NGS allele counts versus called genotypes for testing genetic association
RNA sequence data are commonly summarized as read counts. By contrast, so far there is no alternative to genotype calling for investigating the relationship between genetic variants determined by next-generation sequencing (NGS) and a phenotype of interest. Here we propose and evaluate the direct an...
Main Authors: | Rosa González Silos, Christine Fischer, Justo Lorenzo Bermejo |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2022-01-01
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Series: | Computational and Structural Biotechnology Journal |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2001037022002951 |
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