Article

Red Panda: A novel method for detecting variants in single-cell RNA sequencing

2020-01-09

Abstract excerpt

Single-cell sequencing enables us to better understand genetic diseases, such as cancer or autoimmune disorders, which are often affected by changes in rare cells. Currently, no existing software is aimed at identifying single nucleotide variations or micro (1-50bp) insertions and deletions in single-cell RNA sequencing (scRNA-seq) data. Generating high-quality variant data is vital to the study of the aforementio...

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Literature Corpus work: cd0da2d4-55ef-5c0a-9def-c8731361099d
DOI: 10.1101/2020.01.08.898874

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