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
- ☆26Updated last year
- novoBreak: local assembly for breakpoint detection in cancer genomes☆25Updated 7 years ago
- A set of tools to annotate VCF files with expression and readcount data☆29Updated 7 months ago
- Abismal is a mapper of FASTQ bisulfite-converted short reads (between 50 and 1000 bases) to a FASTA reference genome.☆19Updated 2 weeks ago
- Long read to rMATS☆32Updated 2 years ago
- Automated human exome/genome variants detection from FASTQ files☆23Updated 4 years ago
- wg-blimp: an end-to-end analysis pipeline for whole genome bisulfite sequencing data☆28Updated 3 years ago
- CADD-SV – a framework to score the effect of structural variants☆16Updated 7 months ago
- Suite of tools for analysing off-target reads to find CNVs, homozygous regions, and shared haplotypes☆31Updated 2 months ago
- Identifying differentially methylated regions from MethylC-seq (bisulfite-sequencing) data☆28Updated 2 years ago
- Workflow for Sequenza, cellularity and ploidy☆22Updated 2 months ago
- Python scripts for matching output of Pacific Biosciences IsoSeq RNA-seq pipeline to an annotation file.☆23Updated 10 years ago
- Structural Variation and fusion detection using targeted sequencing data from circulating cell free DNA☆29Updated last year
- SiNVICT: Ultra-Sensitive Detection of Single Nucleotide Variants and Indels in Circulating Tumour DNA☆27Updated 5 years ago
- R API for browsing, analyzing, and manipulating reference-aligned genome graphs in a GenomicRanges framework☆41Updated last month
- ☆15Updated 7 years ago
- Structural variant VCF annotation, duplicate removal and comparison☆34Updated last week
- VisCap is an open flexible, software program targeted to clinical laboratories for inference and visualization of germline copy number va…☆22Updated 5 years ago
- for visual evaluation of read support for structural variation☆55Updated last year
- All-FIT - Allele-Frequency-based Imputation of Tumor Purity☆18Updated 6 years ago
- a Shiny/R application to view and annotate copy number variations☆28Updated 2 years ago
- Microsatellite instability (MSI) detection for cfDNA samples.☆19Updated 4 years ago
- Filters for false-positive mutation calls in NGS☆34Updated 6 years ago
- Polyidus provides a framework to catch chimeric DNA sequences with a tale of python☆10Updated 2 years ago
- Tools to process LIANTI sequence data☆23Updated 6 years ago
- Splice junction analysis and filtering from BAM files☆42Updated 3 years ago
- Fast, accurate and simple to use command line tool for variant detection in NGS data.☆12Updated 6 years ago
- Somatic point mutation caller☆17Updated 9 years ago
- alternative splicing analysis pipeline☆20Updated 4 years ago