mgaleyuw / MeOWLinks
Automated Detection and Qualification of Differential Methylation
☆14Updated 2 years ago
Alternatives and similar repositories for MeOW
Users that are interested in MeOW are comparing it to the libraries listed below
Sorting:
- Methylmap is a tool for visualization of modified nucleotide frequencies for large cohort sizes.☆21Updated 9 months ago
- ☆26Updated 7 months ago
- Immuological gene typing and annotation for genome assembly☆38Updated 9 months ago
- add true-negative SVs from a population callset to a truth-set.☆15Updated 3 years ago
- Structural variant (SV) analysis tools☆39Updated last year
- SV analysis of the long-read sequencing data of the 1019 samples of the 1KG-ONT panel☆38Updated 7 months ago
- Easy genomic regions for short-read variant calling☆45Updated 3 months ago
- Structural variant VCF annotation, duplicate removal and comparison☆34Updated 2 months ago
- Location of public benchmarking; primarily final results☆18Updated 9 months ago
- modPhred is a pipeline for detection of DNA/RNA modifications from raw ONT data☆16Updated last year
- This tools counts the number of specific k-mers within sequence data. The counts can then be compare to other counts to determine to comp…☆30Updated last year
- ☆16Updated 10 months ago
- Structural variant merging tool☆57Updated last year
- Structural Variant Prediction Viewer☆35Updated 8 years ago
- ☆33Updated 3 years ago
- ☆24Updated 11 months ago
- Splice junction analysis and filtering from BAM files☆42Updated 3 years ago
- Pipeline for structural variant image curation and analysis.☆49Updated 4 years ago
- Suite of tools for analysing off-target reads to find CNVs, homozygous regions, and shared haplotypes☆31Updated 4 months ago
- a lexicographically-based GTF/GFF sorter☆35Updated 7 months ago
- Tools for merging Tandem Repeat VCF files☆37Updated 7 months ago
- perSVade: personalized Structural Variation detection☆40Updated 3 months ago
- Genotyping of segregating mobile elements insertions☆19Updated 4 years ago
- Functions to compare a SV call sets against a truth set.☆30Updated 5 months ago
- Detect and phase minor SNVs from long-read sequencing data☆14Updated 3 years ago
- ☆31Updated last year
- Alignment-free genotyper for SNPs and short indels, implemented in Python.☆52Updated 9 months ago
- Viola is a flexible and powerful python package designed specifically for analysis of genomic structural variant (SV) signatures.☆26Updated last year
- A tutorial on structural variant calling for short read sequencing data☆38Updated last year
- Efficient and accurate pathogenicity prediction for coding and regulatory structural variants in long-read genome sequencing☆39Updated 2 weeks ago