Olivar: towards automated variant aware primer design for multiplex tiled amplicon sequencing of pathogens
-
Updated
May 12, 2025 - Python
Olivar: towards automated variant aware primer design for multiplex tiled amplicon sequencing of pathogens
A tool in order to accurately remove primer sequences from NGS reads in an amplicon experiment
gNOMO2 allows integrated multi-omics analyses of microbiomes
Python package for microsatellite genotyping from highly multiplexed amplicon sequencing data
A pipeline for variant calling from P. falciparum short reads generated from Illumina and ONT libraries
CRISPRSeqSim is a tool that simulates results of CRISPR/cas editing fragments target sequencing.
A snakemake pipeline for amplicon (16S, 18S, ITS) sequence analysis using Usearch.
Pipeline for amplicon sequencing projects. OTUs can be build with various methods (usearch,vsearch,uparse,swarm) and classified using the RDP Classifier and SINA. Final output is a BIOM file for downstream processing (Phyloseq/R)
Bioinformatics pipeline for processing Hantavirus NGS data with a two-pass approach. Implements quality control, reference-based mapping, metaconsensus refinement, variant calling, and automatic negative sample detection. Features include primer evaluation, coverage visualization, and comparison between consensus sequences.
Add a description, image, and links to the amplicon-sequencing topic page so that developers can more easily learn about it.
To associate your repository with the amplicon-sequencing topic, visit your repo's landing page and select "manage topics."