genepi / 23andme-toolsLinks
Convert 23andMe data to VCFs
☆10Updated 9 years ago
Alternatives and similar repositories for 23andme-tools
Users that are interested in 23andme-tools are comparing it to the libraries listed below
Sorting:
- DNA/RNA pattern matching algorithm☆21Updated 5 months ago
- Rails application for storing and parsing clinical exome VCF files. Gene annotations can be retrieved via Biomart integration from Ensemb…☆10Updated 8 years ago
- Generic pipeline system☆23Updated 7 years ago
- These scripts reformat a VCF into a SQLite database, with R☆15Updated 4 years ago
- Variant Annotation, Segregation and Exclusion for family or cohort based rare-disease sequencing studies.☆12Updated 3 years ago
- A fast and flexible program to annotate/interpret genetic variants in VCF/BCF file☆20Updated 5 years ago
- FUSE filesystem for the DNAnexus storage system☆14Updated this week
- Python library and scripts for retrieval and storage of genomics data in HDF5 format☆27Updated 6 years ago
- Workflow Description Language compiler for the DNAnexus platform☆42Updated 2 years ago
- The overall codebase developed and used by the Vertebrate Resequencing group at the Sanger Institute☆32Updated 4 years ago
- Annotation of VCF variants with functional impact and from databases (executable+library)☆64Updated 2 weeks ago
- Reference-free variant discovery in large eukaryotic genomes☆41Updated 4 years ago
- Load numpy arrays and HDF5 files from VCF (variant call format)☆31Updated 8 years ago
- Sparse Project VCF: evolution of VCF to encode population genotype matrices efficiently☆59Updated 2 years ago
- ☆63Updated 9 years ago
- GWAS Catalog Ontology and Curation Infrastructure☆26Updated last week
- ☆11Updated 2 years ago
- ☆36Updated 9 months ago
- Polygenic score calculation from VCF in Nim.☆15Updated 5 years ago
- This package scales the huge gnomAD files to a SQLite database, which is easy and fast to query. It extracts from a gnomAD vcf the minor …☆52Updated last month
- Command line tools for CMDB varaints browser☆23Updated last year
- De novo adapter prediction algorithm for small RNA sequencing data☆24Updated 8 years ago
- ncbi-vdb☆93Updated last week
- Find and visualize rearrangements in DNA sequences☆54Updated last month
- (WIP) best-practices workflow for rare disease☆62Updated last year
- Workflows used for processing whole genome sequence data + germline variant calling. This Repository has been archived, please visit the …☆28Updated 5 years ago
- Annotate models of genetic inheritance patterns in variant files (vcf files)☆85Updated 3 weeks ago
- Scalable gVCF merging and joint variant calling for population sequencing projects☆175Updated last year
- WDL and CWL compiler for the DNAnexus platform☆35Updated last month
- Efficiently read and write sequencing data from Python☆69Updated 3 months ago