9 skills found
chasewnelson / SNPGenieProgram for estimating πN/πS, dN/dS, and other diversity measures from next-generation sequencing data
biocore-ntnu / SnpflipReport reverse and ambiguous strand SNPs in GWAS data
automata-network / Amd Sev Snp Attestation SDKThe Automata AMD SEV-SNP Attestation SDK is a software development kit designed to help users generate the AMD SEV-SNP Attestation Report using Rust across different cloud service providers, and generate Risc0 and SP1 ZK Proofs which can be verified on-chain. Powered by Automata
VirtualPharmacist / VpVirtual Pharmacist is a web tool that interprets personal genome for the impact of genetic variation on drug response. It can take variants data (VCF format), microarray SNP genotyping data and high-throughput sequencing data as input, and report to the users how the variants in their personal genomes impact their drug response, including drug efficacy, dosage and toxicity.
xie186 / Snp2reportA tool to automatically generate genetic testing report in Word document.
zaczap / PathscanAn easy to use tool to identify pathogenic variants in genomic data; identifies variants listed as pathogenic in ClinVar that the ACMG recommendation implies should be incidental, reportable findings from VCFs, Complete Genomics variant files, and 23andMe SNP reports.
cran / GenABEL:exclamation: This is a read-only mirror of the CRAN R package repository. GenABEL — genome-wide SNP association analysis. Homepage: http://www.genabel.org, http://forum.genabel.org,<U+000a>http://genabel.r-forge.r-project.org/ Report bugs for this package: http://r-forge.r-project.org/tracker/?group_id=505
CDPHE-bioinformatics / Ncbi Cluster TrackerCreate standalone HTML reports for tracking SNP clusters within NCBI Pathogen Detection
schae234 / FinalReportToolsTools to Handle Illumina SNP Final Reports
