However, ES is not the first choice for detecting copy number variants (CNVs), which are typically deletions or duplications of DNA segments. CNVs cause a significant proportion of genetic disorders.
Clinical biobanks that combine genomic data with electronic health records (EHRs) have become powerful resources for ...
Copy number variation (CNV) refers to an increase or decrease in the number of copies of a DNA sequence in a genome, which can subsequently be implicit in promoting aberrant gene expression patterns ...
Clinical biobanks that combine genomic data with electronic health records (EHRs) have become powerful resources for ...
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