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Comprehensive panel detects single-nucleotide variants (SNVs), amplifications, and fusions that contribute to solid tumor progression.
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 microbial species.
Use this guide to help you evaluate important factors and choose the right next-generation sequencing instrument for your lab.
This interactive tool will help you compare sequencers and find the one that’s right for your lab or application.
Compare the iSeq 100 System with other Illumina benchtop sequencers.
This infographic describes how NGS can help you overcome the limitations of qPCR and Sanger sequencing.
Learn how targeted NGS can help you gain greater insight in your studies and save time compared to traditional methods.
See Illumina sequencing by synthesis (SBS) technology in action and learn how it works.
Find kits, methods, and automation solutions to help you prepare DNA or RNA libraries before sequencing.
Our software simplifies sequencing data analysis, so you can focus on your research instead of setting up analysis workflows.
This detailed overview describes the basics of Illumina sequencing technology, key methods, and more.
Learn the key differences between NGS and Sanger sequencing and determine when NGS can be a more effective option.
Compare the benefits of NGS technology to qPCR and learn which one to choose.
Explore different buying options—including leasing, bundles, trade-in offers, and more—to find one that fits your needs.
This document offers specification information and other resources to help you justify funding for the iSeq 100 System.
Acquire the advanced technology you need now through fast, easy, and affordable financing and leasing programs.
Find supporting documentation for the iSeq 100 System.
Online Illumina sequencing courses are free, interactive, and available any time.
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.
These short videos provide expert tips for common sequencing issues such as overclustering and inconsistent quantification.
New to Illumina technology? See step-by-step guidance to help you transition your studies.
Find workflow guidance from Illumina experts, including considerations for hotspot resequencing with AmpliSeq for Illumina Cancer Hotspot Panels.
View tips on transitioning to the Nextera DNA Flex Library Prep Kit, including considerations for viral and bacterial whole-genome sequencing.
See our detailed guides designed to help you transfer projects from TruSeq Custom Amplicon to AmpliSeq for Illumina panels.
Determine the best sequencing library preparation kit for your needs based on your project type, starting material, and method of interest.
Identify sequencing panels that target your genes of interest.
Find interactive tools designed to help you choose the right products for your needs and plan your experiments.
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