Projects in Awesome Lists tagged with next-generation-sequencing
A curated list of projects in awesome lists tagged with next-generation-sequencing .
https://github.com/ablab/spades
SPAdes Genome Assembler
genome-assembly illumina metagenome-assembly next-generation-sequencing sequence-assembler sequencing transcriptome-assembly
Last synced: 21 Oct 2025
https://github.com/openbiox/awosome-bioinformatics
A curated list of resources for learning bioinformatics.
bioinformatics data-analysis next-generation-sequencing
Last synced: 08 Jan 2026
https://github.com/nf-core/sarek
Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
annotation bioinformatics cancer conda containers gatk4 genomics germline next-generation-sequencing nextflow nf-core pipeline pre-processing reproducible-research somatic target-panels variant-calling whole-exome-sequencing whole-genome-sequencing workflow
Last synced: 12 Feb 2026
https://github.com/sanger-pathogens/roary
Rapid large-scale prokaryote pan genome analysis
bioinformatics bioinformatics-pipeline genomics global-health infectious-diseases next-generation-sequencing pathogen research sequencing
Last synced: 21 Oct 2025
https://github.com/sanger-pathogens/Roary
Rapid large-scale prokaryote pan genome analysis
bioinformatics bioinformatics-pipeline genomics global-health infectious-diseases next-generation-sequencing pathogen research sequencing
Last synced: 02 Apr 2025
https://github.com/bioinformatics-centre/kaiju
Fast taxonomic classification of metagenomic sequencing reads using a protein reference database
bioinformatics metagenomics next-generation-sequencing taxonomic-classification taxonomy
Last synced: 21 Feb 2026
https://github.com/philres/ngmlr
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
alignment bioconda docker long-read mapper next-generation-sequencing oxford-nanopore pacbio structural-variations
Last synced: 14 Apr 2025
https://github.com/sanger-pathogens/snp-sites
Finds SNP sites from a multi-FASTA alignment file
bioinformatics bioinformatics-pipeline genomics global-health infectious-diseases next-generation-sequencing pathogen research sequencing
Last synced: 30 Dec 2025
https://github.com/nextstrain/nextclade
Viral genome alignment, mutation calling, clade assignment, quality checks and phylogenetic placement
clade clades coronavirus covid covid-19 covid19 dna influenza ncov neherlab next-generation-sequencing nextstrain research rna sars-cov-2 science sequences sequencing strain virus
Last synced: 15 Apr 2026
https://github.com/ngless-toolkit/ngless
NGLess: NGS with less work
bioinformatics bioinformatics-pipeline bwa fastq fastq-format genomics haskell haskell-language metagenomics next-generation-sequencing ngs samtools science
Last synced: 16 May 2025
https://github.com/xjtu-omics/msisensor-pro
Microsatellite Instability (MSI) detection using high-throughput sequencing data.
dna-missmatch-repair-system hypermutation microsatellite-instability next-generation-sequencing tumor-only-support
Last synced: 01 Apr 2026
https://github.com/chasewnelson/snpgenie
Program for estimating πN/πS, dN/dS, and other diversity measures from next-generation sequencing data
diversity-measurement dnds dnds-estimation evolution evolutionary-parameters fasta-sequences molecular-evolution natural-selection nei-gojobori next-generation-sequencing nucleotide nucleotide-diversity perl population-genetics sequence-analysis snp-report substitution-rate vcf vcf-files
Last synced: 23 Mar 2025
https://github.com/stjude-rust-labs/fq
Command line utility for manipulating Illumina-generated FASTQ files.
bioinformatics fastq fastq-files genomics illumina next-generation-sequencing rust
Last synced: 21 Oct 2025
https://github.com/Cibiv/NextGenMap
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.
c-plus-plus-11 next-generation-sequencing opencl short-read-mapper
Last synced: 19 Apr 2025
https://github.com/chanzuckerberg/czid-web
Infectious Disease Sequencing Platform
bioinformatics bioinformatics-pipeline biology chan-zuckerberg-id computational-biology czid genomics global-health infectious-diseases metagenomic next-generation-sequencing research science sequencing virology
Last synced: 10 Apr 2025
https://github.com/tobiasrausch/atacseq
Analysis Workflow for Assay for Transposase-Accessible Chromatin using sequencing (ATAC-Seq)
atac-seq atac-seq-pipeline chromatin next-generation-sequencing nucleosome-positioning peak-detection sequencing
Last synced: 18 Mar 2026
https://github.com/epigen/mrbiomics
MrBiomics: Modules & Recipes augment Bioinformatics for Multi-Omics Analyses
automation bioinformatics biomedical data-science epigenetics framework genetics genomics modules next-generation-sequencing python r recipes research science snakemake workflows
Last synced: 23 Jun 2025
https://github.com/stjudecloud/workflows
Bioinformatics workflows developed for and used on the St. Jude Cloud project.
