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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 variantsvariation, Copy number estimation, Genotyping, Personal genomicsPersonalised medicine, |bio tech=Illumina/Solexa|created at=Weizmann Institute of Science, EMBL
|maintained=Yes
|input format=BAM, SVF|output format=tabTab-delimited file|language=Java 1.6, R|os=Mac OS X 10.5, Linux,
}}
== Description ==