Illumina / REViewer
A tool for visualizing alignments of reads in regions containing tandem repeats
☆84Updated last year
Alternatives and similar repositories for REViewer:
Users that are interested in REViewer are comparing it to the libraries listed below
- Robust detection of clinically relevant structural and copy number variation from whole genome sequencing data☆68Updated 7 months ago
- Data and information about the Polaris study☆53Updated 5 years ago
- ☆21Updated 3 years ago
- ☆35Updated 3 years ago
- Wally: Visualization of aligned sequencing reads and contigs☆114Updated last week
- Structural Variant Index☆72Updated 4 months ago
- Stratification BED files from the Global Alliance for Genomics and Health (GA4GH) Benchmarking Team and the Genome in a Bottle Consortium…☆79Updated 2 years ago
- don't get DUP'ed or DEL'ed by your putative SVs.☆105Updated 4 years ago
- Tandem repeat genotyping and visualization from PacBio HiFi data☆113Updated last week
- Tools for the analysis of structural variation in genomes☆79Updated last year
- Somatic structural variant caller for long-read data☆65Updated 3 weeks ago
- Comprehensive TE insertion identification with WGS/WES data from multiple sequencing technics☆109Updated last week
- SV caller for nanopore data☆91Updated 4 years ago
- Read visualizer for structural variants☆83Updated 6 years ago
- Same species annotation lift over pipeline.☆97Updated last year
- ☆39Updated last year
- Runs a combination of tools to generate structural variant calls on whole-genome sequencing data☆47Updated 4 years ago
- Data from the Human PanGenomics Project☆60Updated 3 years ago
- Filtering and profiling of next-generational sequencing data using region-specific rules☆77Updated last year
- ☆79Updated last month
- ☆53Updated 2 years ago
- VerifyBamID2: A robust tool for DNA contamination estimation from sequence reads using ancestry-agnostic method.☆97Updated 11 months ago
- Comprehensive benchmark of structural variant callers☆46Updated 4 years ago
- Tool to annotate outfiles from ExpansionHunter and TRGT with the pathologic implications of the repeat☆32Updated last month
- Lima - Demultiplex Barcoded PacBio Samples☆66Updated 2 months ago
- DEPRECATED - Workflow for the comprehensive detection and prioritization of variants in human genomes with PacBio HiFi reads☆38Updated last year
- CNV screening and annotation tool☆25Updated 8 years ago
- A copy number caller for SMN1 and SMN2 to enable SMA diagnosis and carrier screening with WGS☆49Updated last year
- A tool for somatic structural variant calling using long reads☆128Updated 2 weeks ago
- ClassifyCNV: a tool for clinical annotation of copy-number variants☆62Updated last year