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'COV'COP' allows to detect CNVs responsible for inherited diseases among amplicons sequencing data.
Bioinformatics 2017 May 16
Summary: In order to help molecular geneticists to rapidly identify CNVs responsible for inherited diseases among amplicons sequencing data generated by NGS, we designed a user-friendly tool ' Cov'Cop '. Using the run's coverage file provided by the sequencer, Cov'Cop simultaneously analyzes all the patients of the run using a two-stage algorithm containing correction and normalization levels and provides an easily understandable output, showing with various colors, potentially deleted and duplicated amplicons.
Availability and Implementation: https://git.unilim.fr/merilp02/CovCop.
Contact: [email protected].
Supplementary information: Supplementary data are available at Bioinformatics online.
Availability and Implementation: https://git.unilim.fr/merilp02/CovCop.
Contact: [email protected].
Supplementary information: Supplementary data are available at Bioinformatics online.
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