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Merge pull request #126 from MaxUlysse/FixLink
Fix typos
2 parents 1e30ff3 + 0d5fa6e commit d1a5691

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conf/igenomes.config

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@@ -53,14 +53,14 @@ params {
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bwa = "${params.igenomes_base}/Mus_musculus/Ensembl/GRCm38/Sequence/BWAIndex/genome.fa.{amb,ann,bwt,pac,sa}"
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chr_dir = "${params.igenomes_base}/Mus_musculus/Ensembl/GRCm38/Sequence/Chromosomes"
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chr_length = "${params.igenomes_base}/Mus_musculus/Ensembl/GRCm38/Sequence/Length/GRCm38.len"
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dbsnp = "${params.igenomes_base}/Mus_musculus/Ensembl/GRCm38/MouseGenomeProject/Annotation/mgp.v5.merged.snps_all.dbSNP142.vcf.gz"
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dbsnp_index = "${params.igenomes_base}/Mus_musculus/Ensembl/GRCm38/MouseGenomeProject/Annotation/mgp.v5.merged.snps_all.dbSNP142.vcf.gz.tbi"
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dbsnp = "${params.igenomes_base}/Mus_musculus/Ensembl/GRCm38/MouseGenomeProject/mgp.v5.merged.snps_all.dbSNP142.vcf.gz"
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dbsnp_index = "${params.igenomes_base}/Mus_musculus/Ensembl/GRCm38/MouseGenomeProject/mgp.v5.merged.snps_all.dbSNP142.vcf.gz.tbi"
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dict = "${params.igenomes_base}/Mus_musculus/Ensembl/GRCm38/Sequence/WholeGenomeFasta/genome.dict"
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fasta = "${params.igenomes_base}/Mus_musculus/Ensembl/GRCm38/Sequence/WholeGenomeFasta/genome.fa"
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fasta_fai = "${params.igenomes_base}/Mus_musculus/Ensembl/GRCm38/Sequence/WholeGenomeFasta/genome.fa.fai"
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intervals = "${params.igenomes_base}/Mus_musculus/Ensembl/GRCm38/Annotation/intervals/GRCm38_calling_list.bed"
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known_indels = "${params.igenomes_base}/Mus_musculus/Annotation/MouseGenomeProject/mgp.v5.merged.indels.dbSNP142.normed.vcf.gz"
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known_indels_index = "${params.igenomes_base}/Mus_musculus/Annotation/MouseGenomeProject/mgp.v5.merged.indels.dbSNP142.normed.vcf.gz.tbi"
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known_indels = "${params.igenomes_base}/Mus_musculus/Ensembl/GRCm38/MouseGenomeProject/mgp.v5.merged.indels.dbSNP142.normed.vcf.gz"
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known_indels_index = "${params.igenomes_base}/Mus_musculus/Ensembl/GRCm38/MouseGenomeProject/mgp.v5.merged.indels.dbSNP142.normed.vcf.gz.tbi"
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snpeff_db = 'GRCm38.86'
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species = 'mus_musculus'
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vep_cache_version = '98'

docs/input.md

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Input files for Sarek can be specified using a TSV file given to the `--input` command.
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The TSV file is a Tab Separated Value file with columns:
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- `subject gender status sample lane fastq1 fastq2` for step `mapping` with paired-end FASTQs
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- `subject gender status sample lane bam` for step `mapping` with unmapped BAMs
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- `subject gender status sample bam bai recaltable` for step `recalibrate` with BAMs
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- `subject gender status sample bam bai` for step `variantcalling` with BAMs
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- `subject sex status sample lane fastq1 fastq2` for step `mapping` with paired-end FASTQs
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- `subject sex status sample lane bam` for step `mapping` with unmapped BAMs
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- `subject sex status sample bam bai recaltable` for step `recalibrate` with BAMs
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- `subject sex status sample bam bai` for step `variantcalling` with BAMs
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The content of these columns is quite straight-forward:
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- `subject` designate the subject, it should be the ID of the Patient, and it must design only one patient
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- `gender` is the gender of the Patient, (XX or XY)
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- `sex` are the sex chromosomes of the Patient, (XX or XY)
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- `status` is the status of the Patient, (0 for Normal or 1 for Tumor)
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- `sample` designate the Sample, it should be the ID of the sample (it is possible to have more than one tumor sample for each patient, i.e. a tumor and a relapse), it must design only one sample
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- `lane` is used when the sample is multiplexed on several lanes, it must be unique for each lane in the same sample

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