Analysing high-throughput sequencing data in Python with HTSeq 2.0

HTSeq 2.0 provides a more extensive application programming interface including a new representation for sparse genomic data, enhancements for htseq-count to suit single-cell omics, a new script for data using cell and molecular barcodes, improved documentation, testing and deployment, bug fixes and...

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Vydáno v:Bioinformatics (Oxford, England) Ročník 38; číslo 10; s. 2943 - 2945
Hlavní autoři: Putri, Givanna H, Anders, Simon, Pyl, Paul Theodor, Pimanda, John E, Zanini, Fabio
Médium: Journal Article
Jazyk:angličtina
Vydáno: England Oxford University Press 13.05.2022
Témata:
Applications Notes
Documentation
Genomics
High-Throughput Nucleotide Sequencing
Licensure
Software
ISSN:1367-4803, 1367-4811
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Shrnutí:HTSeq 2.0 provides a more extensive application programming interface including a new representation for sparse genomic data, enhancements for htseq-count to suit single-cell omics, a new script for data using cell and molecular barcodes, improved documentation, testing and deployment, bug fixes and Python 3 support. HTSeq 2.0 is released as an open-source software under the GNU General Public License and is available from the Python Package Index at https://pypi.python.org/pypi/HTSeq. The source code is available on Github at https://github.com/htseq/htseq. Supplementary data are available at Bioinformatics online.
ISSN:1367-4803
1367-4811
DOI:10.1093/bioinformatics/btac166