期刊
BIOINFORMATICS
卷 35, 期 16, 页码 2865-2867出版社
OXFORD UNIV PRESS
DOI: 10.1093/bioinformatics/bty1044
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资金
- Wellcome Trust Sanger Core Funding
- Chan Zuckerberg Initiative DAF [183501]
Motivation: Most genomes contain thousands of genes, but for most functional responses, only a subset of those genes are relevant. To facilitate many single-cell RNASeq (scRNASeq) analyses the set of genes is often reduced through feature selection, i.e. by removing genes only subject to technical noise. Results: We present M3Drop, an R package that implements popular existing feature selection methods and two novel methods which take advantage of the prevalence of zeros (dropouts) in scRNASeq data to identify features. We show these new methods outperform existing methods on simulated and real datasets.
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