[ 源代码： htseq ]
软件包：python3-htseq（2.0.9+dfsg-1 以及其他的）
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.
其他与 python3-htseq 有关的软件包
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- dep: libc6 (>= 2.17)
- GNU C 语言运行库：共享库
同时作为一个虚包由这些包填实： libc6-udeb
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- dep: libgcc-s1 (>= 3.0)
- GCC 支持库
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- dep: libstdc++6 (>= 13.1)
- GNU 标准 C++ 库，第3版
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- dep: python3
- 交互式高级面向对象语言（默认 python3 版本）
- dep: python3 (<< 3.14)
- dep: python3 (>= 3.12~)
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- dep: python3-numpy
- Fast array facility to the Python language (Python 3)
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- dep: python3-numpy2-abi0
- 软件包暂时不可用
- 或者 python3-numpy-abi9
- 本虚包由这些包填实： python3-numpy
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- dep: python3-pysam
- interface for the SAM/BAM sequence alignment and mapping format (Python 3)