WGSExtract / WGSExtract-Dev
WGS Extract Developers Repository
☆21Updated 5 months ago
Related projects: ⓘ
- tools for reading, writing, merging, and remapping SNPs☆97Updated 3 weeks ago
- convert 23andme or Ancestry.com raw genotype calls into VCF format, with dbSNP annotations☆50Updated 5 years ago
- A curated list of awesome personal genomics software, libraries, and educational resources.☆118Updated 6 months ago
- Extract a simulated 23andMe (V3) style file from a Whole Genome BAM file☆28Updated 7 years ago
- Identifying Y-chromosome haplogroups in arbitrarily large samples of sequenced or genotyped men☆104Updated last month
- Easy access to human reference genome sequences☆56Updated last year
- An Open Source Web Application for Genetic Data (SNPs) using 23AndMe and Data Crawling Technologies☆115Updated 7 months ago
- An Open Source Web Application for Genetic Data (SNPs) Data Crawling☆15Updated last year
- WGS Extract WWW home☆31Updated last month
- tools for genetic genealogy and the analysis of consumer DNA test results☆155Updated 2 months ago
- GenomeWarp translates genetic variants from one genome assembly version to another.☆97Updated last year
- This is the official development repository for BCFtools. See installation instructions and other documentation here http://samtools.gith…☆652Updated this week
- Genomics Extension for SQLite☆161Updated 2 weeks ago
- Assemble large genomes using short reads☆308Updated last week
- dbSNP☆121Updated 3 months ago
- A set of tools written in Perl and C++ for working with VCF files, such as those generated by the 1000 Genomes Project.☆497Updated 10 months ago
- Software pipeline for the analysis of CRISPR-Cas9 genome editing outcomes from sequencing data☆131Updated 5 years ago
- Utilities for building and managing bioconda recipes☆96Updated 3 weeks ago
- Analyse a genome file from 23andMe using the data on snpedia.com☆21Updated 7 years ago
- NGS Language Bindings☆118Updated 9 months ago
- The Ensembl Variant Effect Predictor predicts the functional effects of genomic variants☆445Updated 2 weeks ago
- Short-read sequencing tools☆147Updated this week
- IGV Web App☆114Updated 2 weeks ago
- GenomeTools genome analysis system.☆291Updated 7 months ago
- diploid SNV caller for error-prone reads☆177Updated 4 months ago
- A gap-closing software tool that uses long reads to enhance genome assembly.☆170Updated 2 weeks ago
- Helps you browse through and interpret your genotype data☆48Updated last year
- Telomere-to-telomere assembly of accurate long reads (PacBio HiFi, Oxford Nanopore Duplex, HERRO corrected Oxford Nanopore Simplex) and O…☆283Updated this week
- CloudBioLinux: configure virtual (or real) machines with tools for biological analyses☆257Updated 9 months ago