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Article

SIngle cell level Genotyping Using scRna Data (SIGURD)

2024-07-19

Abstract excerpt

<h4>ABSTRACT</h4> <h4>Motivation</h4> By accounting for variants within measured transcripts, it is possible to evaluate the status of somatic variants using single-cell RNA-sequencing (scRNA-seq) and to characterize their clonality. However, the sparsity (very few reads per transcript) or bias in protocols (favoring 3’ ends of the transcripts) makes the chance of capturing somatic variants very unlikely. This c...

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Identifiers and source

Literature Corpus work
f7730a9e-7cc2-56ad-a82f-af0a985e6358
DOI
10.1101/2024.07.16.603737
Open publication

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SIngle cell level Genotyping Using scRna Data (SIGURD)DOI 10.1101/2024.07.16.603737
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