Article

DeepSSV: detecting somatic small variants in paired tumor and normal sequencing data with convolutional neural network

2019-03-30

Abstract excerpt

<h4>Motivation</h4> It is of considerable interest to detect somatic mutations in paired tumor and normal sequencing data. A number of callers that are based on statistical or machine learning approaches have been developed to detect somatic small variants. However, they take into consideration only limited information about the reference and potential variant allele in both samples at a candidate somatic site. A...

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Literature Corpus work: ab8efdd8-0b15-5537-9e05-8f7546f9292f
DOI: 10.1101/555680

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