Tools and Databases
Developments in FINDbase worldwide database for clinically relevant genomic variation allele frequencies
Papadopoulos P, et al. Nucleic Acids Res 2013 Nov
ICO Amplicon NGS data analysis: A web tool for variant detection in common high-risk hereditary cancer genes analyzed by Amplicon GS Junior next generation sequencing
Lopez-Doriga A, et al. Hum Mutat 2013 Nov
A complete public domain family genomics dataset
, Haldane's Sieve, Nov 14
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