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Remove sample specific options and use them as rule specific.

Merged BIOPZ-Katsantoni Maria requested to merge restructure_sample_table into dev
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@@ -122,12 +122,24 @@ map_genome_star:
--outFilterMultimapScoreRange: '0'
# keep only those reads that contain junctions that passed filtering into SJ.out.tab. (default 'Normal', ZARP recommends 'BySJout', as this reduces the number of ”spurious” junctions )
--outFilterType: 'BySJout'
# type of read ends alignment: force end-to-end read alignment, do not soft-clip
--alignEndsType: 'EndToEnd'
# extract junctions, insert them into the genome index and re-map reads in a 2nd mapping pass
--twopassMode: Basic
# alignments (all of them) will be output only if the read maps to no more loci than 10
--outFilterMultimapNmax: '10'
pe_map_genome_star:
# the score range below the maximum score for multimapping alignments (default 1, ZARP recommends 0)
--outFilterMultimapScoreRange: '0'
# keep only those reads that contain junctions that passed filtering into SJ.out.tab. (default 'Normal', ZARP recommends 'BySJout', as this reduces the number of ”spurious” junctions )
--outFilterType: 'BySJout'
# type of read ends alignment: force end-to-end read alignment, do not soft-clip
--alignEndsType: 'EndToEnd'
# extract junctions, insert them into the genome index and re-map reads in a 2nd mapping pass
--twopassMode: Basic
# alignments (all of them) will be output only if the read maps to no more loci than 10
--outFilterMultimapNmax: '10'
quantification_salmon:
# correct for sequence specific biases](https://salmon.readthedocs.io/en/latest/salmon.html#seqbias
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