Article
Detection of isoforms and genomic alterations by high-throughput full-length single-cell RNA sequencing in ovarian cancer
2022-12-14
Abstract excerpt
Understanding the complex background of cancer requires genotype-phenotype information in single-cell resolution. Here, we perform long-read single-cell RNA sequencing (scRNA-seq) on clinical samples from three ovarian cancer patients presenting with omental metastasis and increase the PacBio sequencing depth to 12,000 reads per cell. Our approach captures 152,000 isoforms, of which over 52,000 are novel. Isoform-...
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Identifiers and source
- Literature Corpus work
- 31c6912d-3529-5af4-b7c3-5ae89b7156f1
- DOI
- 10.1101/2022.12.12.520051
