Alternatives and similar repositories for extract23:

Users that are interested in extract23 are comparing it to the libraries listed below

• apriha / snps
  tools for reading, writing, merging, and remapping SNPs
  ☆103Updated last month
• 23andMe / yhaplo
  Identifying Y-chromosome haplogroups in arbitrarily large samples of sequenced or genotyped men
  ☆108Updated last month
• arrogantrobot / 23andme2vcf
  convert your 23andme raw file to VCF | DEPRECATED, please see https://github.com/plantimals/2vcf
  ☆96Updated 5 years ago
• genid / Yleaf
  Yleaf software for human Y-chromosomal haplogroup inference from next generation sequencing data
  ☆24Updated 3 months ago
• stschiff / sequenceTools
  ☆43Updated last month
• plantimals / 2vcf
  convert 23andme or Ancestry.com raw genotype calls into VCF format, with dbSNP annotations
  ☆54Updated 5 years ago
• apriha / lineage
  tools for genetic genealogy and the analysis of consumer DNA test results
  ☆166Updated last month
• Illumina / akt
  Ancestry and Kinship Tools
  ☆70Updated 2 years ago
• 23andMe / seqseek
  Easy access to human reference genome sequences
  ☆56Updated last year
• konradjk / exac_browser
  Browser for ExAC consortium data
  ☆106Updated 2 years ago
• brentp / peddy
  genotype :: ped correspondence check, ancestry check, sex check. directly, quickly on VCF
  ☆136Updated 3 years ago
• DaehwanKimLab / tophat
  Spliced read mapper for RNA-Seq
  ☆92Updated last year
• The-Sequence-Ontology / SO-Ontologies
  Collect of SO Ontologies
  ☆96Updated 2 months ago
• DReichLab / EIG
  Eigen tools by Nick Patterson and Alkes Price lab
  ☆181Updated last year
• Ensembl / ensembl-vep
  The Ensembl Variant Effect Predictor predicts the functional effects of genomic variants
  ☆464Updated this week
• dariober / ASCIIGenome
  Text Only Genome Viewer!
  ☆209Updated 5 months ago
• dcjones / fastq-tools
  Small utilities for working with fastq sequence files.
  ☆115Updated 2 years ago
• dnanexus-rnd / GLnexus
  Scalable gVCF merging and joint variant calling for population sequencing projects
  ☆154Updated 9 months ago
• nh13 / DWGSIM
  Whole Genome Simulator for Next-Generation Sequencing
  ☆96Updated last month
• DReichLab / AdmixTools
  Tools test whether admixture occurred and more
  ☆183Updated 4 months ago
• ncbi / ngs
  NGS Language Bindings
  ☆118Updated last year
• Illumina / Nirvana
  The nimble & robust variant annotator
  ☆174Updated 8 months ago
• andyrimmer / Platypus
  Platypus Variant Caller
  ☆105Updated 6 months ago
• lh3 / fermikit
  De novo assembly based variant calling pipeline for Illumina short reads
  ☆108Updated 4 years ago
• teepean / BAM-Analysis-Kit
  ☆18Updated 2 years ago
• alastair-droop / fqtools
  An efficient FASTQ manipulation suite
  ☆138Updated 4 years ago
• hall-lab / svtools
  Tools for processing and analyzing structural variants.
  ☆150Updated 2 years ago
• brentp / cruzdb
  python access to UCSC genomes database
  ☆135Updated 4 years ago
• seppinho / haplogrep-cmd
  HaploGrep - mtDNA haplogroup classification. Supporting rCRS and RSRS.
  ☆74Updated last year
• bihealth / vcfpy
  Python 3 library with good support for both reading and writing VCF
  ☆100Updated 6 months ago