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This kit enables cluster generation for subsequent sequencing on the HiSeq 3000 and HiSeq 4000 Systems.
Includes sequencing reagents specifically designed for the HiSeq 3000/HiSeq 4000 Systems. Enables production-scale sequencing for diverse applications.
Provides reagents for Single Read (SR) cluster generation on the cBot2 System. Cluster reagents are compatible with the HiSeq 3000 and HiSeq 4000 Systems.
This kit uses isothermal amplification to create clonal clusters of ~1000 copies each, ready for sequencing on enabled HiSeq systems.
HiSeq Rapid Cluster Kits v2 enable an on-board cluster generation process, designed to be used in HiSeq Rapid Run mode.
The HiSeq Rapid Duo cBot Sample Loading Kit doubles the indexing capability achieved with the on-board cluster generation process alone.
HiSeq Rapid SBS Kits v2 are designed for the rapid run mode of HiSeq 2500 and 1500 sequencers.
Reagents for determining the DNA sequence of each cluster on a flow cell using sequencing by synthesis technology on enabled HiSeq systems.
The HiSeq SR (Single Read) Cluster Kit v4 cBot uses isothermal amplification to create clonal clusters of ~1000 copies each, ready for sequencing on enabled HiSeq systems.
Kits include SBS reagents, clustering reagents, and patterned flow cells for increased cluster density and simplified image analysis, compared to non-patterned flow cells.
The MiSeq FGx Reagent Kit is specifically designed for use with the MiSeq FGx Forensic Genomics System.
Optimized chemistry to increase cluster density and read length, and improve sequencing quality scores, compared to earlier MiSeq reagent kit versions.
MiSeq sequencing reagents in pre-filled, ready-to-use cartridges. Micro and nano formats are available for low output applications.
MiniSeq Reagent Kits bring the power of Illumina NGS to labs of all sizes. Access cost-efficient sequencing, even for low numbers of samples.
These sequencing reagent kits offer a simplified workflow and improved data quality compared to the prior v1 kit version.
Reagent kits for the NovaSeq 5000 and NovaSeq 6000 Systems provide ready-to-use cartridge-based reagents for cluster generation and SBS.
PhiX Control v3 is a ready-to-use control library for Illumina sequencing runs.
These primers are required to sequence Nextera, TruSeq Synthetic Long-Read DNA, or TruSeq HT libraries in certain cases, as indicated.
This kit, when used with the cBot, enables cluster generation for subsequent paired-end sequencing on the Genome Analyzer IIx.
This kit enables cluster generation for subsequent paired-end sequencing on select HiSeq Systems as well as the HiScanSQ System.
This kit, when used with the Cluster Station, enables cluster generation for subsequent paired-end sequencing on the Genome Analyzer IIx.
TruSeq Rapid Cluster Kits - PE (paired-end) and SR (single-read) - are designed for use in the rapid run mode of HiSeq 2500 and 1500 sequencers.
This duo kit enables individually addressable lanes. It requires a cBot and is designed for the rapid run workflow of HiSeq 2500 and 1500 sequencers.
These SBS kits simplify batching and allow optimal indexing; enabling high data quality and fast turnaround high-throughput sequencing.
These kits contain ready-to-load reagents to determine the DNA sequence of each cluster on a flow cell using sequencing by synthesis (SBS) technology.
This sequencing kit for the Genome Analyzer IIx System permits users to extend read lengths to 2 x 150 and achieve up to 95 Gb of mappable data.
This kit provides reagents for cluster amplification on single-read flow cells. It is designed for use with the Genome Analyzer IIx with cBot.
Use this kit to cluster a flow cell on the cBot for subsequent single-read sequencing in the TruSeq v3 high output mode on enabled HiSeq systems.
This kit, when used with the Cluster Station, enables cluster generation for subsequent single-read sequencing on the Genome Analyzer IIx.
Use this interactive tool to explore cutting-edge experimental sequencing methods compiled from the scientific literature.
These short videos provide expert tips for common sequencing issues such as overclustering and inconsistent quantitation.
Our sequencing data analysis software helps you spend more time doing research, and less time configuring and running data analysis workflows.