bioinformatics bioinformatics-workflows computational-biology cromwell cwl cwl-workflow genomics next-generation-sequencing stjudecloud wdl wdl-workflow workflow workflow-engine workflows
Last synced: 19 Feb 2026
https://github.com/zhanxw/seqminer
Query sequence data (VCF/BCF1/BCF2, Tabix, BGEN, PLINK) in R
annotation bcf bgen meta-analysis next-generation-sequencing plink sequencing tabix vcf workflow
Last synced: 18 Feb 2026
https://github.com/ncbi/pm4ngs
Project Manager for NGS data analysis
bioinformatics chipexo chipseq cwl-workflow next-generation-sequencing ngs-analysis ngs-pipeline rnaseq
Last synced: 04 Jul 2025
https://github.com/sanger-pathogens/mlst_check
Multilocus sequence typing by blast using the schemes from PubMLST
bioinformatics bioinformatics-pipeline genomics global-health infectious-diseases next-generation-sequencing pathogen research sequencing
Last synced: 21 Feb 2026
https://github.com/stjudecloud/wdldoc
Create WDL documentation using Markdown.
bioinformatics computational-biology cromwell genomics next-generation-sequencing stjudecloud wdl wdl-workflow workflow
Last synced: 13 Apr 2025
https://github.com/TimoLassmann/samstat
SAMStat displays various properties of next-generation sequencing reads stored in SAM/BAM format.
bioinformatics next-generation-sequencing quality-control
Last synced: 05 May 2025
https://github.com/genometric/mspc
Using combined evidence from replicates to evaluate ChIP-seq peaks
analysis chip-seq enriched-regions genome-analysis mspc next-generation-sequencing ngs-analysis overlapping-peaks peak peaks
Last synced: 12 Apr 2025
https://github.com/futianfan/genocraft
GenoCraft: A Comprehensive, User-Friendly Web Platform for High-Throughput Omics Data Analysis and Visualization (https://arxiv.org/pdf/2312.14249)
bulk-rna-seq flask genomics multiomics next-generation-sequencing ngs omics omics-data-integration pathway-analysis protein rna-seq single-cell visualization
Last synced: 12 Oct 2025
https://github.com/chgibb/PHAT
Pathogen-Host Analysis Tool - A modern Next-Generation Sequencing (NGS) analysis platform
alignment analysis bam bam-files bioinformatics bioinformatics-analysis bioinformatics-tool circos circos-graphs circos-plot dna electron host next-generation-sequencing ngs pathogen phat quality-control snps visualization
Last synced: 05 May 2025
https://github.com/epigen/fetch_ngs
Workflow to Fetch Public Sequencing Data and Metadata Using iSeq and MrBiomics Module.
bam database fastq genomics next-generation-sequencing ngs repository
Last synced: 14 Sep 2025
https://github.com/stjudecloud/ngsderive
Forensic analysis tool useful in backwards computing information from next-generation sequencing data.
bioinformatics computational-biology gene-model genomics next-generation-sequencing ngs strandedness strandedness-inference workflow workflow-engine
Last synced: 11 Jul 2025
https://github.com/fls-bioinformatics-core/auto_process_ngs
Scripts and utilities for automatic processing & management of Illumina NGS sequencing data within the Bioinformatics Core Facility at the University of Manchester
10xgenomics automation bioinformatics fastq-files illumina next-generation-sequencing pipeline qc sequencing
Last synced: 23 Jan 2026
https://github.com/multiqc/example-plugin
A miniature example of a MultiQC plugin.
