ClairS - a deep-learning method for long-read somatic small variant calling
-
Updated
Aug 16, 2024 - Python
ClairS - a deep-learning method for long-read somatic small variant calling
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…
🍶 Genome assembly with short sequence reads
Better and faster Rust implementation of the FragGeneScan gene prediction model for short and error-prone reads.
Genotyping of segregating mobile elements insertions
VStrains is a de novo approach for reconstructing strains from viral quasispecies.
FQSqueezer - FASTQ compressor based on k-mer statistics
A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region expansions (RREs) from short DNA reads
A scalable variant calling and benchmarking framework supporting both short and long reads.
A pipeline to identify (and remove) certain sequences from raw genomic data. Default taxa to identify (and remove) are Homo and Homo sapiens. Removal is optional.
GateSeeder is the first near-memory CPU-FPGA co-design for alleviating both the compute-bound and memory-bound bottlenecks in short and long-read mapping. GateSeeder outperforms Minimap2 by up to 40.3×, 4.8×, and 2.3× when mapping real ONT, HiFi, and Illumina reads, respectively.
A nextflow pipeline for calling and annotating small germline variants from short DNA reads for WES and WGS data
TAIFA is a workflow for conducting Whole-Genome Sequencing (WGS) of bacteria
Evolutionary genomics of chromosomal inversions in Atlantic herring
Short read mapping and variant calling
A flexible complex genome rearrangement simulator for short and long reads
Nextflow pipeline for short-read alignment
Synthetically Engineered Wastewater sequence data for Assessing Genomic Entities
A nextflow pipeline to calculate depth of coverage from a metagenomic set of bins
Add a description, image, and links to the short-reads topic page so that developers can more easily learn about it.
To associate your repository with the short-reads topic, visit your repo's landing page and select "manage topics."