Balík: python3-htseq (2.0.5-2 a iné)

[ Zdroj: htseq  ]

Python3 high-throughput genome sequencing read analysis utilities

HTSeq can be used to performing a number of common analysis tasks when working with high-throughput genome sequencing reads:

  * Getting statistical summaries about the base-call quality scores to
    study the data quality.
  * Calculating a coverage vector and exporting it for visualization in
    a genome browser.
  * Reading in annotation data from a GFF file.
  * Assigning aligned reads from an RNA-Seq experiments to exons and
    genes.

Ostatné balíky súvisiace s balíkom python3-htseq

• dep: libc6 (>= 2.4)

  knižnica GNU C - zdieľané knižnice
  tiež virtuálny balík poskytovaný balíkom libc6-udeb

• dep: libgcc-s1 (>= 3.5)

  podporná knižnica GCC

• dep: libstdc++6 (>= 13.1)

  štandardná knižnica C++ GNU v3

• dep: python3

  interactive high-level object-oriented language (default python3 version)

  dep: python3 (<< 3.13)

  dep: python3 (>= 3.12~)

• dep: python3-numpy (>= 1:1.25.0)

  Fast array facility to the Python language (Python 3)

• dep: python3-numpy-abi9

  virtuálny balík poskytovaný balíkom python3-numpy

• dep: python3-pysam

  interface for the SAM/BAM sequence alignment and mapping format (Python 3)

Stiahnuť python3-htseq

Stiahnuť pre všetky dostupné architektúry

Architektúra	Verzia	Veľkosť balíka	Nainštalovaná veľkosť	Súbory
armhf	2.0.5-2+b1	270.9 kB	790.0 kB	[zoznam súborov]