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Ioncopy: an R Shiny app to call copy number alterations in targeted NGS data
Background Somatic copy number alterations (CNAs) contribute to the clinically targetable aberrations in the tumor genome. For both routine diagnostics and biomarkers research,... -
RGmatch: matching genomic regions to proximal genes in omics data integration
© The Author(s). 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License... -
Enabling precision medicine via standard communication of HTS provenance, ana...
A personalized approach based on a patient's or pathogen’s unique genomic sequence is the foundation of precision medicine. Genomic findings must be robust and reproducible, and...
