$ dsh-bio --help
usage:
dsh-bio [command] [args]

commands:
  bin-fastq-quality-scores    bin quality scores from files in FASTQ format
  compress-bed    compress features in BED format to splittable bgzf or bzip2 compression codecs
  compress-fasta    compress sequences in FASTA format to splittable bgzf or bzip2 compression codecs
  compress-fastq    compress sequences in FASTQ format to splittable bgzf or bzip2 compression codecs
  compress-gaf    compress alignments in GAF format to splittable bgzf or bzip2 compression codecs
  compress-gfa1    compress assembly in GFA 1.0 format to splittable bgzf or bzip2 compression codecs
  compress-gfa2    compress assembly in GFA 2.0 format to splittable bgzf or bzip2 compression codecs
  compress-gff3    compress features in GFF3 format to splittable bgzf or bzip2 compression codecs
  compress-paf    compress alignments in PAF format to splittable bgzf or bzip2 compression codecs
  compress-rgfa    compress assembly in rGFA format to splittable bgzf or bzip2 compression codecs
  compress-sam    compress alignments in SAM format to splittable bgzf or bzip2 compression codecs
  compress-vcf    compress variants and genotypes in VCF format to splittable bgzf or bzip2 compression codecs
  create-sequence-dictionary    create a SequenceDictionary from DNA sequences in FASTA format
  disinterleave-fastq    convert interleaved FASTQ format into first and second DNA sequence files in FASTQ format
  downsample-fastq    downsample DNA sequences from files in FASTQ format
  downsample-interleaved-fastq    downsample DNA sequences from a file in interleaved FASTQ format
  export-segments    export assembly segment sequences in GFA 1.0 format to FASTA format
  extract-fasta    extract matching DNA or protein sequences in FASTA format
  extract-fastq    extract matching DNA sequences in FASTQ format
  extract-fastq-by-length    extract DNA sequences in FASTQ format with a range of lengths
  fasta-to-fastq    convert DNA sequences in FASTA format to FASTQ format
  fasta-to-text    convert DNA or protein sequences in FASTA format to tab-separated values (tsv) text format
  fastq-description    output description lines from DNA sequences in FASTQ format
  fastq-sequence-length    output sequence lengths from DNA sequences in FASTQ format
  fastq-to-bam    convert DNA sequences in FASTQ format to unaligned BAM format
  fastq-to-fasta    convert DNA sequences in FASTQ format to FASTA format
  fastq-to-text    convert DNA sequences in FASTQ format to tab-separated values (tsv) text format
  filter-bed    filter features in BED format
  filter-fasta    filter sequences in FASTA format
  filter-fastq    filter sequences in FASTQ format
  filter-gaf    filter alignments in GAF format
  filter-gfa1    filter assembly in GFA 1.0 format
  filter-gfa2    filter assembly in GFA 2.0 format
  filter-gff3    filter features in GFF3 format
  filter-paf    filter alignments in PAF format
  filter-rgfa    filter assembly in rGFA format
  filter-sam    filter alignments in SAM format
  filter-vcf    filter variants in VCF format
  gfa1-to-gfa2    convert GFA 1.0 format to GFA 2.0 format
  identify-gfa1    add identifier annotation to records in GFA 1.0 format
  interleave-fastq    convert first and second DNA sequence files in FASTQ format to interleaved FASTQ format
  interleaved-fastq-to-bam    convert DNA sequences in interleaved FASTQ format to unaligned BAM format
  links-to-cytoscape-edges    convert links in GFA 1.0 format to edges.txt format for Cytoscape
  links-to-property-graph    convert links in GFA 1.0 format to property graph CSV format
  list-filesystems    list filesystem providers
  reassemble-paths    reassemble paths in GFA 1.0 format from traversal records
  remap-dbsnp    remap DB Type=String flags in VCF format to DB Type=Flag and dbsnp Type=String fields
  remap-phase-set    remap PS Type=String phase set ids in VCF format to PS Type=Integer
  rename-bed-references    rename references in BED files
  rename-gff3-references    rename references in GFF3 files
  rename-vcf-references    rename references in VCF files
  segments-to-cytoscape-nodes    convert segments in GFA 1.0 format to nodes.txt format for Cytoscape
  segments-to-property-graph    convert segments in GFA 1.0 format to property graph CSV format
  split-bed    split files in BED format
  split-fasta    split files in FASTA format
  split-fastq    split files in FASTQ format
  split-gaf    split files in GAF format
  split-gff3    split files in GFF3 format
  split-interleaved-fastq    split files in interleaved FASTQ format
  split-paf    split files in PAF format
  split-sam    split files in SAM format
  split-vcf    split files in VCF format
  text-to-fasta    convert DNA or protein sequences in tab-separated values (tsv) text format to FASTA format
  text-to-fastq    convert DNA sequences in tab-separated values (tsv) text format to FASTQ format
  traversals-to-cytoscape-edges    convert traversals in GFA 1.0 format to edges.txt format for Cytoscape
  traversals-to-property-graph    convert traversals in GFA 1.0 format to property graph CSV format
  traverse-paths    traverse paths in GFA 1.0 format
  truncate-fasta    truncate DNA or protein sequences in FASTA format
  truncate-paths    truncate paths in GFA 1.0 format
  variant-table-to-vcf    convert Ensembl variant table to VCF format
  vcf-pedigree    extract a pedigree from VCF format
  vcf-samples    extract samples from VCF format

arguments:
   -a, --about  display about message [optional]
   -v, --version  display about message [optional]
   -h, --help  display help message [optional]


$ dsh-bio split-bed --help
usage:
dsh-split-bed -r 100 -i foo.bed.gz

arguments:
   -a, --about  display about message [optional]
   -h, --help  display help message [optional]
   -i, --input-path [interface java.nio.file.Path]  input BED path, default stdin [optional]
   -b, --bytes [class java.lang.String]  split input path at next record after each n bytes [optional]
   -r, --records [class java.lang.Long]  split input path after each n records [optional]
   -p, --prefix [class java.lang.String]  output file prefix [optional]
   -d, --left-pad [class java.lang.Integer]  left pad split index in output file name [optional]
   -s, --suffix [class java.lang.String]  output file suffix, e.g. .bed.gz [optional]

$ dsh-split-bed --help
usage:
dsh-split-bed -r 100 -i foo.bed.gz

arguments:
   -a, --about  display about message [optional]
   -h, --help  display help message [optional]
   -i, --input-path [interface java.nio.file.Path]  input BED path, default stdin [optional]
   -b, --bytes [class java.lang.String]  split input path at next record after each n bytes [optional]
   -r, --records [class java.lang.Long]  split input path after each n records [optional]
   -p, --prefix [class java.lang.String]  output file prefix [optional]
   -d, --left-pad [class java.lang.Integer]  left pad split index in output file name [optional]
   -s, --suffix [class java.lang.String]  output file suffix, e.g. .bed.gz [optional]

$ dsh-bio filter-bed -i input.bed --script "r.getChrom() == 1 && r.getScore() > 10.0"

$ conda install dsh-bio

$ brew install brewsci/bio/dsh-bio

$ docker pull quay.io/biocontainers/dsh-bio:{tag}