ccmbioinfo / crg2Links
Research pipeline for exploring clinically relevant genomic variants
☆16Updated last week
Alternatives and similar repositories for crg2
Users that are interested in crg2 are comparing it to the libraries listed below
Sorting:
- Genomes on the Cloud, Mapping & Variant Calling Pipelines☆33Updated 8 years ago
- Automated next generation DNA sequencing analysis pipeline suited for clinical tests, with >99.9% sensitivity to Sanger sequencing at rea…☆26Updated 5 years ago
- List of IARC bioinformatics pipelines and resources☆53Updated this week
- Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer☆54Updated 2 weeks ago
- Generic human DNA variant annotation pipeline☆58Updated last year
- Interpretable prioritization of splice variants in diagnostic next-generation sequencing☆18Updated last year
- Preprocessing tools for unique molecular index (UMI) sequencing reads☆31Updated 2 years ago
- Simplify snpEff annotations for interesting cases☆22Updated 6 years ago
- Thousand Variant Callers Project Repository☆73Updated 6 years ago
- RUFUS k-mer based genomic variant detection☆54Updated 9 months ago
- gnomAD browser pre-ASHG 2018☆33Updated 4 years ago
- Genomic VCF to tab-separated values☆47Updated 2 years ago
- VVP (VAAST Variant Prioritizer) rapidly prioritizes genetic variants☆19Updated 7 years ago
- CLAMMS is a scalable tool for detecting common and rare copy number variants from whole-exome sequencing data.☆30Updated 4 years ago
- PathOS is a clinical application for filtering, analysing and reporting on NGS variants☆29Updated 4 years ago
- Call regions of homozygosity and make tentative UPD calls☆12Updated 4 months ago
- VCF-Miner: A graphical user interface for sorting, filtering and querying annotated VCF Files☆37Updated 5 years ago
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆29Updated 4 months ago
- SiNVICT: Ultra-Sensitive Detection of Single Nucleotide Variants and Indels in Circulating Tumour DNA☆27Updated 5 years ago
- Merging, Annotation, Validation, and Illustration of Structural variants☆75Updated 2 years ago
- Gene Fusion Visualiser☆51Updated 2 years ago
- Bamgineer: Introduction of simulated allele-specific copy number variants into exome and targeted sequence data sets☆37Updated 5 years ago
- Script to convert GTC/BPM files to VCF☆47Updated 2 weeks ago
- RetroSeq is a bioinformatics tool that searches for mobile element insertions from aligned reads in a BAM file and a library of reference…☆67Updated 2 years ago
- Mapped QC analysis program☆44Updated 7 years ago
- R package designed to simplify structural variant analysis☆73Updated 3 years ago
- Annotate models of genetic inheritance patterns in variant files (vcf files)☆84Updated 2 months ago
- Generic Interactive Variant Analysis browser☆29Updated 3 years ago
- 📊Evaluating, filtering, comparing, and visualising VCF☆28Updated 2 years ago
- (WIP) best-practices workflow for rare disease☆62Updated last year