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Text replace - "Personal genomics" to "Personalised medicine"
{{Bioinformatics application
|sw summary=mrCaNaVaR is a copy number caller that analyzes the next-generation sequence mapping read depth to discover large segmental duplications and deletions. It also has the capability of predicting absolute copy numbers of genomic intervals.
|bio domain=Genomics, Personal genomicsPersonalised medicine, Copy number estimation,
|bio method=Read depth analysis
|bio tech=Illumina,
