[ 原始碼： htseq ]
套件：python-htseq（0.11.2-1）
Python 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.
This package contains the Python 2 module.
負責填實 python-htseq 的套件
- python3-htseq
- Python3 high-throughput genome sequencing read analysis utilities
其他與 python-htseq 有關的套件
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- dep: libc6 (>= 2.14) [amd64]
- GNU C 函式庫：共用函式庫
同時作為一個虛擬套件由這些套件填實： libc6-udeb
- dep: libc6 (>= 2.17) [arm64]
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- dep: libgcc1 (>= 1:3.0)
- GCC 支援函式庫
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- dep: libstdc++6 (>= 5)
- GNU Standard C++ Library v3
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- dep: python
- interactive high-level object-oriented language (Python2 version)
- dep: python (<< 2.8)
- dep: python (>= 2.7)
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- dep: python-numpy
- Numerical Python adds a fast array facility to the Python language
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- dep: python-pysam
- interface for the SAM/BAM sequence alignment and mapping format (Python 2)