web-based protein structure viewer and analysis tool interactively or in batch mode
Private, local-first health intelligence for labs, 51 curated SNPs, wearables, light exposure, Biology Scores, optional AI, encrypted sync, sharing, and Agent Access.
R package: parallel computing toolset for relatedness and principal component analysis of SNP data (Development version only)
gwasrapidd: an R package to query, download and wrangle GWAS Catalog data
longcallR is a tool for SNP calling, haplotype phasing, and allele-specific analysis with long-read RNA-seq data.
Data management of large-scale whole-genome sequence variant calls using GDS files (Development version only)
A fast terminal-based viewer and command-line toolkit for molecular sequences (DNA, AA). View, translate, convert (to FASTA), and combine sequences aligned or not — all from the terminal.
A tool for simulating random mutations in any genome
SNPbinner is a utility for the generation of genotype crossover points and binmaps based on SNP data across recombinant inbred lines.
S&P 500 stock price prediction using Transformer model
Lightweight single-html-file-based Genome Segments playground for Visualize genome features cluster(gene arrow map or other features), add synteny among genome fragments or add crosslink among features, add short(PE/MP)/long reads(pacbio or nanopore) mapping or snpindel in vcf(not support complex sv yet), support all CIGAR of sam alignment, dire…
R package – HLA Genotype Imputation with Attribute Bagging (development version only)
R package for pedigree inference based on SNP data
vSNP -- validate SNPs
Towards a universal foundation model for biobank-scale human genome variation
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