example-project multiqc multiqc-plugin next-generation-sequencing ngs plugin python quality-control
Last synced: 05 May 2025
https://github.com/bihealth/cnvetti
:tada: CNVetti – robust, efficient, and versatile clinical CNV calling from HTS data
bioinformatics copy-number-variation next-generation-sequencing
Last synced: 12 Feb 2026
https://github.com/kohyamat/massgenotyping
Python package for microsatellite genotyping from highly multiplexed amplicon sequencing data
amplicon-sequencing genotyping microsatellite next-generation-sequencing
Last synced: 14 Jan 2026
https://github.com/wpwupingwp/divide
Divide NGS data by barcode and primer
dna-barcode-extraction next-generation-sequencing
Last synced: 17 Jan 2026
https://github.com/dfornika/miseq-samplesheet-parser
Parse illumina MiSeq SampleSheet.csv files and convert to JSON
bioinformatics illumina miseq next-generation-sequencing
Last synced: 20 May 2026
https://github.com/ngless-toolkit/nglesspy
NGLess as a Python embedded language (experimental)
domain-specific-language embedded-language experimental genomics metagenomics next-generation-sequencing ngless python python-embedded-language
Last synced: 06 Apr 2025
https://github.com/sivkri/small-rna-seq-analysis
scripts and resources for performing miRNA sequencing analysis using tools like mirPRo and miRDeep2. Explore the code to process reads, map them to the genome, quantify known miRNAs, identify novel miRNAs, and browse the results
bioinformatics gene-expression-analysis mirna mirna-seq mirna-sequencing next-generation-sequencing rna-seq-analysis small-rna-analysis
Last synced: 19 May 2026
https://github.com/carpentries-incubator/scrna-seq-analysis
Single-cell RNA Sequencing Data Analysis
bioinformatics lesson next-generation-sequencing pre-alpha scrna-seq single-cell single-cell-rna-seq
Last synced: 02 Sep 2025
https://github.com/m-jahn/crispri-lib-pipe
Pipeline to process CRISPRi library sequencing data
bioinformatics-pipeline functional-genomics next-generation-sequencing pipeline python
Last synced: 25 Apr 2026
https://github.com/phac-nml/submitdatairidanext
Pipeline for submitting data to INSDC databases for IRIDA Next
data-sharing data-submission file-transfer microbial-genomics next-generation-sequencing
Last synced: 16 Jan 2026
https://github.com/fullscreen-triangle/gospel
Framework for comprehensive variant detection in whole genome sequences using advanced machine learning models for cross domain pattern recognition in fitness, pharmacogenetics and nutritional aspects of sprint running
exome-sequencing next-generation-sequencing pharmacogenetics variant-analysis variant-calling whole-genome-sequencing
Last synced: 16 Aug 2026
https://github.com/neurogenomics/epiprepare
Preprocessing of epigenomic data from fastq files.
epigenomics next-generation-sequencing preprocessing r r-package
Last synced: 27 Jul 2025
https://github.com/astrabert/rrequested
RREQUESTED: A versatile shellscript tool based on Python scripts to preprocess raw basecalled reads with quality and size filtering and ex-novo demultiplexing
beginner-friendly bioinformatics conda demultiplexing easy-to-use genomics next-generation-sequencing oxford-nanopore
Last synced: 05 Mar 2025
https://github.com/mpusp/snakemake-simple-mapping
A Snakemake workflow for the mapping of reads to reference genomes, minimalistic and simple.
bowtie2 bwa-mem2 genomics mapping next-generation-sequencing snakemake snakemake-workflow star-alignment variant-calling
Last synced: 11 Mar 2026
https://github.com/ngless-toolkit/ngless2018benchmark
Benchmarking ngless
benchmark benchmarking benchmarking-ngless bioinformatics next-generation-sequencing ngless
Last synced: 12 Aug 2025
https://github.com/jcaperella29/bwa_samtools_cwl_flow
a common language workflow , workflow to process Fastq files
bioinformatics cwl-workflow next-generation-sequencing
Last synced: 07 Mar 2026
https://github.com/starsareintherose/rgbepp
Reference Genome based Exon Phylogeny Pipeline
exome exome-sequencing exome-sequencing-analysis next-generation-sequencing phylogeny
Last synced: 18 Jan 2026
https://github.com/gmauro/presta
Presta handles sequencing data produced from a large scale NGS Core facility. It leverages a reliable distributed task queue to create a messages-driven automation system. Presta is focused on real-time operations, but supports scheduling as well.
message-queue next-generation-sequencing python python-library
Last synced: 29 Mar 2025
https://github.com/tus-kondolab/iso2gene
Cross-platform C/C++ implementation of the tximport algorithm for gene-level quantification
next-generation-sequencing ngs rna-seq rnaseq tximport windows
Last synced: 08 Jun 2026
https://github.com/scholl-lab/plasmicheck
Detect and quantify plasmid DNA contamination in sequencing data
bioinformatics contamination-detection genomics minimap2 next-generation-sequencing plasmid splicing
Last synced: 18 Feb 2026
https://github.com/player-alex/fastx-toolkit
High-performance FASTQ/FASTA processing toolkit with optimized block-based I/O and OpenMP parallelization.
bioinformatics bioinformatics-tool cmake cpp cpp17 cross-platform fasta fastq fastq-parser format-conversion genomics high-performance next-generation-sequencing ngs openmp parallel-processing performance-optimization quality-control sequence-analysis sequencing
Last synced: 03 May 2026
https://github.com/bccdc-phl/routine-sequence-qc-collector
Collect outputs from BCCDC-PHL/routine-sequence-qc pipeline for usage by BCCDC-PHL/routine-sequence-qc-site
data-management microbial-genomics next-generation-sequencing quality-control
Last synced: 29 Jan 2026