Jun 3, 2015

Cpipe: a shared variant detection pipeline designed for diagnostic settings

BioRxiv : the Preprint Server for Biology
Simon P Sadedin

Abstract

The benefits of implementing high throughput sequencing in the clinic are quickly becoming apparent. However, few freely available bioinformatics pipelines have been built from the ground up with clinical genomics in mind. Here we present Cpipe, a pipeline designed specifically for clinical genetic disease diagnostics. Cpipe was developed by the Melbourne Genomics Health Alliance, an Australian initiative to promote common approaches to genomics across healthcare institutions. As such, Cpipe has been designed to provide fast, effective and reproducible analysis, while also being highly flexible and customisable to meet the individual needs of diverse clinical settings. Cpipe is being shared with the clinical sequencing community as an open source project and is available at http://cpipeline.org.

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Mentioned in this Paper

Clinical Genomics
Clinic
Health Alliances
Bio-Informatics
Genomics
Sequencing
Clinical Trials
Analysis
High-Throughput RNA Sequencing
Hereditary Diseases

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