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Assay targeting multiple variant types, including tumor mutational
burden (TMB) and microsatellite instability (MSI), even from
Perform transcriptome profiling for hundreds to tens of thousands
of single cells in one experiment.
Scalable throughput and flexibility for virtually any genome,
sequencing method, and scale of project.
A fast, integrated workflow for a wide range of applications, from
human whole-genome sequencing to amplicons, plasmids, and
Somatic mutations in cerebral cortical malformations.
N Engl J Med 371 733-43 2014
The Gut Microbiota of Rural Papua New Guineans: Composition, Diversity Patterns, and Ecological Processes.
Cell Rep 2015
Development of a Comprehensive Sequencing Assay for Inherited Cardiac Condition Genes.
J Cardiovasc Transl Res 9 3-11 2016
Find the right library prep kit or microarray, calculate sequencing coverage, explore methods, design custom assays, and more.
Information about instrument components, software, required products, performing a sequencing run, and instrument maintenance.
Find lab specifications and requirements for preparing your lab for a MiSeq System.
Online Illumina sequencing courses are free, interactive, and available any time.
This tool will help you determine the best hands-on sequencing training for your needs based on your area of interest, application, library preparation kit, and platform.
Sequencing coverage describes the average number of NGS reads that align to known reference bases. Coverage requirements vary by application.
Additional information about sequencing quality scores, how they are calculated, and the relationship between quality score and base call accuracy.
Find system guides, related application and technical notes, and other supporting documentation for the MiSeq System.
These short videos provide expert tips for common sequencing issues such as overclustering and inconsistent quantitation.
The Custom Protocol Selector enables you to generate your own customized documentation, specifically tailored to your experiment.
The DRAGEN platform enables GeneDx to scale to whole-genome analysis and identify variants with precision.
NGS expands genomic projects for species ancient and new, large and small.
Practical information for new MiSeq users with many tips, tricks, and microbial examples gleaned from long instrument experience.
Researchers used paired-end 16S amplicon sequencing on the MiSeq System to explore their microbe-cycling hypothesis.
Researchers compared viral RNA sequences from samples, and found substitutions absent from other Western African Ebola genomes.
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