Alternatives and similar repositories for gedmatch-tools:

Users that are interested in gedmatch-tools are comparing it to the libraries listed below

• apriha / lineage
  tools for genetic genealogy and the analysis of consumer DNA test results
  ☆167Updated last month
• yulvil / chromosome-browser
  Visualize your DNA segments from gedmatch, ftdna, myheritage, 23andme
  ☆22Updated 4 years ago
• plashchynski / dna-raw-tools
  Tools to work with 23andMe and AncestryDNA raw files
  ☆11Updated 7 years ago
• jonathanbrecher / sharedclustering
  Tools to extract more information from DNA testing shared match lists
  ☆22Updated 2 years ago
• apriha / snps
  tools for reading, writing, merging, and remapping SNPs
  ☆108Updated last month
• 23andMe / yhaplo
  Identifying Y-chromosome haplogroups in arbitrarily large samples of sequenced or genotyped men
  ☆110Updated 2 months ago
• plantimals / 2vcf
  convert 23andme or Ancestry.com raw genotype calls into VCF format, with dbSNP annotations
  ☆56Updated 5 years ago
• jeftreece / dnamatch-tools
  open source tools providing capabilities for your DNA data from various DNA testing companies
  ☆43Updated last year
• 23andMe / api-example-flask
  An example Python app on 23andMe's genome API using the flask microframework.
  ☆71Updated last year
• DReichLab / AdmixTools
  Tools test whether admixture occurred and more
  ☆196Updated 7 months ago
• tkrahn / extract23
  Extract a simulated 23andMe (V3) style file from a Whole Genome BAM file
  ☆28Updated last month
• stevenliuyi / admix
  an admixture analysis tool for Python that supports raw data from 23andme, AncestryDNA, etc.
  ☆64Updated 2 years ago
• plashchynski / awesome-genetics
  A curated list of awesome personal genomics software, libraries, and educational resources.
  ☆134Updated last year
• Phelimb / BIGSI
  BItsliced Genomic Signature Index - Efficient indexing and search in very large collections of WGS data
  ☆126Updated last year
• nh13 / DWGSIM
  Whole Genome Simulator for Next-Generation Sequencing
  ☆96Updated 4 months ago
• 23andMe / seqseek
  Easy access to human reference genome sequences
  ☆56Updated 2 years ago
• Illumina / akt
  Ancestry and Kinship Tools
  ☆70Updated 2 years ago
• piratical / Madeline_2.0_PDE
  The Madeline 2.0 Pedigree Drawing Engine (PDE) is a pedigree drawing program designed to handle large and complex pedigrees with an empha…
  ☆20Updated last year
• counsyl / hgvs
  HGVS variant name parsing and generation
  ☆174Updated last year
• genometools / genometools
  GenomeTools genome analysis system.
  ☆307Updated last year
• chapmanb / cloudbiolinux
  CloudBioLinux: configure virtual (or real) machines with tools for biological analyses
  ☆257Updated last year
• ga4gh-beacon / specification
  GA4GH Beacon specification.
  ☆32Updated 2 years ago
• josiahseaman / FluentDNA
  FluentDNA allows you to browse sequence data of any size using a zooming visualization similar to Google Maps. You can use FluentDNA as …
  ☆65Updated 3 years ago
• ncbi / ncbi-vdb
  ncbi-vdb
  ☆91Updated this week
• arrogantrobot / 23andme2vcf
  convert your 23andme raw file to VCF | DEPRECATED, please see https://github.com/plantimals/2vcf
  ☆97Updated 5 years ago
• marbl / verkko
  Telomere-to-telomere assembly of accurate long reads (PacBio HiFi, Oxford Nanopore Duplex, HERRO corrected Oxford Nanopore Simplex) and O…
  ☆330Updated 2 weeks ago
• ga4gh / ga4gh-server
  Reference implementation of the APIs defined in ga4gh-schemas. RETIRED 2018-01-24
  ☆98Updated 7 years ago
• hall-lab / speedseq
  A flexible framework for rapid genome analysis and interpretation
  ☆316Updated 2 years ago
• nanoporetech / medaka
  Sequence correction provided by ONT Research
  ☆450Updated 6 months ago
• nanoporetech / pod5-file-format
  Pod5: a high performance file format for nanopore reads.
  ☆147Updated 5 months ago