SPAdes Genome Assembler
-
Updated
Dec 25, 2024 - C++
SPAdes Genome Assembler
Java utilities for Bioinformatics
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
Finds SNP sites from a multi-FASTA alignment file
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
A tool to circularize genome assemblies
Viral genome alignment, mutation calling, clade assignment, quality checks and phylogenetic placement
Rapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins
Antimicrobial Resistance Identification By Assembly
NGLess: NGS with less work
An efficient FASTQ manipulation suite
Rare variant test software for next generation sequencing data
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.
Add a description, image, and links to the next-generation-sequencing topic page so that developers can more easily learn about it.
To associate your repository with the next-generation-sequencing topic, visit your repo's landing page and select "manage topics."