bluenote-1577 / deviderLinks
Dividing heterogeneous long-read sequencing into groups with de Bruijn graphs
☆40Updated 4 months ago
Alternatives and similar repositories for devider
Users that are interested in devider are comparing it to the libraries listed below
Sorting:
- Software that separates very close sequences that have been collapsed during assembly. Uses only long reads.☆35Updated 9 months ago
- Correcting errors in noisy long reads using variation graphs☆50Updated 3 years ago
- ☆46Updated 2 months ago
- Strain-level haplotyping for metagenomes with short or long-reads.☆63Updated 9 months ago
- Fast long-read mapper and whole-genome aligner (accelerated version of minimap2)☆36Updated last month
- Genome size estimation from long read overlaps☆80Updated 2 months ago
- GFAffix identifies walk-preserving shared affixes in variation graphs and collapses them into a non-redundant graph structure.☆37Updated 8 months ago
- Wavefront alignment algorithm (WFA) in Golang☆32Updated 6 months ago
- Long read aligner for cyclic and acyclic pangenome graphs☆40Updated 2 years ago
- Extracting paths from assembly graphs☆24Updated last year
- Differential k-mer analysis☆39Updated 2 years ago
- Pangenome Sequence Naming: a backwards-compatible hack to simplify the identification of samples and haplotypes in pangenomes☆44Updated last year
- Kmer Analysis of Pileups for Genotyping☆35Updated last week
- Remove human reads from a sequencing run☆47Updated last month
- A novel method for sequence similarity estimation☆28Updated last year
- Python wrapper for wavefront alignment using WFA2-lib☆38Updated last year
- Statistics and analysis for variation graphs☆48Updated last year
- Improved Phased Assembler☆28Updated 3 years ago
- General purpose utility related to GAF files☆29Updated 2 weeks ago
- PG-SCUnK mesure quality of Pan-Genome Graphs using Single Copy and Universal k-mers☆23Updated last week
- Improved long-read assembly by preserving contained reads☆30Updated last year
- fast, multithreaded sourmash operations: search, compare, and gather.☆25Updated last week
- somatic SV calling on matched tumor-normal co-assembly graphs☆22Updated last year
- R package and wrapper functions for identifying serial structural variations from genome assemblies☆29Updated last year
- Better Alignments with Translated HMMER☆24Updated this week
- Panache is a web-based interface designed for the visualization of linearized pangenomes. It can be used to show presence/absence informa…☆47Updated 2 years ago
- Code to create a PRG from a Multiple Sequence Alignment file☆25Updated 4 months ago
- Linear-time de novo Long Read Assembler☆41Updated 3 months ago
- convert variation graph alignments to coverage maps over nodes☆27Updated 2 weeks ago
- A bioinformatics tool written in Rust to find palindromic sequences in DNA☆38Updated 5 months ago