ncbi / ncbi-cxx-toolkit-publicLinks
NCBI C++ Toolkit package sources
☆86Updated this week
Alternatives and similar repositories for ncbi-cxx-toolkit-public
Users that are interested in ncbi-cxx-toolkit-public are comparing it to the libraries listed below
Sorting:
- GCLib - Genomic C++ library of reusable code for bioinformatics projects☆38Updated 6 months ago
- Bio++ Program Suite☆18Updated 2 weeks ago
- Viral Annotation DefineR: classification and annotation of viral sequences based on RefSeq annotation☆114Updated 3 weeks ago
- MIRROR OF: The European Molecular Biology Open Software Suite (from git://anonscm.debian.org/debian-med/emboss.git)☆29Updated 3 years ago
- Scalable annotated de Bruijn graphs for DNA indexing, alignment, and assembly☆215Updated last week
- A genomic k-mer counter (and sequence utility) with nice features.☆158Updated 6 months ago
- memory efficient, fast & precise taxnomomic classification system for metagenomic read mapping☆63Updated last week
- Fast hash function for DNA/RNA sequences☆106Updated last year
- ☆36Updated 9 months ago
- Codon's bioinformatics module☆57Updated 5 months ago
- Align multiple amino acid or nucleotide sequences.☆70Updated 5 years ago
- Slow5tools is a toolkit for converting (FAST5 <-> SLOW5), compressing, viewing, indexing and manipulating data in SLOW5 format.☆103Updated this week
- ClairS - a deep-learning method for long-read somatic small variant calling☆102Updated last week
- BioC++ core library (alphabet, meta, ranges)☆22Updated 2 years ago
- Building the compacted de Bruijn graph efficiently from references or reads.☆92Updated this week
- A versatile compressor of third generation sequencing reads.☆52Updated last year
- ☆108Updated last month
- Quality control tools for nanopore sequencing data☆111Updated last year
- HIVDB Genotypic Resistance Interpretation Program☆21Updated last week
- A fast multiple sequence alignment program.☆151Updated 6 months ago
- User-friendly software for viewing and processing Sanger DNA sequencing trace files.☆32Updated 7 years ago
- De novo clustering of long transcript reads into genes☆70Updated 9 months ago
- ☆53Updated last week
- cDNA read preprocessing☆83Updated last year
- Incremental building of phylogenetic distance trees☆27Updated this week
- ganon2 classifies genomic sequences against large sets of references efficiently, with integrated download and update of databases (refse…☆103Updated 3 weeks ago
- A easy-to-use Python API for Primer3 primer design.☆16Updated 3 years ago
- Portable WDL workflows for CZ ID production pipelines☆51Updated 7 months ago
- Variant calling tool for long-read sequencing data☆117Updated 10 months ago
- ☆16Updated 10 months ago