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golden helix varseq vsclinical next gen sequencing variant interpretation acmg guidelines copy number variation cancer genetics amp guidelines ngs data clinical report genomics variant annotation variant analysis snp and variation suite ngs cnv copy number variants biotechnology somatic clinically relevant variants genomic data whole genome genetic analysis annotation sources whole exome whole genome sequencing genomic prediction cancerkb svs cancer vswarehouse clinical workflows oncogenicity cancer genes genetics tertiary analysis gblup variant evaluation acmg whole exome sequencing genomic analysis cnvs gene panels germline cancer biomarkers pharmacogenetics gwas genome wide association study exomes cnv calling snps precision medicine pharmacogenomics exome pharmaceutical single exome annotation catalog diagnostic clinical reports next generation sequencing biotech gene panel short read long read acmg variants amp structural variants secondary analysis gene fusions cloud computing trio analysis cnv detection pharma genetic mutations rare diseases ngs workflow bring your own cloud pgx indels snp data varseq 2.4.0 vs-cnv chromosomal microarrays agrigenomics cancerkb 2.0 phenotypes pacbio massive parallel sequencing wes cloud vscnv splice site variants database prenatal genetics prognostic clinical reports data analysis bioinformatics software pathogenicity bayes c k-fold cattle dataset bayes c-pi phenotypic traits biomarkers beagle imputation research translation vsreports loss of homozygosity loh variants cosmic vcf university of british columbia hereditary disease inheritance patterns molecular therapy digital health genetic software catfish large-n inherited diseases virtus diagnostics mark trinder stanford university department of genetics reza sailani alopecia wisp3 mutation vspgx probe desnities twist biosciences twist pac bio snvs prs polygenic risk score carrier screening oncogenic variants oncogenic oncgenic onco clinical ongenic varseq 2.5.0 ngs validation couple workflows small variants medelian disorders assays automation varseq cloud varseq browser ngs scalability cloud deployment enterprise genomics genomic research clinical labs on premise cpic cyp2d6 phase variants trio workflow complex variant long-read compound het compound variants oxford nanopore short read sequencing long read sequencing ce mark ivdr sickkids pcr tests viral infection sars-cov-2 covid19 covid-19 match gene lists count alleles phorank dbnsfp cosmic and civic omim gnomad clinical trials patient-linked data firewall medical records healthcare cyber security tumor-normal sentieon coverage statistics cram tso500 illumina family var copy number variant dragen software development science research pca goldenhelix clingen warehousing solutions single nucleotide variants variant anaysis clinvar dna analysis loss of function dr. robert hamilton