Describes instrument components, on-instrument software, the sequencing workflow, and maintenance procedures for the HiSeq 4000.
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.
Describes instrument components, on-instrument software, the sequencing workflow, and maintenance procedures for the HiSeq 4000.
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.
The site prep guide contains lab specifications and requirements for preparing the lab for sequencing on the HiSeq 3000 or HiSeq 4000 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.
Access guides, literature, and technical notes for the HiSeq 3000 System.
Access guides, literature, and technical notes for the HiSeq 4000 System.
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.
Watch VideoResearchers in India study a deadly oral cancer that is strongly associated with chewing tobacco together with slaked lime.
Read articleIntegrating imaging, multiomic technologies, and big data uncovers novel diagnostic and therapeutic targets for common chronic diseases.
Read articleIncrease your throughput and coverage depth with the increased capacity of the HiSeq 3000 and HiSeq 4000 Systems.
Learn how to harness the power of the HiSeq 3000 and HiSeq 4000 Systems for your diverse high-throughput sequencing applications.
Discover how linked-reads and phased genome analysis provide insights in human genetics and oncology.
Demonstration of high-throughput NGS methods on the HiSeq 4000 instrument, focusing on the exome sequencing workflow.
Learn how the UCSF Center for Advanced Technology transitioned from the HiSeq 2500 System to the HiSeq 4000 System.