Comprehensive characterization of single-cell full-length isoforms in human and mouse with long-read sequencing.
Tian L., Jabbari JS., Thijssen R., Gouil Q., Amarasinghe SL., Voogd O., Kariyawasam H., Du MRM., Schuster J., Wang C., Su S., Dong X., Law CW., Lucattini A., Prawer YDJ., Collar-Fernández C., Chung JD., Naim T., Chan A., Ly CH., Lynch GS., Ryall JG., Anttila CJA., Peng H., Anderson MA., Flensburg C., Majewski I., Roberts AW., Huang DCS., Clark MB., Ritchie ME.
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.