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
- Generic human DNA variant annotation pipeline☆59Updated last year
- Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer☆55Updated this week
- Genomic VCF to tab-separated values☆48Updated 2 years ago
- Interpretable prioritization of splice variants in diagnostic next-generation sequencing☆18Updated last year
- CLAMMS is a scalable tool for detecting common and rare copy number variants from whole-exome sequencing data.☆30Updated 4 years ago
- List of IARC bioinformatics pipelines and resources☆53Updated 3 weeks ago
- Preprocessing tools for unique molecular index (UMI) sequencing reads☆31Updated 2 years ago
- PathOS is a clinical application for filtering, analysing and reporting on NGS variants☆29Updated 4 years ago
- Thousand Variant Callers Project Repository☆74Updated 6 years ago
- Mapped QC analysis program☆44Updated 7 years ago
- mity: A highly sensitive mitochondrial variant analysis pipeline for whole genome sequencing data☆39Updated 2 months ago
- RUFUS k-mer based genomic variant detection☆54Updated 10 months ago
- SiNVICT: Ultra-Sensitive Detection of Single Nucleotide Variants and Indels in Circulating Tumour DNA☆27Updated 5 years ago
- ☆27Updated 11 months ago
- R package for inferring copy number from read depth☆32Updated 3 years ago
- Remove primer sequence from BAM alignments by soft-clipping☆31Updated 5 years ago
- Simplify snpEff annotations for interesting cases☆22Updated 6 years ago
- A Framework to call Structural Variants from NGS based datasets☆22Updated 7 years ago
- CheckQC inspects the content of an Illumina runfolder and determines if it passes a set of quality criteria☆28Updated 3 weeks ago
- Gene Fusion Visualiser☆51Updated 2 years ago
- Generic Interactive Variant Analysis browser☆29Updated 3 years ago
- A set of tools to annotate VCF files with expression and readcount data☆29Updated 8 months ago
- gnomAD browser pre-ASHG 2018☆33Updated 5 years ago
- QDNAseq package for Bioconductor☆53Updated last year
- Personal diploid genome creation and coordinate conversion