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Analysing high-throughput sequencing data in Python with HTSeq 2.0
SUMMARY: 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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9113351/ https://www.ncbi.nlm.nih.gov/pubmed/35561197 http://dx.doi.org/10.1093/bioinformatics/btac166 |
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author | Putri, Givanna H Anders, Simon Pyl, Paul Theodor Pimanda, John E Zanini, Fabio |
author_facet | Putri, Givanna H Anders, Simon Pyl, Paul Theodor Pimanda, John E Zanini, Fabio |
author_sort | Putri, Givanna H |
collection | PubMed |
description | SUMMARY: 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. AVAILABILITY AND IMPLEMENTATION: 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 INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-9113351 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-91133512022-05-18 Analysing high-throughput sequencing data in Python with HTSeq 2.0 Putri, Givanna H Anders, Simon Pyl, Paul Theodor Pimanda, John E Zanini, Fabio Bioinformatics Applications Notes SUMMARY: 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. AVAILABILITY AND IMPLEMENTATION: 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 INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2022-03-21 /pmc/articles/PMC9113351/ /pubmed/35561197 http://dx.doi.org/10.1093/bioinformatics/btac166 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Applications Notes Putri, Givanna H Anders, Simon Pyl, Paul Theodor Pimanda, John E Zanini, Fabio Analysing high-throughput sequencing data in Python with HTSeq 2.0 |
title | Analysing high-throughput sequencing data in Python with HTSeq 2.0 |
title_full | Analysing high-throughput sequencing data in Python with HTSeq 2.0 |
title_fullStr | Analysing high-throughput sequencing data in Python with HTSeq 2.0 |
title_full_unstemmed | Analysing high-throughput sequencing data in Python with HTSeq 2.0 |
title_short | Analysing high-throughput sequencing data in Python with HTSeq 2.0 |
title_sort | analysing high-throughput sequencing data in python with htseq 2.0 |
topic | Applications Notes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9113351/ https://www.ncbi.nlm.nih.gov/pubmed/35561197 http://dx.doi.org/10.1093/bioinformatics/btac166 |
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