLI. Please update this string when bumping container versions.
"""
combine_kreports.py \\
-r ${kreports} \\
-o ${prefix}.txt \\
${args}
cat <<-END_VERSIONS > versions.yml
"${task.process}":
combine_kreports.py: ${VERSION}
END_VERSIONS
"""
}

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@ -0,0 +1,43 @@
name: krakentools_combinekreports
description: Takes a Kraken report file and prints out a krona-compatible TEXT file
keywords:
- kraken
- krakentools
- metagenomics
- table
- combining
- merging
tools:
- krakentools:
description: KrakenTools is a suite of scripts to be used for post-analysis of Kraken/KrakenUniq/Kraken2/Bracken results. Please cite the relevant paper if using KrakenTools with any of the listed programs.
homepage: https://github.com/jenniferlu717/KrakenTools
licence: ["GPL v3"]
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- kreports:
type: file
description: List of kraken-style report files
pattern: "*.{txt,kreport}"
output:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- versions:
type: file
description: File containing software versions
pattern: "versions.yml"
- txt:
type: file
description: Combined kreport file of all input files
pattern: "*.txt"
authors:
- "@jfy133"

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@ -25,12 +25,23 @@ process UNTAR {
"""
mkdir output
## Ensures --strip-components only applied when top level of tar contents is a directory
## If just files or multiple directories, place all in output
if [[ \$(tar -tzf ${archive} | grep "/\$" | wc -l) -eq 1 ]]; then
tar \\
-C output --strip-components 1 \\
-xzvf \\
$args \\
$archive \\
$args2
else
tar \\
-C output \\
-xzvf \\
$args \\
$archive \\
$args2
fi
mv output ${untar}

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@ -26,9 +26,9 @@ output:
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- untar:
type: file
description:
pattern: "*.*"
type: directory
description: Directory containing contents of archive
pattern: "*/"
- versions:
type: file
description: File containing software versions
@ -36,3 +36,5 @@ output:
authors:
- "@joseespinosa"
- "@drpatelh"
- "@matthdsm"
- "@jfy133"

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@ -3,8 +3,10 @@
//
include { KAIJU_KAIJU2TABLE } from '../../modules/nf-core/modules/kaiju/kaiju2table/main'
include { MOTUS_MERGE } from '../../modules/nf-core/modules/motus/merge/main'
include { KRAKENTOOLS_COMBINEKREPORTS } from '../../modules/nf-core/modules/krakentools/combinekreports/main'
include { KRAKENTOOLS_COMBINEKREPORTS as KRAKENTOOLS_COMBINEKREPORTS_CENTRIFUGE } from '../../modules/nf-core/modules/krakentools/combinekreports/main'
include { METAPHLAN3_MERGEMETAPHLANTABLES } from '../../modules/nf-core/modules/metaphlan3/mergemetaphlantables/main'
include { MOTUS_MERGE } from '../../modules/nf-core/modules/motus/merge/main'
workflow STANDARDISATION_PROFILES {
take:
@ -24,6 +26,8 @@ workflow STANDARDISATION_PROFILES {
ch_input_profiles = profiles
.branch {
motus: it[0]['tool'] == 'motus'
kraken2: it[0]['tool'] == 'kraken2'
centrifuge: it[0]['tool'] == 'centrifuge'
metaphlan3: it[0]['tool'] == 'metaphlan3'
unknown: true
}
@ -45,6 +49,23 @@ workflow STANDARDISATION_PROFILES {
Standardise and aggregate
*/
// CENTRIFUGE
// Collect and replace id for db_name for prefix
// Have to sort by size to ensure first file actually has hits otherwise
// the script fails
ch_profiles_for_centrifuge = ch_input_profiles.centrifuge
.map { [it[0]['db_name'], it[1]] }
.groupTuple(sort: {-it.size()} )
.map {
[[id:it[0]], it[1]]
}
KRAKENTOOLS_COMBINEKREPORTS_CENTRIFUGE ( ch_profiles_for_centrifuge )
ch_standardised_tables = ch_standardised_tables.mix( KRAKENTOOLS_COMBINEKREPORTS_CENTRIFUGE.out.txt )
ch_multiqc_files = ch_multiqc_files.mix( KRAKENTOOLS_COMBINEKREPORTS_CENTRIFUGE.out.txt )
ch_versions = ch_versions.mix( KRAKENTOOLS_COMBINEKREPORTS_CENTRIFUGE.out.versions )
// Kaiju
// Collect and replace id for db_name for prefix
@ -60,7 +81,25 @@ workflow STANDARDISATION_PROFILES {
ch_multiqc_files = ch_multiqc_files.mix( KAIJU_KAIJU2TABLE.out.summary )
ch_versions = ch_versions.mix( KAIJU_KAIJU2TABLE.out.versions )
// Kraken2
// Collect and replace id for db_name for prefix
// Have to sort by size to ensure first file actually has hits otherwise
// the script fails
ch_profiles_for_kraken2 = ch_input_profiles.kraken2
.map { [it[0]['db_name'], it[1]] }
.groupTuple(sort: {-it.size()} )
.map {
[[id:it[0]], it[1]]
}
KRAKENTOOLS_COMBINEKREPORTS ( ch_profiles_for_kraken2 )
ch_standardised_tables = ch_standardised_tables.mix( KRAKENTOOLS_COMBINEKREPORTS.out.txt )
ch_multiqc_files = ch_multiqc_files.mix( KRAKENTOOLS_COMBINEKREPORTS.out.txt )
ch_versions = ch_versions.mix( KRAKENTOOLS_COMBINEKREPORTS.out.versions )
// MetaPhlAn3
ch_profiles_for_metaphlan3 = ch_input_profiles.metaphlan3
.map { [it[0]['db_name'], it[1]] }
.groupTuple()