Fast and accurate de novo assembler for long reads
-
Updated
May 10, 2024 - C
Fast and accurate de novo assembler for long reads
Clair3 - Symphonizing pileup and full-alignment for deep learning-based long-read variant calling
PEPPER-Margin-DeepVariant
Reference-guided transcript discovery and quantification for long read RNA-Seq data
Highly parallelised multi-taxonomic profiling of shotgun short- and long-read metagenomic data
Long read production pipelines
Nanopore RNA-Seq data from the Singapore Nanopore-Expression Project
Tandem repeat expansion detection or genotyping from long-read alignments
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
ClairS - a deep-learning method for long-read somatic small variant calling
Graph-based assembly phasing
Yet Another Chimeric Read Detector
ClairS-TO - a deep-learning method for tumor-only somatic variant calling
Long-reads Gap-free Chromosome-scale Assembler
A fast tool for hybrid genome assembly of long and short reads
⛓ Long Interval Nucleotide K-mer Scaffolder
memory efficient, fast & precise taxnomomic classification system for metagenomic read mapping
SneakySnake:snake: is the first and the only pre-alignment filtering algorithm that works efficiently and fast on modern CPU, FPGA, and GPU architectures. It greatly (by more than two orders of magnitude) expedites sequence alignment calculation for both short and long reads. Described in the Bioinformatics (2020) by Alser et al. https://arxiv.o…
Add a description, image, and links to the long-reads topic page so that developers can more easily learn about it.
To associate your repository with the long-reads topic, visit your repo's landing page and select "manage topics."