Fast and accurate de novo assembler for long reads
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Updated
May 10, 2024 - C
Fast and accurate de novo assembler for long reads
Clair3 - Symphonizing pileup and full-alignment for high-performance long-read variant calling
PEPPER-Margin-DeepVariant
Reference-guided transcript discovery and quantification for long read RNA-Seq data
Long read production pipelines
Highly parallelised multi-taxonomic profiling of shotgun short- and long-read metagenomic data
abPOA: an SIMD-based C library for fast partial order alignment using adaptive band
Pipeline for calling structural variations in whole genomes sequencing Oxford Nanopore data
Nanopore RNA-Seq data from the Singapore Nanopore-Expression Project
A fast tool for hybrid genome assembly of long and short reads
ClairS - a deep-learning method for long-read somatic small variant calling
Tandem repeat expansion detection or genotyping from long-read alignments
Long-reads Gap-free Chromosome-scale Assembler
⛓ Long Interval Nucleotide K-mer Scaffolder
Yet Another Chimeric Read Detector
Graph-based assembly phasing
memory efficient, fast & precise taxnomomic classification system for metagenomic read mapping
Scalable long read self-correction and assembly polishing with multiple sequence alignment
ClairS-TO - a deep-learning method for tumor-only somatic variant calling
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