Illumina / GraphAlignmentViewerLinks
☆35Updated 3 years ago
Alternatives and similar repositories for GraphAlignmentViewer
Users that are interested in GraphAlignmentViewer are comparing it to the libraries listed below
Sorting:
- ☆42Updated 10 months ago
- Public Benchmark of Long-Read Structural Variant Caller on PacBio CCS HG002 Data☆51Updated 4 years ago
- ☆39Updated last year
- Tools for the analysis of structural variation in genomes☆80Updated last year
- TIDDIT - structural variant calling☆74Updated 3 months ago
- Runs a combination of tools to generate structural variant calls on whole-genome sequencing data☆48Updated 5 years ago
- Tool to annotate outfiles from ExpansionHunter and TRGT with the pathologic implications of the repeat☆32Updated 3 weeks ago
- What is true, thank you, ernestly. A large variant benchmarking tool analogous to hap.py for small variants.☆32Updated last year
- don't get DUP'ed or DEL'ed by your putative SVs.☆106Updated 4 years ago
- MetaSV: An accurate and integrative structural-variant caller for next generation sequencing☆56Updated 8 years ago
- Toolkit for genome-wide analysis of tandem repeats☆58Updated 4 months ago
- ☆51Updated 5 years ago
- A tool for genotyping Variable Number Tandem Repeats (VNTR) from sequence data☆44Updated 7 months ago
- A copy number caller for SMN1 and SMN2 to enable SMA diagnosis and carrier screening with WGS☆49Updated last year
- ☆21Updated 3 years ago
- Efficient and accurate pathogenicity prediction for coding and regulatory structural variants in long-read genome sequencing☆36Updated last year
- DEPRECATED - Workflow for the comprehensive detection and prioritization of variants in human genomes with PacBio HiFi reads☆38Updated last year
- Toolkit for calling structural variants using short or long reads☆107Updated last month
- heuristics to merge structural variant calls in VCF format.☆36Updated 8 years ago
- for visual evaluation of read support for structural variation☆54Updated last year
- A tool for visualizing alignments of reads in regions containing tandem repeats☆86Updated last year
- Methods to integrate data from multiple genome sequencing datasets and form consensus variant calls☆44Updated 3 years ago
- SMN1 copy-number and sequence variant analysis from next generation sequencing data☆23Updated 2 years ago
- Structural variant caller☆54Updated 3 years ago
- RetroSeq is a bioinformatics tool that searches for mobile element insertions from aligned reads in a BAM file and a library of reference…☆67Updated 2 years ago
- Data from the Human PanGenomics Project☆60Updated 4 years ago
- Methylation Phasing for Nanopore Sequencing☆48Updated 2 years ago
- python plotly Circos from VCF☆38Updated last year
- Set of tools to manipulate and visualize modified base bam files☆56Updated 2 years ago
- Robust detection of clinically relevant structural and copy number variation from whole genome sequencing data☆72Updated 10 months ago