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add downsample to the index
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pdimens committed Dec 13, 2024
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Expand Up @@ -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
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