vpc-ccg / sedef
Identification of segmental duplications in the genome
☆27Updated 3 years ago
Alternatives and similar repositories for sedef:
Users that are interested in sedef are comparing it to the libraries listed below
- A module for improving the insertion sequences of structural variant calls☆30Updated 3 years ago
- An algorithm for centromere assembly using long error-prone reads☆26Updated 3 years ago
- use variant nesting information to flter overlapping sites from vg deconstruct output☆26Updated 9 months ago
- Improved Phased Assembler☆28Updated 3 years ago
- Tool for assessing/improving assembly quality in extra-long tandem repeats☆46Updated 4 years ago
- R package and wrapper functions for identifying serial structural variations from genome assemblies☆29Updated 6 months ago
- ☆30Updated 5 years ago
- building a human pangenome from the HPRCy1v2 genbank accessioned assemblies☆14Updated 2 years ago
- Method to optimally select samples for validation and resequencing☆27Updated 4 years ago
- CAMSA: a tool for Comparative Analysis and Merging of Scaffold Assemblies☆24Updated 5 years ago
- ☆42Updated 11 months ago
- ☆35Updated last year
- SV calling for diploid assemblies☆26Updated last year
- Exact Tandem Repeat Finder (not a TRF replacement)☆48Updated 5 years ago
- SV genotyping with long reads☆40Updated last year
- Convert HAL to VG☆22Updated 8 months ago
- Code for phasing SVs with SNPs☆52Updated 5 years ago
- ☆16Updated 11 months ago
- Convert RepeatMasker ".out" file into a gff3 with colors!!!☆21Updated 4 years ago
- Lightweight mosaic/somatic SV caller for long reads (WIP)☆28Updated 4 months ago
- SV genotyper for long reads with a variation graph☆12Updated 3 weeks ago
- Segmental Duplication Assembler (SDA).☆44Updated last year
- Tool for decomposition centromeric assemblies and long reads into monomers☆36Updated 2 years ago
- A tool for the recovery of unassembled telomeres from soft-clipped read alignments.☆35Updated this week
- Pipeline to detect PAVs (presence/absence variations) in genome comparison using whole genome alignment.☆29Updated 7 years ago
- Integrate multiple genome assemblies into a pangenome graph☆34Updated 2 years ago
- TideHunter: efficient and sensitive tandem repeat detection from noisy long reads using seed-and-chain☆20Updated 9 months ago
- Variant annotation and merging pipeline☆33Updated 2 weeks ago
- ☆17Updated last month
- Segmental duplication detection tool☆15Updated 2 years ago