Alternatives and similar repositories for arv

Users that are interested in arv are comparing it to the libraries listed below

• 23andMe / seqseek
  Easy access to human reference genome sequences
  ☆57Updated 2 years ago
• mentatpsi / OSGenome
  An Open Source Web Application for Genetic Data (SNPs) using 23AndMe and Data Crawling Technologies
  ☆131Updated last year
• zhaofengli / snappy
  Helps you browse through and interpret your genotype data
  ☆50Updated 2 years ago
• plantimals / 2vcf
  convert 23andme or Ancestry.com raw genotype calls into VCF format, with dbSNP annotations
  ☆59Updated 5 years ago
• superbobry / snpy
  A wrapper-library for reading openSNP data
  ☆49Updated 7 years ago
• heiner / snpedia-23andme
  Analyse a genome file from 23andMe using the data on snpedia.com
  ☆21Updated 8 years ago
• 23andMe / yhaplo
  Identifying Y-chromosome haplogroups in arbitrarily large samples of sequenced or genotyped men
  ☆111Updated 4 months ago
• gedankenstuecke / genotyping_23andme
  My raw genotyping data from 23andme
  ☆35Updated 6 years ago
• cslarsen / dna-traits
  A fast 23andMe genome text file parser, now superseded by arv
  ☆65Updated 7 years ago
• plashchynski / awesome-genetics
  A curated list of awesome personal genomics software, libraries, and educational resources.
  ☆136Updated last year
• arrogantrobot / 23andme2vcf
  convert your 23andme raw file to VCF | DEPRECATED, please see https://github.com/plantimals/2vcf
  ☆97Updated 5 years ago
• apriha / snps
  tools for reading, writing, merging, and remapping SNPs
  ☆108Updated 3 months ago
• StanfordBioinformatics / loom
  A tool for running bioinformatics workflows locally or in the cloud.
  ☆30Updated 5 years ago
• stevenliuyi / admix
  an admixture analysis tool for Python that supports raw data from 23andme, AncestryDNA, etc.
  ☆67Updated 2 years ago
• hammerlab / cycledash
  Variant Caller Analysis Dashboard and Data Management System
  ☆36Updated 9 years ago
• Novartis / yap
  High throughput, pain-free big data pipelines.
  ☆30Updated 8 years ago
• lgautier / fastq-and-furious
  Efficient handling of FASTQ files from Python
  ☆51Updated last month
• openSNP / snpr
  The sources of the openSNP website
  ☆177Updated last month
• IQTLabs / freqgen
  🎯 Generate DNA sequences with specified amino acid, codon, and k-mer frequencies
  ☆16Updated 2 years ago
• madprime / genevieve
  Genevieve genome report tool
  ☆14Updated 2 years ago
• apriha / lineage
  tools for genetic genealogy and the analysis of consumer DNA test results
  ☆169Updated 3 months ago
• AlexsLemonade / refinebio
  Refine.bio harmonizes petabytes of publicly available biological data into ready-to-use datasets for cancer researchers and AI/ML scienti…
  ☆132Updated 9 months ago
• lairdm / islandplot
  SVG based genome viewer written in javascript using D3
  ☆33Updated 9 years ago
• 23andMe / api-example-flask
  An example Python app on 23andMe's genome API using the flask microframework.
  ☆71Updated 2 years ago
• ubiome-opensource / microbiome-tools
  For tool creators to share their inventions that analyze, visualize, and make meaning of microbiome data.
  ☆66Updated 8 years ago
• mattmight / calculendar
  A command line tool that uses a Boolean calculus of calendars for computing availability (currently supports Google Calendar API)
  ☆25Updated 3 years ago
• alexpreynolds / sample
  Performs memory-efficient reservoir sampling on very large input files delimited by newlines
  ☆69Updated 5 years ago
• cwarden45 / DTC_Scripts
  Scripts to Analyze DTC Sequencing and Genotyping Data (and some comparisons to Veritas WGS data)
  ☆19Updated 7 months ago
• Edinburgh-Genome-Foundry / sequenticon
  Generate identicons for DNA sequences with Python
  ☆37Updated last month
• tkrahn / extract23
  Extract a simulated 23andMe (V3) style file from a Whole Genome BAM file
  ☆30Updated 3 months ago