ExpressionAnalysis / CNV_RadarLinks
CNV Rapid Aberration Detection And Reporting
☆12Updated 4 years ago
Alternatives and similar repositories for CNV_Radar
Users that are interested in CNV_Radar are comparing it to the libraries listed below
Sorting:
- A webtool for the clinical interpretation of CNVs in rare disease patients☆12Updated 3 years ago
- SiNVICT: Ultra-Sensitive Detection of Single Nucleotide Variants and Indels in Circulating Tumour DNA☆27Updated 4 years ago
- Fast, accurate and simple to use command line tool for variant detection in NGS data.☆12Updated 5 years ago
- Structural Variation and fusion detection using targeted sequencing data from circulating cell free DNA☆29Updated last year
- ☆24Updated 11 months ago
- Structural variant VCF annotation, duplicate removal and comparison☆33Updated 4 months ago
- novoBreak: local assembly for breakpoint detection in cancer genomes☆26Updated 7 years ago
- Suite of tools for analysing off-target reads to find CNVs, homozygous regions, and shared haplotypes☆29Updated last year
- VisCap is an open flexible, software program targeted to clinical laboratories for inference and visualization of germline copy number va…☆23Updated 5 years ago
- Validation runs using bcbio: germline, somatic, structural variant calling and RNA-seq analyses☆31Updated 3 years ago
- A set of tools to annotate VCF files with expression and readcount data☆29Updated 4 months ago
- filtering trio-based genetic variants in VCFs for clinical review☆21Updated 4 years ago
- POSTRE: Prediction Of STRuctural variant Effects☆27Updated 4 months ago
- Streamlined duo/trio analysis and pedigree haplotyping: from VCF to interactive HTML☆15Updated 8 months ago
- Structural Variant Prediction Viewer☆34Updated 7 years ago
- Somatic point mutation caller☆17Updated 9 years ago
- Simplify snpEff annotations for interesting cases☆22Updated 6 years ago
- Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer☆47Updated this week
- Automatically design multiplex PCR primer pairs for diverse templates☆28Updated last year
- wg-blimp: an end-to-end analysis pipeline for whole genome bisulfite sequencing data☆28Updated 2 years ago
- Full-spectrum copy number variation detection by high-throughput DNA sequencing☆37Updated 3 years ago
- curPrimers is a tool for trimming primer sequences from amplicon based NGS reads☆16Updated last month
- Tools to process LIANTI sequence data☆23Updated 6 years ago
- Python scripts for matching output of Pacific Biosciences IsoSeq RNA-seq pipeline to an annotation file.☆23Updated 9 years ago
- for visual evaluation of read support for structural variation☆54Updated last year
- Immuological gene typing and annotation for genome assembly☆37Updated 4 months ago
- A new tool to infer sex from massively parallel sequencing data.☆17Updated 2 months ago
- Calib clusters barcode tagged paired-end reads based on their barcode and sequence similarity.☆39Updated 2 years ago
- A Framework to call Structural Variants from NGS based datasets☆22Updated 7 years ago
- ☆14Updated 7 years ago