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iRNA-seq: computational method for genome-wide assessment of acute transcriptional regulation from total RNA-seq data.
Nucleic Acids Res 43 e40 2015
Targeted Next-Generation Sequencing Identifies a Recurrent Mutation in MCPH1 Associating with Hereditary Breast Cancer Susceptibility.
PLoS Genet 12 e1005816 2016
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.
Explore Tools
Provides an overview of instrument components and instructions for operating and maintaining the HiSeq 2500.
Lab specifications and requirements for preparing the lab for sequencing on the HiSeq 2500 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.
Support resources including guides, upgrade resources, and the latest support updates for the HiSeq 2500.
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.
Learn how DNA sequencing is leading to progress in the rapid identification of variants that might be involved in genetic diseases. Thanks to this work, Dr. Kingsmore and his team now hold a Guinness World Records title.
View VideoResearchers rely on transcriptomics to uncover multiple drug-susceptible tumorigenic pathways.
Read ArticleNew Zealand–based research group uses GBS to overcome cost and resource hurdles associated with genomic selection for orphan crops and minor livestock species.
Read Article
David Goldstein at the Center for Human Genome Variation shares how sequencing with the HiSeq 2500 helps advance neuropsychiatry.
Learn how tomato circadian clocks and genes evolved as tomatoes were transferred from their equatorial birthplace and planted across North America.
Learn how transplanting gut microbes from patients diagnosed with depression affects the mental state of germ-free mice.