ncbi / ncbi-vdbLinks
ncbi-vdb
☆92Updated last week
Alternatives and similar repositories for ncbi-vdb
Users that are interested in ncbi-vdb are comparing it to the libraries listed below
Sorting:
- NGS Language Bindings☆120Updated 2 years ago
- ☆107Updated 3 weeks ago
- Scalable gVCF merging and joint variant calling for population sequencing projects☆174Updated last year
- Scripts, utilities and programs for genomic bioinformatics.☆83Updated last month
- GenomeWarp translates genetic variants from one genome assembly version to another.☆97Updated 2 years ago
- ☆63Updated 9 years ago
- Utilities for building and managing bioconda recipes☆103Updated last month
- Genotype and phase short tandem repeats using Illumina whole-genome sequencing data☆100Updated 2 years ago
- ☆36Updated 8 months ago
- Plugins for the Ensembl Variant Effect Predictor (VEP)☆163Updated 2 weeks ago
- A pipelining tool to automate and standardise bioinformatics analyses on cluster environments.☆98Updated 2 years ago
- Long read production pipelines☆151Updated 2 weeks ago
- Do not use - please refer to our newest code: https://github.com/cgat-developers/cgat-apps☆124Updated 7 years ago
- SRAToolkit has been REPLACED - see README☆37Updated 9 years ago
- small RNA analysis from NGS data☆37Updated last year
- Application for inferring subclonal composition and evolution from whole-genome sequencing data.☆113Updated 3 years ago
- Platypus Variant Caller☆108Updated last year
- Annotate models of genetic inheritance patterns in variant files (vcf files)☆84Updated 2 weeks ago
- dbVar☆40Updated 3 years ago
- python access to UCSC genomes database☆136Updated 5 years ago
- Annotation of VCF variants with functional impact and from databases (executable+library)☆63Updated last week
- TADbit is a complete Python library to deal with all steps to analyze, model and explore 3C-based data. With TADbit the user can map FAST…☆107Updated last month
- VarSim: A high-fidelity simulation validation framework for high-throughput genome sequencing with cancer applications☆90Updated last year
- Identification of differential RNA modifications from nanopore direct RNA sequencing☆160Updated last year
- ☆82Updated 7 years ago
- IGV Web App☆126Updated 2 weeks 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 this week
- a Medical Genetics Sequence Analysis Pipeline☆84Updated last week
- EDGE is a highly adaptable bioinformatics platform that allows laboratories to quickly analyze and interpret genomic sequence data.☆76Updated 2 weeks ago
- A modular annotation tool for genomic variants☆139Updated last week