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fix: STAR mtx conversion when using GeneFull #135
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When STAR is run with the flag `--soloFeatures GeneFull` (permits counting of exonic and intronic reads), the output is stored in `*.Solo.out/GeneFull/` and not `*.Solo.out/Gene`. As a result, matrix conversion results in an error, as matrix, barcodes and features cannot be found. This error can be fixed by adding an asterisk in the file path provided to the mtx conversion modules.
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Gzipping outputs for file compression and downstream compatibility with scflow (which requires zipped format, as outputted by cellranger).
fmalmeida
approved these changes
Jul 30, 2022
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Looks good to me 😄
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When STAR is run with the flag
--soloFeatures GeneFull
(permitscounting of exonic and intronic reads), the output is stored in
*.Solo.out/GeneFull/
and not*.Solo.out/Gene
. As a result, matrixconversion results in an error, as matrix, barcodes and features cannot
be found. This error can be fixed by adding an asterisk in the file
path provided to the mtx conversion modules.
Additionally added compression of starsolo outputs, both for storage
purposes and for downstream compatibility with nf-core/scflow (which
requires gzipped outputs similar to cellranger).
PR checklist
nf-core lint
).nextflow run . -profile test,docker --outdir <OUTDIR>
).CHANGELOG.md
is updated.