首页|Finding a suitable library size to call variants in RNA-seq

Finding a suitable library size to call variants in RNA-seq

Flensburg Christoffer Speed Terence P Quaglieri Anna Majewski Ian J

DOI：10.1101/2019.12.18.881870

来源：

bioRxiv

Finding a suitable library size to call variants in RNA-seq

Flensburg Christoffer ¹Speed Terence P ²Quaglieri Anna ¹Majewski Ian J¹

作者信息

1. Walter and Eliza Hall Institute of Medical Research||Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne
2. Walter and Eliza Hall Institute of Medical Research||Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne||Department of Mathematics and Statistics, University of Melbourne
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Key words

cancer RNA-Seq/variant calling/library size/sequencing depth

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Flensburg Christoffer,Speed Terence P,Quaglieri Anna,Majewski Ian J.Finding a suitable library size to call variants in RNA-seq[EB/OL].(2025-03-28)[2025-12-13].https://www.biorxiv.org/content/10.1101/2019.12.18.881870.

学科分类

肿瘤学/生物科学研究方法、生物科学研究技术/基础医学

首发时间： 2025-03-28

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Finding a suitable library size to call variants in RNA-seq

Finding a suitable library size to call variants in RNA-seq

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