hmgu-itg / VCF-liftoverLinks
Liftover VCF files
☆18Updated 8 years ago
Alternatives and similar repositories for VCF-liftover
Users that are interested in VCF-liftover are comparing it to the libraries listed below
Sorting:
- ☆35Updated 4 years ago
- ☆24Updated 11 months ago
- Immuological gene typing and annotation for genome assembly☆38Updated 7 months ago
- Pipeline for structural variation detection in cohorts☆52Updated 4 years ago
- Validation runs using bcbio: germline, somatic, structural variant calling and RNA-seq analyses☆31Updated 3 years ago
- Structural Variant Prediction Viewer☆35Updated 8 years ago
- novoBreak: local assembly for breakpoint detection in cancer genomes☆25Updated 7 years ago
- ☆23Updated 10 months ago
- Multi-sample genome coverage viewer to observe large, coverage-based anomalies alongside annotations and sample metadata☆58Updated 3 years ago
- Suite of tools for analysing off-target reads to find CNVs, homozygous regions, and shared haplotypes☆31Updated 2 months ago
- Fast and scalable variant annotation tool☆30Updated 3 years ago
- Evaluation of phasing performance☆23Updated 7 years ago
- heuristics to merge structural variant calls in VCF format.☆38Updated 9 years ago
- Plot CNV data with a genome viewer in R☆15Updated 8 years ago
- Bamgineer: Introduction of simulated allele-specific copy number variants into exome and targeted sequence data sets☆37Updated 5 years ago
- Benchmark pipeline for Structural Variation analyses, funded by the ALLBio.☆24Updated 11 years ago
- A tool for evaluating RNA seq mapping☆22Updated 6 years ago
- Pipeline for structural variant image curation and analysis.☆48Updated 3 years ago
- Structural variant VCF annotation, duplicate removal and comparison☆34Updated 2 weeks ago
- ☆51Updated 6 years ago
- Splice junction analysis and filtering from BAM files☆42Updated 3 years ago
- R API for browsing, analyzing, and manipulating reference-aligned genome graphs in a GenomicRanges framework☆41Updated last month
- Toolkit for genome-wide analysis of tandem repeats☆58Updated last month
- Enabling differential allele-specific analysis☆11Updated 10 months ago
- A method to identify structural variation from sequencing data in target regions☆32Updated 5 years ago
- Tools for processing and analyzing structural variants.☆33Updated 10 years ago
- Tools for merging Tandem Repeat VCF files☆36Updated 6 months ago
- ☆25Updated 7 years ago
- Mapped QC analysis program☆44Updated 7 years ago
- Automated human exome/genome variants detection from FASTQ files☆23Updated 4 years ago