研究を推進するためのHiSeq 3000/HiSeq 4000 製品資料

生産規模のゲノミクスをサポートする製品資料、お客様事例、およびウェビナー

HiSeq 3000/HiSeq 4000 製品資料

お客様のニーズに最適な製品を選択し、実験を計画するのに役立つインタラクティブなツールをご紹介します。

ツールを利用する
製品選択ツールおよび実験計画ツール
HiSeq 3000 User Guide

Describes instrument components, on-instrument software, the sequencing workflow, and maintenance procedures for the HiSeq 4000.

Access PDF
Sequencing Online Training

Online Illumina sequencing courses are free, interactive, and available any time.

Find Training
Personalized Training Workflow Selection Tool

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.

Learn More
HiSeq 4000 User Guide

Describes instrument components, on-instrument software, the sequencing workflow, and maintenance procedures for the HiSeq 4000.

Access PDF
Sequencing Coverage

Sequencing coverage describes the average number of NGS reads that align to known reference bases. Coverage requirements vary by application.

Learn More
Quality Scores

Additional information about sequencing quality scores, how they are calculated, and the relationship between quality score and base call accuracy.

Learn More
HiSeq 3000/HiSeq 4000 Site Prep Guide

The site prep guide contains lab specifications and requirements for preparing the lab for sequencing on the HiSeq 3000 or HiSeq 4000 System.

Access PDF
Sequencing Troubleshooting Tips

These short videos provide expert tips for common sequencing issues such as overclustering and inconsistent quantitation.

Learn More
Custom Protocol Selector

The Custom Protocol Selector enables you to generate your own customized documentation, specifically tailored to your experiment.

Create Protocols
HiSeq 3000 Support Documentation

Access guides, literature, and technical notes for the HiSeq 3000 System.

View Documentation
HiSeq 4000 Support Documentation

Access guides, literature, and technical notes for the HiSeq 4000 System.

View Documentation
Progress in Rapid Identification of Variants Linked to Genetic Disease
Progress in Rapid Identification of Variants Linked to Genetic Disease

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 Video

Large-Scale Bull Genome Sequencing Enables Rapid Livestock Improvement

WGS data from the 1000 Bull Genomes Project is aiding discoveries of positive and negative traits, benefiting herds globally.

記事を読む
NGS Identifies Rare Disease Variants in Infants with Undiagnosed Disease

Landmark NGS study leads to a national clinical diagnostic exome sequencing platform in Singapore.

記事を読む

Illumina High Throughput Sequencing Portfolio Video
Illumina High Throughput Sequencing Portfolio Video

Increase your throughput and coverage depth with the increased capacity of the HiSeq 3000 and HiSeq 4000 Systems.

Watch Video