Tag search tools for the detection of structural variants

Genetics

Original work

Detection of copy number variation from low-coverage whole-genome sequencing data

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Copy number variation (CNV) is a form of structural variant that leads to an abnormal number of copies of genomic regions in a cell. Next-generation-sequencing...

Keywords: copy number variations, detection of copy number variations., detection of the structural variants, structural variants, tools for the detection of structural variants

newslab 2021, 02 : 53 - 57

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