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Structural variants in the barley gene pool: precision and sensitivity to detect them using short-read sequencing and their association with gene expression and phenotypic variation

2022-04-25

Abstract excerpt

<h4>ABSTRACT</h4> In human genetics, several studies have shown that phenotypic variation is more likely to be caused by structural variants (SV) than by single nucleotide variants (SNV). However, accurate while cost-efficient discovery of SV in complex genomes remains challenging. The objectives of our study were to (i) facilitate SV discovery studies by benchmarking SV callers and their combinations with respec...

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Literature Corpus work
a64b0367-0d8d-5008-a1b9-75cd9cc2fb9a
DOI
10.1101/2022.04.25.489331
Open publication

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Structural variants in the barley gene pool: precision and sensitivity to detect them using short-read sequencing and their association with gene expression and phenotypic variationDOI 10.1101/2022.04.25.489331
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