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PyDESeq2:一个用于批量 RNA-seq 差异表达分析的 Python 包。

PyDESeq2: a python package for bulk RNA-seq differential expression analysis.

机构信息

Owkin France, Paris, 75009, France.

出版信息

Bioinformatics. 2023 Sep 2;39(9). doi: 10.1093/bioinformatics/btad547.


DOI:10.1093/bioinformatics/btad547
PMID:37669147
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10502239/
Abstract

SUMMARY: We present PyDESeq2, a python implementation of the DESeq2 workflow for differential expression analysis on bulk RNA-seq data. This re-implementation yields similar, but not identical, results: it achieves higher model likelihood, allows speed improvements on large datasets, as shown in experiments on TCGA data, and can be more easily interfaced with modern python-based data science tools. AVAILABILITY AND IMPLEMENTATION: PyDESeq2 is released as an open-source software under the MIT license. The source code is available on GitHub at https://github.com/owkin/PyDESeq2 and documented at https://pydeseq2.readthedocs.io. PyDESeq2 is part of the scverse ecosystem.

摘要

摘要:我们介绍了 PyDESeq2,这是一个用于批量 RNA-seq 数据差异表达分析的 DESeq2 工作流程的 Python 实现。这个重新实现的结果相似,但不完全相同:它实现了更高的模型似然性,允许在大型数据集上提高速度,如在 TCGA 数据上的实验所示,并且可以更轻松地与现代基于 Python 的数据科学工具接口。

可用性和实现:PyDESeq2 作为 MIT 许可证下的开源软件发布。源代码可在 GitHub 上的 https://github.com/owkin/PyDESeq2 获得,并在 https://pydeseq2.readthedocs.io 上有文档说明。PyDESeq2 是 scverse 生态系统的一部分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74c4/10502239/7f88598923b9/btad547f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74c4/10502239/7f88598923b9/btad547f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74c4/10502239/7f88598923b9/btad547f1.jpg

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本文引用的文献

[1]
The scverse project provides a computational ecosystem for single-cell omics data analysis.

Nat Biotechnol. 2023-5

[2]
Squidpy: a scalable framework for spatial omics analysis.

Nat Methods. 2022-2

[3]
SciPy 1.0: fundamental algorithms for scientific computing in Python.

Nat Methods. 2020-2-3

[4]
RNA sequencing: the teenage years.

Nat Rev Genet. 2019-7-24

[5]
Heavy-tailed prior distributions for sequence count data: removing the noise and preserving large differences.

Bioinformatics. 2019-6-1

[6]
SCANPY: large-scale single-cell gene expression data analysis.

Genome Biol. 2018-2-6

[7]
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2.

Genome Biol. 2014

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