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reads to genome, pangenome graphs, summarize and analyze

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panscape

  • from reads to alignments to pangenome, metagenome inclduing the genome annotation using the nanopore and pacbio under one rust binary
  • this will also creates the pangenome database and also the pangenome reads database for rest api.
  • this code will be updated regularly.
cargo build
gauravsablok@genome panscape main ? ./target/debug/panscape -h
panscape: analyzing pangenomes from reads to stats

Usage: panscape <COMMAND>

Commands:
 fasta-convert         convert into fasta
 clipper-align         clipping the regions from the fastq
 scanner               scans the reads for the motifs single occurence
 motifcatcher          motif plus upstream and the downstream
 selectedreads         selected reads writer
 filterreads           filter the reads prior to the length
 clip-seq              remove the clip regions from the reads
 multi-clip-seq        remove the multitags for the fastqfile
 pangenome             assemble pangenome
 minimap               annotate reads
 stat                  annotated stats for your file
 pangenome-summarize   pangenome pre-computed alignment
 read-multisearch      multisearch reads across the reads
 paf-annotate          annotate your pangenome paf alignment using gtf
 harmonicmean          estimate the harmonic mean from the pangenome
 pangenome-matcher     pangenome matcher
 pan-arc               pangenome annotator
 snatcher              extract specific region from paf alignment
 precomputed-paf       generate stats from precomputed paf
 precompute-cds        extract the coding regions from the precomputed pangenome
 graph                 graph analyzer
 pangenome-bed         Pangenome bed constructor
 intergenic-noncoding  Intergenic extractor
 pan-reads-database    pangenome database
 help                  Print this message or the help of the given subcommand(s)

Options:
 -h, --help     Print help
 -V, --version  Print version

Gaurav Sablok

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