MeHelmy / princessLinks
☆80Updated 4 months ago
Alternatives and similar repositories for princess
Users that are interested in princess are comparing it to the libraries listed below
Sorting:
- Code for phasing SVs with SNPs☆52Updated 5 years ago
- ☆48Updated last year
- Structural variant caller☆54Updated 3 years ago
- Variant annotation and merging pipeline☆36Updated last month
- Public Benchmark of Long-Read Structural Variant Caller on PacBio CCS HG002 Data☆51Updated 4 years ago
- Set of tools to manipulate and visualize modified base bam files☆56Updated 2 years ago
- SV genotyping with long reads☆39Updated 2 years ago
- Segmental Duplication Assembler (SDA).☆44Updated 2 years ago
- ☆76Updated 5 years ago
- ☆34Updated last year
- MarginPolish: Graph based assembly polishing☆46Updated 4 years ago
- Copy number variant caller and depth visualization utility for PacBio HiFi reads☆43Updated 8 months ago
- TGS scaffolding☆46Updated 3 years ago
- DEPRECATED - Workflow for the comprehensive detection and prioritization of variants in human genomes with PacBio HiFi reads☆38Updated last year
- Structural Variants Pipeline for Long Reads☆44Updated 6 years ago
- Error correction of ONT transcript reads☆58Updated last year
- A battery of methylation tools for PacBio HiFi reads☆36Updated last month
- An easy way to run BioNano genomic analysis☆27Updated 4 years ago
- Swipe your Structural Variants called on long (ONT/PacBio) reads with short exact (Illumina) reads.☆32Updated 2 years ago
- calling SVs from Blasr contig level alignments☆54Updated 7 years ago
- Reference-based variant calling pipeline for a pair of phased haplotype assemblies☆100Updated 4 years ago
- A Nextflow workflow to generate lift over files for any pair of genomes☆68Updated 3 weeks ago
- DNA methylation analysis downstream to Nanopolish for Oxford Nanopore DNA sequencing datasets☆28Updated 2 years ago
- Compute N50/NG50 and auN/auNG☆32Updated last year
- Genome scaffolding based on HiC data in heterozygous and high ploidy genomes☆60Updated 6 months ago
- DNA methylation analysis downstream to Nanopolish for Oxford Nanopore DNA sequencing datasets☆34Updated 4 years ago
- Pipeline for structural variant image curation and analysis.☆48Updated 3 years ago
- ☆31Updated 10 months ago
- finshingTool☆54Updated 8 years ago
- Efficient and accurate pathogenicity prediction for coding and regulatory structural variants in long-read genome sequencing☆36Updated last year