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Bridging the gap between R and Python in bulk transcriptomic data analysis with InMoose

delete2025-05-24
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OA
AI
M
Maximilien Colange *
G
Guillaume Appé
L
Léa Meunier
S
Solène Weill
W
W. Evan Johnson
A
Akpéli Nordor
A
Abdelkader Behdenna
DOI:10.1038/s41598-025-03376-ydelete
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摘要

摘要

En 中文
我们介绍InMoose,一个面向组学数据分析的开源Python环境。我们展示了其在批量转录组数据分析方面的能力。由于Python的广泛应用,它已成为数据科学、机器学习或人工智能(AI)等日益重要的生物信息学流程领域的事实标准。作为一种通用语言,Python也因其多功能性和可扩展性而备受认可。InMoose旨在将历史上用R编写的先进工具引入Python生态系统。InMoose专注于为R工具提供即插即用的替代方案,以确保基于R和基于Python的流程之间的一致性和可重复性。第一阶段开发专注于批量转录组数据,当前功能涵盖数据模拟、批次效应校正以及差异分析和元分析。

期刊

Scientific Reports 封面图
Scientific Reports
IF:
3.9
论文数:
28.3W
被引数:
83.5W

机构

E
epigene labs
学者数:
6
论文数: 2
被引数: 0
R
Rutgers State Univ
学者数:
1.1K
论文数: 742
被引数: 296
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