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M3Drop: dropout-based feature selection for scRNASeq.
Andrews, Tallulah S; Hemberg, Martin.
Afiliação
  • Andrews TS; Department of Cellular Genetics, Wellcome Trust Sanger Institute, Hinxton, Cambridgshire, UK.
  • Hemberg M; Department of Cellular Genetics, Wellcome Trust Sanger Institute, Hinxton, Cambridgshire, UK.
Bioinformatics ; 35(16): 2865-2867, 2019 08 15.
Article em En | MEDLINE | ID: mdl-30590489
ABSTRACT
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. AVAILABILITY AND IMPLEMENTATION M3Drop is freely available on github as an R package and is compatible with other popular scRNASeq tools https//github.com/tallulandrews/M3Drop. SUPPLEMENTARY INFORMATION Supplementary data are available at Bioinformatics online.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Software Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Software Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2019 Tipo de documento: Article