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Slight tweaks to help mssage
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main.nf

Lines changed: 3 additions & 3 deletions
Original file line numberDiff line numberDiff line change
@@ -32,14 +32,14 @@ def helpMessage() {
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--singleEnd Specifies that the input is single end reads (required if not pairedEnd)
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--pairedEnd Specifies that the input is paired end reads (required if not singleEnd)
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--bam Specifies that the input is in BAM format
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--fasta Path to Fasta reference (required if not iGenome reference)
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--fasta Path and name of FASTA reference file (required if not iGenome reference). File suffixes can be: '.fa', '.fn', '.fna', '.fasta'
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--genome Name of iGenomes reference (required if not fasta reference)
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Input Data Additional Options:
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--snpcapture Runs in SNPCapture mode (specify a BED file if you do this!)
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References If not specified in the configuration file, or you wish to overwrite any of the references.
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--bwa_index Prefix of the BWA index files including the full path (everything before the endings '.amb' '.ann' '.bwt' most likely the same value supplied with the --fasta option)
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--bwa_index Path and name of a a bwa indexed FASTA reference file with index suffixes (i.e. everything before the endings '.amb' '.ann' '.bwt'. Most likely the same value supplied with the --fasta option)
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--bedfile Path to BED file for SNPCapture methods
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--seq_dict Path to picard sequence dictionary file (typically ending in '.dict')
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--fasta_index Path to samtools FASTA index (typically ending in '.fai')
@@ -54,7 +54,7 @@ def helpMessage() {
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--skip_deduplication
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Complexity Filtering
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--complexity_filter_poly_g Run poly-G removal on FASTQ files
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--complexity_filter_poly_g Run poly-G removal on FASTQ files
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--complexity_filter_poly_g_min Specify length of poly-g min for clipping to be performed (default: 10)
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Clipping / Merging

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