HiSeq 2500 System


9 Gb–1 Tb

output range

300 M–4 B

reads per run

2 × 250 bp

max read length
Progress in Rapid Identification of Variants Linked to Genetic Diseases
Progress in Rapid Identification of Variants Linked to Genetic Diseases

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.

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Precision Immunotherapies Using Tumor-Specific HLA Ligands

RNA-Seq and HLA typing are increasing the power and efficiency of a target discovery platform.

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Gleaning Genetic Insight about Neurodegenerative Disorders

TruSeq Neurodegeneration Panel enables researchers to investigate the complex genetic landscape of Alzheimer's, Parkinson's, and other neurodegenerative diseases.

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Decade of Sequencing Graphic

One Decade of Sequencing

Explore the breakthroughs, advancements, and progress

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HiSeq Rapid SBS Kit v2
HiSeq Rapid SBS Kit v2

HiSeq Rapid v2 SBS Kits enable the longest reads on HiSeq instruments, with reads up to 2x250 bp. The new kits generate up to 300 Gb of data per run. HiSeq Rapid SBS Kits v2 are the ideal choice for sequencing on HiSeq systems.

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TruSeq DNA Exome
TruSeq DNA Exome

This kit provides a low-cost exome sequencing solution that delivers exceptional target coverage over a broad range of read depths.

Nextera Flex for Enrichment
Nextera Flex for Enrichment

A fast, integrated workflow for a wide range of applications providing targeted resequencing for custom panels, fixed panels, and whole-exome enrichment.

HiSeq SBS Kit V4
HiSeq SBS Kit V4

Reagents for determining the DNA sequence of each cluster on a flow cell using sequencing by synthesis technology on enabled HiSeq systems.