diff --git a/index.md b/index.md index 849097e3..64000a40 100644 --- a/index.md +++ b/index.md @@ -45,31 +45,32 @@ You can call `harpy` without any arguments (or with `--help`) to print the docst Documentation: https://pdimens.github.io/harpy/ -╭─ Options ───────────────────────────────────────────────────────────────╮ -│ --version Show the version and exit. │ -│ --help -h Show this message and exit. │ -╰─────────────────────────────────────────────────────────────────────────╯ -╭─ workflows ─────────────────────────────────────────────────────────────╮ -│ demultiplex Demultiplex haplotagged FASTQ files │ -│ qc Remove adapters and quality-control sequences │ -│ align Align sample sequences to a reference genome │ -│ snp Call SNPs and small indels on alignments │ -│ sv Call large structural variants on alignments │ -│ impute Impute genotypes using variants and alignments │ -│ phase Phase SNPs into haplotypes │ -│ simulate Simulate variants or linked-reads from a genome │ -│ assembly Create an assembly from linked-reads │ -│ metassembly Create a metassembly from linked-reads │ -╰─────────────────────────────────────────────────────────────────────────╯ -╭─ Other Commands ────────────────────────────────────────────────────────╮ -│ deconvolve Resolve clashing barcodes from different molecules │ -│ hpc Profile templates for cluster job submissions │ -│ imputeparams Create a template imputation parameter file │ -│ popgroup Create a template grouping file for samples │ -│ preflight File format checks for haplotag data │ -│ resume Resume a workflow from an existing Harpy directory │ -│ view View a workflow log, config, or snakefile │ -╰─────────────────────────────────────────────────────────────────────────╯ +╭─ Options ─────────────────────────────────────────────────────────────╮ +│ --version Show the version and exit. │ +│ --help -h Show this message and exit. │ +╰───────────────────────────────────────────────────────────────────────╯ +╭─ workflows ───────────────────────────────────────────────────────────╮ +│ align Align sample sequences to a reference genome │ +│ assembly Create an assembly from linked-reads │ +│ demultiplex Demultiplex haplotagged FASTQ files │ +│ impute Impute genotypes using variants and alignments │ +│ metassembly Create a metassembly from linked-reads │ +│ phase Phase SNPs into haplotypes │ +│ qc Remove adapters and quality-control sequences │ +│ simulate Simulate variants or linked-reads from a genome │ +│ snp Call SNPs and small indels on alignments │ +│ sv Call large structural variants on alignments │ +╰───────────────────────────────────────────────────────────────────────╯ +╭─ Other Commands ──────────────────────────────────────────────────────╮ +│ deconvolve Resolve clashing barcodes from different molecules │ +│ downsample Downsample data by barcode │ +│ hpc Profile templates for cluster job submissions │ +│ imputeparams Create a template imputation parameter file │ +│ popgroup Create a template grouping file for samples │ +│ preflight File format checks for haplotag data │ +│ resume Resume a workflow from an existing Harpy directory │ +│ view View a workflow log, config, or snakefile │ +╰───────────────────────────────────────────────────────────────────────╯ ``` ## Typical Linked-Read Workflows