Alternatives and similar repositories for snpedia-23andme:

Users that are interested in snpedia-23andme are comparing it to the libraries listed below

• arrogantrobot / 23andme2vcf
  convert your 23andme raw file to VCF | DEPRECATED, please see https://github.com/plantimals/2vcf
  ☆96Updated 5 years ago
• plantimals / 2vcf
  convert 23andme or Ancestry.com raw genotype calls into VCF format, with dbSNP annotations
  ☆54Updated 5 years ago
• mentatpsi / OSGenome
  An Open Source Web Application for Genetic Data (SNPs) using 23AndMe and Data Crawling Technologies
  ☆122Updated 11 months ago
• 23andMe / yhaplo
  Identifying Y-chromosome haplogroups in arbitrarily large samples of sequenced or genotyped men
  ☆108Updated 2 months ago
• cslarsen / arv
  A fast 23andMe DNA parser and inferrer for Python
  ☆117Updated 5 years ago
• 23andMe / seqseek
  Easy access to human reference genome sequences
  ☆56Updated last year
• madprime / genevieve
  Genevieve genome report tool
  ☆14Updated 2 years ago
• sequencing / isaac_aligner
  Isaac Genome Alignment Software
  ☆37Updated 9 years ago
• ekg / fastahack
  utilities for indexing and sequence extraction from FASTA files
  ☆59Updated 3 years ago
• apriha / snps
  tools for reading, writing, merging, and remapping SNPs
  ☆104Updated last week
• verilylifesciences / genomewarp
  GenomeWarp translates genetic variants from one genome assembly version to another.
  ☆97Updated last year
• vgteam / xg-old
  succinct labeled graphs with collections and paths
  ☆15Updated 6 years ago
• slowkow / pytabix
  Retrieve data in genomic intervals with a Python interface for tabix.
  ☆83Updated 7 years ago
• cjlee112 / pygr
  Python graph database framework for bioinformatics
  ☆93Updated 3 years ago
• UMCUGenetics / IAP
  Illumina analysis pipeline
  ☆14Updated 4 years ago
• BioInterchange / Ontologies
  Home of the Genomic Feature and Variation Ontology (GFVO)
  ☆16Updated 3 years ago
• apriha / lineage
  tools for genetic genealogy and the analysis of consumer DNA test results
  ☆166Updated last month
• ngopal / 23andMe
  python module to help explore raw data from 23andMe
  ☆48Updated 9 years ago
• hammerlab / cycledash
  Variant Caller Analysis Dashboard and Data Management System
  ☆36Updated 8 years ago
• microsoft / PhyloD
  A suite of machine learning tools for modeling viral adaptation to host immune responses.
  ☆12Updated last year
• GATB / bcalm
  compacted de Bruijn graph construction in low memory
  ☆99Updated 3 months ago
• yechengxi / DBG2OLC
  A genome assembler that reduces the computational time of human genome assembly from 400,000 CPU hours to 2,000 CPU hours, utilizing long…
  ☆66Updated 4 years ago
• SynBioDex / SBOL-specification
  The Synthetic Biology Open Language (SBOL)
  ☆15Updated last year
• marbl / MHAP
  MinHash Alignment Process (MHAP, pronounced MAP): locality-sensitive hashing to detect long-read overlaps and utilities
  ☆96Updated 2 years ago
• cwarden45 / DTC_Scripts
  Scripts to Analyze DTC Sequencing and Genotyping Data (and some comparisons to Veritas WGS data)
  ☆19Updated 2 months ago
• bioperl / bioperl.github.io
  The BioPerl Web site: http://bioperl.org
  ☆14Updated 5 years ago
• stevenliuyi / admix
  an admixture analysis tool for Python that supports raw data from 23andme, AncestryDNA, etc.
  ☆60Updated 2 years ago
• ncbi / ncbi-vdb
  ncbi-vdb
  ☆89Updated 2 weeks ago
• BioJulia / BioFmtSpecimens
  A collection of bioinformatics file format specimens to test against
  ☆47Updated 5 years ago
• opencb / biodata
  Java library that models biological entities and their equivalents in different file formats typically used in bioinformatics. Found a bu…
  ☆29Updated this week