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dsl2 port #182
dsl2 port #182
Commits on Nov 18, 2020
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Commits on Nov 19, 2020
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Brackets shouldn't make any difference
This code works for ch_multiqc_custom_config - why not here?
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Commits on Dec 3, 2020
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Commits on Jan 19, 2021
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check in required nf-core modules
* fastqc * picard/markduplicates * preseq/lcextrap * samtools/flagstat * samtools/index * samtools/stats * samtools/sort * trimgalore * multiqc
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* bismark/genome_preparation * bismark/align * bismark/deduplicate * bismark/extract * bismark/report * bismark/summary TODO: write tests and add to nf-core/modules
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* bwameth/align * bwameth/index TODO: write tests and add to nf-core/modules
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add required methyldackel modules
* methyldackel/extract * methyldackel/mbias TODO: write tests and add to nf-core modules
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add required qualimap/bamqc module
TODO: write tests and add to nf-core/modules
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add required samtools/faidx module
TODO: write tests and add to nf-core/modules
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this is inspired by the functionality in nf-core/nanoseq and nf-core/rnaseq The idea is to require a samplesheet to run the pipeline, which will allow for single/paired end auto-detection and mapping samples against different reference genomes. addresses nf-core#181
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update test.config to use samplesheet
TODO: needs change in nf-core/test-datasets
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Commits on Feb 11, 2021
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Merge pull request nf-core#179 from ewels/known_splices-collect-ifEmpty
Template update + fix skipped alignment
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Commits on Feb 12, 2021
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Commits on Feb 15, 2021
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Commits on Feb 19, 2021
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Commits on Feb 20, 2021
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Commits on Feb 21, 2021
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Merge pull request nf-core#185 from ewels/software-update
Tidy up lint warnings
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Commits on Mar 18, 2021
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Commits on Mar 19, 2021
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Commits on Mar 22, 2021
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check in required nf-core modules
* fastqc * picard/markduplicates * preseq/lcextrap * samtools/flagstat * samtools/index * samtools/stats * samtools/sort * trimgalore * multiqc
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* bismark/genome_preparation * bismark/align * bismark/deduplicate * bismark/extract * bismark/report * bismark/summary TODO: write tests and add to nf-core/modules
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* bwameth/align * bwameth/index TODO: write tests and add to nf-core/modules
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add required methyldackel modules
* methyldackel/extract * methyldackel/mbias TODO: write tests and add to nf-core modules
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add required qualimap/bamqc module
TODO: write tests and add to nf-core/modules
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add required samtools/faidx module
TODO: write tests and add to nf-core/modules
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this is inspired by the functionality in nf-core/nanoseq and nf-core/rnaseq The idea is to require a samplesheet to run the pipeline, which will allow for single/paired end auto-detection and mapping samples against different reference genomes. addresses nf-core#181
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update test.config to use samplesheet
TODO: needs change in nf-core/test-datasets
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Commits on Mar 23, 2021
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Commits on Mar 24, 2021
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