Balík: pbhoney (15.8.24+dfsg-3)

[ Zdroj: pbsuite  ]

genomic structural variation discovery

PBHoney is an implementation of two variant-identification approaches designed to exploit the high mappability of long reads (i.e., greater than 10,000 bp). PBHoney considers both intra-read discordance and soft-clipped tails of long reads to identify structural variants.

PBHoney is part of the PBSuite.

Ostatné balíky súvisiace s balíkom pbhoney

• dep: blasr (>= 5.3)

  mapping single-molecule sequencing reads

• dep: python

  interaktívny vysokoúrovňový objektovo orientovaný jazyk (verzia python2)

• dep: python-h5py

  rozhranie k hdf5 na všeobecné účely pre Python 2

• dep: python-intervaltree-bio

  Interval tree convenience classes for genomic data -- Python 2 library

• dep: python-networkx

  nástroj na tvorbu, manipuláciu a študovanie komplexných sietí

• dep: python-numpy

  Numerical Python pridáva schopnosti rýchlych polí do jazyka Python

• dep: python-pbbanana (= 15.8.24+dfsg-3)

  additional utilities for the pbsuite

• dep: python-pbsuite-utils (= 15.8.24+dfsg-3)

  software for Pacific Biosciences sequencing data -- Python utilities

• dep: python-pysam (>= 0.8.0)

  interface for the SAM/BAM sequence alignment and mapping format (Python 2)

• dep: samtools

  processing sequence alignments in SAM, BAM and CRAM formats

• rec: pbdagcon

  sequence consensus using directed acyclic graphs

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