lh3 / kmer-cntLinks
Code examples of fast and simple k-mer counters for tutorial purposes
☆170Updated 5 years ago
Alternatives and similar repositories for kmer-cnt
Users that are interested in kmer-cnt are comparing it to the libraries listed below
Sorting:
- SIMD partial order alignment tool/library☆170Updated last month
- A fast K-mer counter for high-fidelity shotgun datasets☆131Updated last month
- A fast approximate aligner for long DNA sequences☆284Updated last year
- Aligns short reads using dynamic seed size with strobemers☆181Updated this week
- Pairwise whole genome aligner☆198Updated 3 weeks ago
- Wavefront alignment algorithm (WFA): Fast and exact gap-affine pairwise alignment☆200Updated 3 years ago
- abPOA: an SIMD-based C library for fast partial order alignment using adaptive band☆130Updated last week
- Graphical Fragment Assembly (GFA) Format Specification☆215Updated last year
- Tools for manipulating sequence graphs in the GFA and rGFA formats☆238Updated last year
- Assembled Genomes Compressor☆169Updated 11 months ago
- Long read / genome alignment software☆303Updated 11 months ago
- Global alignment and alignment extension☆138Updated 2 years ago
- CCS: Generate Highly Accurate Single-Molecule Consensus Reads (HiFi Reads)☆124Updated last year
- A complete diploid human genome☆136Updated last month
- Read Until client library for Nanopore Sequencing☆106Updated last year
- a signal-level demultiplexer for Oxford Nanopore reads☆126Updated 4 years ago
- Hierarchical Alignment Format☆172Updated last month
- Bifrost: Highly parallel construction and indexing of colored and compacted de Bruijn graphs☆219Updated last week
- base-accurate DNA sequence alignments using WFA and mashmap3☆206Updated last month
- Yet another k-mer analyzer☆149Updated 3 weeks ago
- Program for aligning DNA sequences, a pairwise aligner.☆230Updated 4 months ago
- A tool to identify, orient, trim and rescue full length cDNA reads☆83Updated 3 years ago
- Fast multi-line FASTA/Q reader in several programming languages☆176Updated 4 years ago
- Find all significant local alignments between reads☆141Updated last year
- a Bioinformatics Application for Navigating De novo Assembly Graphs Easily☆150Updated last month
- pbsv - PacBio structural variant (SV) calling and analysis tools☆160Updated 8 months ago
- De novo genome assembler for long uncorrected reads☆226Updated last year
- Oxford Nanopore Technologies fast5 API software☆154Updated last year
- Training models for basecalling Oxford Nanopore reads☆115Updated 3 years ago
- Research release basecalling models and configurations☆115Updated 5 months ago