[ 源代码： htseq ]
软件包：python3-htseq（2.0.5-2 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
|
|
|
|
-
- dep: libc6 (>= 2.4)
- 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
-
- dep: libgcc-s1 (>= 3.5)
- GCC 支持库
-
- dep: libstdc++6 (>= 13.1)
- GNU 标准 C++ 库，第3版
-
- 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
- 本虚包由这些包填实： python3-numpy
-
- dep: python3-pysam
- interface for the SAM/BAM sequence alignment and mapping format (Python 3)