Preprocessing Sequence Coverage Data for More Precise Detection of Copy Number Variations
Sign Up to like & getrecommendations! Published in 2020 at "IEEE/ACM Transactions on Computational Biology and Bioinformatics"
DOI: 10.1109/tcbb.2018.2869738
Abstract: Copy number variation (CNV) is a type of genomic/genetic variation that plays an important role in phenotypic diversity, evolution, and disease susceptibility. Next generation sequencing (NGS) technologies have created an opportunity for more accurate detection… read more here.
Keywords: sequence coverage; copy number; detection; precise detection ... See more keywords