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Workshop: Detailed Analysis of Cancer Mutations using Next Generation Sequencing (NGS)
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In this webinar, we will get insights about :
Tools for Genomic Data Analysis to interrogate genomic variations for cancer studies and to perform somatic and Germline variant detection, driver and passenger mutations, copy Number Variation as well as for Tumor sub-clonal deconvolution.
Tools for Genomic Data Analysis to interrogate genomic variations for cancer studies and to perform somatic and Germline variant detection, driver and passenger mutations, copy Number Variation as well as for Tumor sub-clonal deconvolution.
Workshop: Detailed Analysis of Cancer Mutations using Next Generation Sequencing (NGS)
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