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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
Open publication

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Detection of isoforms and genomic alterations by high-throughput full-length single-cell RNA sequencing in ovarian cancerDOI 10.1101/2022.12.12.520051
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