vpc-ccg / svict
Structural Variation and fusion detection using targeted sequencing data from circulating cell free DNA
☆25Updated 3 months ago
Related projects: ⓘ
- novoBreak: local assembly for breakpoint detection in cancer genomes☆26Updated 6 years ago
- Structural variant VCF annotation, duplicate removal and comparison☆26Updated 6 months ago
- Plot CNV data with a genome viewer in R☆15Updated 7 years ago
- Viola is a flexible and powerful python package designed specifically for analysis of genomic structural variant (SV) signatures.☆25Updated last month
- Suite of tools for analysing off-target reads to find CNVs, homozygous regions, and shared haplotypes☆27Updated 2 months ago
- Copy Number Variation Detection In Next-generation sequencing Gene panels was designed for small (single-exon) copy number variation (CNV…☆20Updated 4 years ago
- Location of public benchmarking; primarily final results☆18Updated 2 years ago
- Reproducibility workflow for Gigante et al., 2018: Using long-read sequencing to detect imprinted DNA methylation☆22Updated 5 years ago
- VisCap is an open flexible, software program targeted to clinical laboratories for inference and visualization of germline copy number va…☆22Updated 4 years ago
- Structural Variation breakpoint discovery via adaptive learning☆15Updated last year
- Integrative analysis of complex structural variants