1,009
edits
Changes
m
Text replace - "Personal genomics" to "Personalised medicine"
{{Bioinformatics application
|sw summary=CopySeq analyzes the depth-of-coverage of whole genome resequencing data to predict CNVs and to infer quantitative locus copy-number genotypes.
|bio domain=Structural variation, Copy number estimation, Genotyping, Personal genomicsPersonalised medicine,
|bio tech=Illumina
|created at=Weizmann Institute of Science, EMBL