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
- ☆57Updated 5 years ago
- Somatic and germline variant caller for amplicon data. Recommended caller for tumor-only workflows.☆98Updated 3 years ago
- An NGS read trimming tool that is specific, sensitive, and speedy. (production)☆122Updated 4 months ago
- Annotate models of genetic inheritance patterns in variant files (vcf files)☆82Updated 2 weeks ago
- Annotation of VCF variants with functional impact and from databases (executable+library)☆62Updated 2 weeks ago
- ☆95Updated 2 years ago
- Simple FASTQ quality assessment using Python☆109Updated 4 years ago
- Workflows used for WGS data processing -- replaced by https://github.com/gatk-workflows/gatk4-genome-processing-pipeline☆57Updated 5 years ago
- LoFreq Star: Sensitive variant calling from sequencing data☆107Updated 3 years ago
- This repository contains information about latest release from Genome in a Bottle project☆74Updated 6 years ago
- NextSeq specific bcl2fastq2 wrapper.☆55Updated 4 years ago
- Documentation and description of AWS iGenomes S3 resource.☆116Updated 8 months ago
- An efficient FASTQ manipulation suite☆138Updated 5 years ago
- Platypus Variant Caller☆108Updated last year
- Genomic Interactive Visualization Engine☆145Updated 2 years ago
- De novo transcriptome assembler for short reads☆63Updated 7 years ago
- ABRA2☆92Updated 2 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
- Very simple, pure python, BAM file reader☆79Updated 6 years ago
- ☆91Updated 3 years ago
- Detection of copy number changes in Germline/Trio/Somatic contexts in NGS data☆87Updated 2 months ago
- ☆123Updated last month
- ☆82Updated 3 years ago
- Lima - Demultiplex Barcoded PacBio Samples☆66Updated 3 months ago
- Visualization and annotation of CNVs from population-scale whole-genome sequencing data☆72Updated 7 years ago
- Dockerised Next Generation Sequencing Pipeline (QC, Align, Calling, Annotation)☆86Updated 8 years ago
- ClassifyCNV: a tool for clinical annotation of copy-number variants☆66Updated 2 years ago
- Detect germline or somatic variants from normal or tumour/normal whole-genome or targeted sequencing☆133Updated 5 years ago
- ☆82Updated 6 years ago