23andMe / seqseekLinks
Easy access to human reference genome sequences
☆57Updated 2 years ago
Alternatives and similar repositories for seqseek
Users that are interested in seqseek are comparing it to the libraries listed below
Sorting:
- Identifying Y-chromosome haplogroups in arbitrarily large samples of sequenced or genotyped men☆111Updated 3 weeks ago
- convert your 23andme raw file to VCF | DEPRECATED, please see https://github.com/plantimals/2vcf☆98Updated 6 years ago
- Software pipeline for the analysis of CRISPR-Cas9 genome editing outcomes from sequencing data☆135Updated 6 years ago
- ncbi-vdb☆92Updated this week
- python access to UCSC genomes database☆136Updated 5 years ago
- tools for reading, writing, merging, and remapping SNPs☆109Updated 5 months ago
- an admixture analysis tool for Python that supports raw data from 23andme, AncestryDNA, etc.☆68Updated 3 years ago
- ☆62Updated 8 years ago
- Note: tabix and bgzip binaries are now part of the HTSlib project.☆91Updated 4 years ago
- Genome-wide imputation pipeline☆31Updated last year
- Browser for ExAC consortium data☆106Updated 3 years ago
- GenomeWarp translates genetic variants from one genome assembly version to another.☆97Updated 2 years ago
- Library for manipulating genomic variants and predicting their effects☆85Updated last year
- Workflow Description Language compiler for the DNAnexus platform☆42Updated 2 years ago
- A Variant Call Format reader for Python.☆76Updated 10 years ago
- Efficient handling of FASTQ files from Python☆51Updated last month
- A pipelining tool to automate and standardise bioinformatics analyses on cluster environments.☆97Updated 2 years ago
- NGS Language Bindings☆119Updated last year
- EDGE is a highly adaptable bioinformatics platform that allows laboratories to quickly analyze and interpret genomic sequence data.☆75Updated last week
- convert 23andme or Ancestry.com raw genotype calls into VCF format, with dbSNP annotations☆58Updated 5 years ago
- Reference implementation of the APIs defined in ga4gh-schemas. RETIRED 2018-01-24☆98Updated 7 years ago
- Ancestry and Kinship Tools☆70Updated 2 years ago
- Do not use - please refer to our newest code: https://github.com/cgat-developers/cgat-apps☆124Updated 6 years ago
- CloudBioLinux: configure virtual (or real) machines with tools for biological analyses☆257Updated last year
- utilities for indexing and sequence extraction from FASTA files☆59Updated 4 years ago
- Scripts, utilities and programs for genomic bioinformatics.☆83Updated 2 months ago
- ☆37Updated 4 months ago
- fast, memory-efficient, pythonic (and command-line) access to fasta sequence files☆88Updated 7 years ago
- Canvas - Copy number variant (CNV) calling from DNA sequencing data☆128Updated 5 years ago
- Retrieve data in genomic intervals with a Python interface for tabix.☆82Updated 8 years ago