✂️ ⚡ Rapid haploid variant calling and core genome alignment
snps 开源项目推荐(179 个)
snps 话题在 GitHub 上没有填写简介,这里按 Star 数汇总最相关的热门仓库。
热门项目 前 20
按 Star 数排序展示前 20 个 · GitHub 共 179 个仓库Strelka2 germline and somatic small variant caller
Convert SNPs in VCF format to PHYLIP, NEXUS, binary NEXUS, or FASTA alignments for phylogenetic analysis
个性化基因组学与蛋白质组学。主食:Ensembl,配菜:SNP
用于分析和探索遗传关系的工具
An Open Source Web Application for Genetic Data (SNPs) using 23AndMe and Data Crawling Technologies
A fast 23andMe DNA parser and inferrer for Python
tools for reading, writing, generating, merging, and remapping SNPs
Find causal cell-types underlying complex trait genetics
A fast 23andMe genome text file parser, now superseded by arv
Wrapper to a number of SNP web APIs
Population Genetics in Julia
Compressed storage for SNP data
Pan-genomic sequence analysis
Datastructures and algorithms for working with genetic variation
A tool for simulating random mutations in any genome
Estimate local SNP heritability and genetic covariance from GWAS summary association statistics.
An R package for fast and efficient visualizing of GWAS results using Q-Q and Manhattan plots directly from PLINK output files.
An Efficient Swiss Army Knife for Population Genomic Analyses in R
A haplotype analysis toolkit for natural variation study.
关于这个话题
- 清单取自 GitHub 话题页并按 Star 数排序,每次展示前 20 个项目;原始页面见 https://github.com/topics/snps。
- 该话题在 GitHub 上共有 179 个仓库, 本站收录的是其中最热门的 20 个,不是全量列表。
- Star / Fork 每日自动刷新一次,实时数据以 GitHub 为准。
- 当前 20 个项目累计 2844 Star,覆盖 6 种主要语言,数据更新于 2026-11-07。
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