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Mutation Detection and CNV Analysis for Illumina Sequencing data from HaloPlex Target Enrichment Panels using NextGENe Software for Clinical Research
29 May 2013

The HaloPlex Target Enrichment System allows for rapid targeted sequencing and library preparation in a single-tube reaction with no need for library preparation and support for up to 96 barcoded samples in one reaction. This application note covers analysis of this data when sequencing is performed on Illumina HiSeq or MiSeq sequencing systems.

Agilent Technologies

Tags: target-enrichment, copy number variation, mutation analysis

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