ggonnella / gfaviz
Graphical interactive tool for the visualization of sequence graphs in GFA format.
☆69Updated 6 years ago
Alternatives and similar repositories for gfaviz:
Users that are interested in gfaviz are comparing it to the libraries listed below
- Tool for assessing/improving assembly quality in extra-long tandem repeats☆46Updated 4 years ago
- Mumemto: multi-MUM and MEM finding across pangenomes☆79Updated 2 weeks ago
- VACmap: a long-read aligner specifically designed for complex structural variation discovery☆35Updated 5 months ago
- A reimplementation of the WaveFront Alignment algorithm at low memory☆49Updated 11 months ago
- Segmental Duplication Assembler (SDA).☆44Updated last year
- Tool for globally phasing diploid assembly graphs with orthogonal data☆39Updated 5 months ago
- TGS scaffolding☆46Updated 3 years ago
- ☆34Updated 5 years ago
- ☆34Updated 2 years ago
- Miscellaneous scripts for applications of PacBio systems☆27Updated 3 years ago
- MarginPolish: Graph based assembly polishing☆46Updated 4 years ago
- Compute N50/NG50 and auN/auNG☆31Updated last year
- Identification of transposable element families from pangenome polymorphisms☆45Updated last month
- Show pangenome graphs in an easy way☆55Updated 2 years ago
- ☆32Updated last week
- VarIant SimulatOR for short, long and linked reads☆48Updated 6 months ago
- GFAffix identifies walk-preserving shared affixes in variation graphs and collapses them into a non-redundant graph structure.☆36Updated last month
- SRF: Satellite Repeat Finder☆95Updated last year
- Evaluate variant calls and its combination with k-mer multiplicity☆66Updated 2 years ago
- Structural variant caller☆54Updated 3 years ago
- A C++ library and utilities for manipulating the Graphical Fragment Assembly format.☆54Updated 2 years ago
- MindTheGap is a SV caller for short read sequencing data dedicated to insertion variants (all sizes and types). It can also be used as a …☆37Updated 3 years ago
- base-accurate DNA sequence alignments using edlib and mashmap2☆33Updated 4 years ago
- SV genotyping with long reads☆40Updated last year
- A fast tool for detecting and decomposing segmental duplications in genome assemblies☆48Updated last year
- ☆48Updated 10 months ago
- A python script for finding telomeric repeats (TTAGGG/CCCTAA) in FASTA files☆33Updated 2 years ago
- ☆47Updated 4 years ago
- calling SVs from Blasr contig level alignments☆54Updated 7 years ago
- A tool for the recovery of unassembled telomeres from soft-clipped read alignments.☆36Updated 2 weeks ago