Comprehensive characterization of single-cell full-length isoforms in human and mouse with long-read sequencing.
Genome Biol
; 22(1): 310, 2021 11 11.
Article
em En
| MEDLINE
| ID: mdl-34763716
A modified Chromium 10x droplet-based protocol that subsamples cells for both short-read and long-read (nanopore) sequencing together with a new computational pipeline (FLAMES) is developed to enable isoform discovery, splicing analysis, and mutation detection in single cells. We identify thousands of unannotated isoforms and find conserved functional modules that are enriched for alternative transcript usage in different cell types and species, including ribosome biogenesis and mRNA splicing. Analysis at the transcript level allows data integration with scATAC-seq on individual promoters, improved correlation with protein expression data, and linked mutations known to confer drug resistance to transcriptome heterogeneity.
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Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Isoformas de Proteínas
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Sequenciamento por Nanoporos
Limite:
Animals
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Humans
Idioma:
En
Ano de publicação:
2021
Tipo de documento:
Article