YingZhou001 / ImmuannotLinks
Immuological gene typing and annotation for genome assembly
☆38Updated 6 months ago
Alternatives and similar repositories for Immuannot
Users that are interested in Immuannot are comparing it to the libraries listed below
Sorting:
- Long-read splice alignment with high accuracy☆63Updated last year
- ☆23Updated 9 months ago
- Structural variant VCF annotation, duplicate removal and comparison☆34Updated 7 months ago
- Structural variant (SV) analysis tools☆38Updated last year
- Scripts and files used in the generation of the COLO829 somatic SV truthset.☆13Updated 3 years ago
- Easy genomic regions for short-read variant calling☆44Updated 3 weeks ago
- Automated Detection and Qualification of Differential Methylation☆14Updated last year
- ☆24Updated 5 months ago
- Structural variant merging tool☆55Updated last year
- PopSTR - A Population based microsatellite genotyper☆33Updated last year
- R API for browsing, analyzing, and manipulating reference-aligned genome graphs in a GenomicRanges framework☆41Updated 2 weeks ago
- Multi-sample genome coverage viewer to observe large, coverage-based anomalies alongside annotations and sample metadata☆58Updated 3 years ago
- Reproducibility workflow for Gigante et al., 2018: Using long-read sequencing to detect imprinted DNA methylation☆23Updated 6 years ago
- heuristics to merge structural variant calls in VCF format.☆38Updated 9 years ago
- ☆20Updated 3 years ago
- Tools for merging Tandem Repeat VCF files☆34Updated 5 months ago
- Location of public benchmarking; primarily final results☆18Updated 7 months ago
- Suite of tools for analysing off-target reads to find CNVs, homozygous regions, and shared haplotypes☆31Updated last month
- ☆33Updated 2 years ago
- Tumour-only somatic mutation calling using long reads☆27Updated 11 months ago
- ☆23Updated 4 months ago
- MethPhaser: methylation-based haplotype phasing of human genomes☆49Updated 7 months ago
- Functions to compare a SV call sets against a truth set.☆30Updated 3 months ago
- novoBreak: local assembly for breakpoint detection in cancer genomes☆25Updated 7 years ago
- Sample Contamination Estimate from VCF☆21Updated 11 months ago
- Splice junction analysis and filtering from BAM files☆42Updated 3 years ago
- Pipeline for structural variant image curation and analysis.☆48Updated 3 years ago
- Population-wide Deletion Calling☆35Updated 5 months ago
- Genotyping of segregating mobile elements insertions☆19Updated 4 years ago
- Pipeline for structural variation detection in cohorts☆51Updated 4 years ago