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2 changes: 1 addition & 1 deletion .github/workflows/ci.yml
Original file line number Diff line number Diff line change
Expand Up @@ -119,7 +119,7 @@ jobs:
nextflow run ${GITHUB_WORKSPACE} -profile test,docker --mapper 'circularmapper' --circulartarget 'NC_007596.2'
- name: MAPPER_BWAMEM Test running with BWA Mem
run: |
nextflow run ${GITHUB_WORKSPACE} -profile test,docker --mapper 'bwamem'
nextflow run ${GITHUB_WORKSPACE} -profile test,docker --mapper 'bwamem' --skip_collapse
- name: MAPPER_BT2 Test running with BowTie2
run: |
nextflow run ${GITHUB_WORKSPACE} -profile test,docker --mapper 'bowtie2' --bt2_alignmode 'local' --bt2_sensitivity 'sensitive' --bt2n 1 --bt2l 16 --bt2_trim5 1 --bt2_trim3 1
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2 changes: 2 additions & 0 deletions CHANGELOG.md
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Expand Up @@ -18,6 +18,8 @@ and this project adheres to [Semantic Versioning](http://semver.org/spec/v2.0.0.
- [#851](https://github.com/nf-core/eager/issues/851) Fixes a file-name clash during additional_library_merge, post-BAM trimming of different UDG treated libraries of a sample
- Renamed a range of MultiQC general stats table headers to improve clarity, documentation has been updated accordingly
- [#857](https://github.com/nf-core/eager/issues/857) Corrected samtools fastq flag to _retain_ read-pair information when converting off-target BAM files to fastq in paired-end mapping (❤ to @alexhbnr for reporting)
- [#858](https://github.com/nf-core/eager/pull/858) Corrected tutorials to reflect updated BAM trimming flags (❤ to @marcel-keller for reporting)
- [#866](https://github.com/nf-core/eager/issues/866) Fixed a typo in the indexing step of BWA mem when not-collapsing (❤ to @alexhbnr for reporting)
- Corrected tutorials to reflect updated BAM trimming flags (❤ to @marcel-keller for reporting and correcting)

### `Dependencies`
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4 changes: 2 additions & 2 deletions environment.yml
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Expand Up @@ -26,12 +26,12 @@ dependencies:
- bioconda::qualimap=2.2.2d
- bioconda::vcf2genome=0.91
- bioconda::damageprofiler=0.4.9 # Don't upgrade - later versions don't allow java 8
- bioconda::multiqc=1.11
- bioconda::multiqc=1.12
- bioconda::pmdtools=0.60
- bioconda::bedtools=2.30.0
- conda-forge::libiconv=1.16
- conda-forge::pigz=2.6
- bioconda::sequencetools=1.4.0.6
- bioconda::sequencetools=1.5.2
- bioconda::preseq=3.1.2
- bioconda::fastp=0.20.1
- bioconda::bamutil=1.0.15
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2 changes: 1 addition & 1 deletion main.nf
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Expand Up @@ -1318,7 +1318,7 @@ process bwamem {
if (!params.single_end && params.skip_collapse){
"""
bwa mem -t ${split_cpus} $fasta $r1 $r2 -R "@RG\\tID:ILLUMINA-${libraryid}\\tSM:${samplename}\\tPL:illumina\\tPU:ILLUMINA-${libraryid}-${seqtype}" | samtools sort -@ ${split_cpus} -O bam - > "${libraryid}"_"${seqtype}".mapped.bam
samtools index ${size} -@ ${task.cpus} "${libraryid}".mapped.bam
samtools index ${size} -@ ${task.cpus} "${libraryid}"_"${seqtype}".mapped.bam
"""
} else {
"""
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