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Fix link in schema
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nextflow_schema.json

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"default": "null",
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"description": "Either paths or URLs to FASTQ/BAM data (must be surrounded with quotes). For paired end data, the path must use '{1,2}' notation to specify read pairs. Alternatively, a path to a TSV file (ending .tsv) containing file paths and sequencing/sample metadata. Allows for merging of multiple lanes/libraries/samples. Please see documentation for template.",
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"fa_icon": "fas fa-dna",
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"help_text": "There are two possible ways of supplying input sequencing data to nf-core/eager. The most efficient but more simplistic is supplying direct paths (with wildcards) to your FASTQ or BAM files, with each file or pair being considered a single library and each one run independently (e.g. for paired-end data: `--input '/<path>/<to>/*_{R1,R2}_*.fq.gz'`). TSV input requires creation of an extra file by the user (`--input '/<path>/<to>/eager_data.tsv'`) and extra metadata, but allows more powerful lane and library merging. Please see [usage docs](https://nf-co.re/eager/docs/usage#introduction) for detailed instructions and specifications."
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"help_text": "There are two possible ways of supplying input sequencing data to nf-core/eager. The most efficient but more simplistic is supplying direct paths (with wildcards) to your FASTQ or BAM files, with each file or pair being considered a single library and each one run independently (e.g. for paired-end data: `--input '/<path>/<to>/*_{R1,R2}_*.fq.gz'`). TSV input requires creation of an extra file by the user (`--input '/<path>/<to>/eager_data.tsv'`) and extra metadata, but allows more powerful lane and library merging. Please see [usage docs](https://nf-co.re/eager/docs/usage#input-specifications) for detailed instructions and specifications."
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},
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"udg_type": {
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"type": "string",

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