There are 20 repositories under next-generation-sequencing topic.
A curated list of resources for learning bioinformatics.
Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
Rapid large-scale prokaryote pan genome analysis
NGMLR is a long-read mapper designed to align PacBio or Oxford Nanopore (standard and ultra-long) to a reference genome with a focus on reads that span structural variations
Fast taxonomic classification of metagenomic sequencing reads using a protein reference database
Artemis is a free genome viewer and annotation tool that allows visualization of sequence features and the results of analyses within the context of the sequence, and its six-frame translation
Finds SNP sites from a multi-FASTA alignment file
A tool to circularize genome assemblies
Viral genome alignment, mutation calling, clade assignment, quality checks and phylogenetic placement
Antimicrobial Resistance Identification By Assembly
Rapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins
NGLess: NGS with less work
An efficient FASTQ manipulation suite
Detect germline or somatic variants from normal or tumour/normal whole-genome or targeted sequencing
Get assembly statistics from FASTA and FASTQ files
Program for estimating πN/πS, dN/dS, and other diversity measures from next-generation sequencing data
Microsatellite Instability (MSI) detection using high-throughput sequencing data.
Dockerised Next Generation Sequencing Pipeline (QC, Align, Calling, Annotation)
NextGenMap is a flexible highly sensitive short read mapping tool that handles much higher mismatch rates than comparable algorithms while still outperforming them in terms of runtime. This allows analysing large scale datasets even with increased SNP rates or higher error rates (e.g. caused by specialized experimental protocols) and avoids biases caused by highly variable regions in the genome.
DeepMicrobes: taxonomic classification for metagenomics with deep learning
Infectious Disease Sequencing Platform
Analysis Workflow for Assay for Transposase-Accessible Chromatin using sequencing (ATAC-Seq)
Python3 scripts to manipulate FASTA and FASTQ files
Command line utility for manipulating Illumina-generated FASTQ files.
Improve the quality of a denovo assembly by scaffolding and gap filling
de novo virus assembler of Illumina paired reads
A high throughput sequence read toolset using a streaming approach facilitated by Linux pipes
DNAscan is a fast and efficient bioinformatics pipeline that allows for the analysis of DNA Next Generation sequencing data, requiring very little computational effort and memory usage.
An opinionated Cromwell orchestration manager.
Enhanced and elegant flexible peak/loop/domain -calling and analysis tool for 1D/3D genomic data.
A tool for genotyping Variable Number Tandem Repeats (VNTR) from sequence data
AMPtk: Amplicon ToolKit for NGS data (formally UFITS)