23andMe / seqseek
Easy access to human reference genome sequences
☆56Updated last year
Related projects ⓘ
Alternatives and complementary repositories for seqseek
- convert your 23andme raw file to VCF | DEPRECATED, please see https://github.com/plantimals/2vcf☆96Updated 5 years ago
- NGS Language Bindings☆117Updated 11 months ago
- convert 23andme or Ancestry.com raw genotype calls into VCF format, with dbSNP annotations☆52Updated 5 years ago
- A fast Python library for VCF files leveraging Cython for speed.☆52Updated 6 years ago
- tools for reading, writing, merging, and remapping SNPs☆100Updated 2 months ago
- an admixture analysis tool for Python that supports raw data from 23andme, AncestryDNA, etc.☆57Updated 2 years ago
- ☆61Updated 8 years ago
- Workflow Description Language compiler for the DNAnexus platform☆40Updated last year
- Identifying Y-chromosome haplogroups in arbitrarily large samples of sequenced or genotyped men☆106Updated 2 weeks ago
- conda recipes for genomic data☆85Updated 3 years ago
- GenomeWarp translates genetic variants from one genome assembly version to another.☆97Updated last year
- genotype :: ped correspondence check, ancestry check, sex check. directly, quickly on VCF☆134Updated 3 years ago
- Reference implementation of the APIs defined in ga4gh-schemas. RETIRED 2018-01-24☆96Updated 6 years ago
- A pipelining tool to automate and standardise bioinformatics analyses on cluster environments.☆97Updated last year
- ncbi-vdb☆89Updated this week
- Browser for ExAC consortium data☆106Updated 2 years ago
- A Variant Call Format reader for Python.☆76Updated 9 years ago
- Software pipeline for the analysis of CRISPR-Cas9 genome editing outcomes from sequencing data☆133Updated 5 years ago
- python access to UCSC genomes database☆135Updated 4 years ago
- ☆35Updated last year
- A tool to genotype CYP2D6 with WGS data☆49Updated last year
- VCF-kit: Assorted utilities for the variant call format☆123Updated 3 months ago
- Efficient handling of FASTQ files from Python☆50Updated 2 months ago
- software tool for the manipulation, annotation, selection, and analysis of variants in the context of next-gen sequencing analysis☆31Updated 2 years ago
- Do not use - please refer to our newest code: https://github.com/cgat-developers/cgat-apps☆124Updated 6 years ago
- Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genes☆58Updated last week
- Python graph database framework for bioinformatics☆92Updated 2 years ago
- Retrieve data in genomic intervals with a Python interface for tabix.☆83Updated 7 years ago
- Infectious Disease Sequencing Platform☆79Updated 3 weeks ago
- Server wrapper that turns command line tools into web services☆60Updated 6 years ago