DECIPHER-genomics / GenoverseLinks
HTML5 scrollable genome browser
☆111Updated last year
Alternatives and similar repositories for Genoverse
Users that are interested in Genoverse are comparing it to the libraries listed below
Sorting:
- Read visualizer for structural variants☆84Updated 7 years ago
- Annotation of VCF variants with functional impact and from databases (executable+library)☆62Updated this week
- NextSeq specific bcl2fastq2 wrapper.☆55Updated 4 years ago
- VarSim: A high-fidelity simulation validation framework for high-throughput genome sequencing with cancer applications☆90Updated 11 months ago
- An NGS read trimming tool that is specific, sensitive, and speedy. (production)☆122Updated 4 months ago
- ABRA2☆92Updated 2 years ago
- Very simple, pure python, BAM file reader☆79Updated 6 years ago
- ☆57Updated 5 years ago
- Documentation and description of AWS iGenomes S3 resource.☆116Updated 9 months ago
- Genomic Interactive Visualization Engine☆145Updated 2 years ago
- Annotate models of genetic inheritance patterns in variant files (vcf files)☆84Updated last month
- NEAT read simulation tools☆101Updated 3 years ago
- Biopieces is a bioinformatic framework of tools easily used and easily created.☆142Updated 7 years ago
- Platypus Variant Caller☆108Updated last year
- Lima - Demultiplex Barcoded PacBio Samples☆67Updated 4 months ago
- Mutation Identification Pipeline. Read the latest documentation:☆47Updated last year
- Browser based application for viewing bam alignments☆56Updated 8 years ago
- Detection of copy number changes in Germline/Trio/Somatic contexts in NGS data☆89Updated last week
- Simple FASTQ quality assessment using Python☆108Updated 4 years ago
- An efficient FASTQ manipulation suite☆138Updated 5 years ago
- ClassifyCNV: a tool for clinical annotation of copy-number variants☆67Updated 2 years ago
- Automatically exported from code.google.com/p/ea-utils☆96Updated 2 years ago
- ☆82Updated 3 years ago
- All source code of the crispor.org website☆79Updated 3 weeks ago
- LoFreq Star: Sensitive variant calling from sequencing data☆107Updated 3 years ago
- Annocript is a pipeline for the annotation of de-novo generated transcriptomes. It executes BLAST analysis with UniProt, NCBI Conserved …☆56Updated 5 years ago
- The DevNet project on github stores the PacBio DevNet website.☆116Updated 7 years ago
- Somatic and germline variant caller for amplicon data. Recommended caller for tumor-only workflows.☆98Updated 3 years ago
- Galaxy RNA workbench☆40Updated 4 years ago
- This repository contains information about latest release from Genome in a Bottle project☆75Updated 6 years ago