dasmoth / dallianceLinks
Interactive web-based genome browser.
☆228Updated 6 years ago
Alternatives and similar repositories for dalliance
Users that are interested in dalliance are comparing it to the libraries listed below
Sorting:
- HGVS variant name parsing and generation☆176Updated 2 years ago
- Browser for ExAC consortium data☆106Updated 4 years ago
- HTML5 scrollable genome browser☆111Updated 2 years ago
- A tool set for short variant discovery in genetic sequence data.☆204Updated 4 years ago
- A powerful toolset for genome arithmetic.☆142Updated 4 years ago
- miscellaneous scripts for bioinformatics/genomics that dont merit their own repo.☆182Updated 7 years ago
- Dockerised Next Generation Sequencing Pipeline (QC, Align, Calling, Annotation)☆86Updated 8 years ago
- Reference implementation of the APIs defined in ga4gh-schemas. RETIRED 2018-01-24☆99Updated 8 years ago
- This repo provides tools to convert ClinVar data into a tab-delimited flat file, and also provides that resulting tab-delimited flat file…☆128Updated 5 years ago
- Extension for Jupyter which integrates igv.js☆154Updated 3 years ago
- Biopieces is a bioinformatic framework of tools easily used and easily created.☆144Updated 7 years ago
- A Javascript/d3 embeddable plugin for interactively visualizing statistical genetic data from customizable sources.☆163Updated 8 months ago
- BEDOPS: high-performance genomic feature operations☆357Updated 9 months ago
- A genotype query interface.☆136Updated 4 years ago
- Text Only Genome Viewer!☆231Updated last week
- C++ Library to parse Illumina InterOp files☆80Updated last month
- Documentation and description of AWS iGenomes S3 resource.☆120Updated last year
- a toolkit for working with Oxford nanopore data☆243Updated 2 years ago
- De novo assembly based variant calling pipeline for Illumina short reads☆110Updated 5 years ago
- web-based analysis tool for rare disease genomics☆199Updated last week
- List of gene lists for genomic analyses.☆224Updated 3 years ago
- Detect germline or somatic variants from normal or tumour/normal whole-genome or targeted sequencing☆133Updated 6 years ago
- A pipelining tool to automate and standardise bioinformatics analyses on cluster environments.☆98Updated 2 years ago
- Microassembly based somatic variant caller for NGS data☆154Updated 3 years ago
- de novo sequence assembler using string graphs☆243Updated 6 years ago
- NGS Language Bindings☆120Updated 2 years ago
- Library for manipulating genomic variants and predicting their effects☆85Updated last year
- GFF and GVF specification documents☆219Updated last year
- samblaster: a tool to mark duplicates and extract discordant and split reads from sam files.☆237Updated 4 years ago
- A 3'-end adapter contaminant trimmer☆95Updated 8 years ago