jordanlab / tagoreLinks
The script presents a simple way to visualize features on human chromosome ideograms
☆42Updated 5 months ago
Alternatives and similar repositories for tagore
Users that are interested in tagore are comparing it to the libraries listed below
Sorting:
- ☆44Updated last year
- Merging paired-end reads and removing adapters☆30Updated 5 years ago
- for visual evaluation of read support for structural variation☆55Updated last year
- What is true, thank you, ernestly. A large variant benchmarking tool analogous to hap.py for small variants.☆33Updated 2 years ago
- TIDDIT - structural variant calling☆76Updated 6 months ago
- ☆51Updated 6 years ago
- (WIP) best-practices workflow for rare disease☆62Updated last year
- Toolkit for the design and analysis of amplicon sequencing experiments utilizing unique molecular identifiers (UMIs)☆42Updated last month
- Suite of tools for analysing off-target reads to find CNVs, homozygous regions, and shared haplotypes☆31Updated 2 months ago
- Location of public benchmarking; primarily final results☆18Updated 7 months ago
- Structural Variation and fusion detection using targeted sequencing data from circulating cell free DNA☆29Updated last year
- Generic human DNA variant annotation pipeline☆58Updated last year
- Structural Variant Prediction Viewer☆35Updated 8 years ago
- POSTRE: Prediction Of STRuctural variant Effects☆28Updated 7 months ago
- Toolkit for genome-wide analysis of tandem repeats☆58Updated 2 weeks ago
- Filtering and profiling of next-generational sequencing data using region-specific rules☆25Updated 9 years ago
- Human reference genome analysis sets☆55Updated 2 years ago
- LongcallR is a SNP caller for single molecule long-read RNA-seq data☆67Updated last month
- Pipeline for de novo clustering of long transcriptomic reads☆26Updated 3 years ago
- ☆23Updated 4 months ago
- Structural variant VCF annotation, duplicate removal and comparison☆34Updated 7 months ago
- Allo: a multi-mapped read rescue strategy for gene regulatory analyses☆24Updated last year
- Phylogeny-based Contamination Detection in Mitochondrial and Whole-Genome Sequencing Studies☆18Updated 2 years ago
- Deep learning-based structural variant filtering method☆39Updated last year
- Structural variant (SV) analysis tools☆38Updated last year
- A tool for genotyping Variable Number Tandem Repeats (VNTR) from sequence data☆46Updated 10 months ago
- Structural variant merging tool☆55Updated last year
- An R package for estimating poly(A)-tail lengths in Oxford Nanopore RNA and DNA reads.☆54Updated 11 months ago
- Python scripts for matching output of Pacific Biosciences IsoSeq RNA-seq pipeline to an annotation file.☆23Updated 10 years ago
- mity: A highly sensitive mitochondrial variant analysis pipeline for whole genome sequencing data☆38Updated last month