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Nextera DNA kits provide a fast and easy library prep workflow, delivering whole-genome sequencing libraries in under 90 min.
This library preparation kit offers a gel-free method for preparing up to 12 kb mate pair libraries with the industry’s lowest DNA input requirement.
Custom target enrichment kit to rapidly interrogate those portions of the human genome most important to your specific research.
Identify coding variants up to 70% faster with this exome library prep and enrichment kit. Expanded kit sequences untranslated regions (UTRs) and miRNA.
A robust, scalable, and user-friendly workflow for transcriptome profiling of hundreds to tens of thousands of single cells in a given experiment.
Simple, cost-effective chromatin immunoprecipitation sequencing (ChIP-Seq) DNA library preparation, with master mixes and robust multiplex capabilities.
This library prep kit delivers sensitive and specific amplicon sequencing results from both low-input and FFPE DNA samples.
Focus on key genomic regions of interest with this targeted resequencing solution, useful for very high plexity pools or longer amplicons.
Converts bisulfite-treated, single-stranded DNA into an Illumina sequencing library. Enables comprehensive whole-genome DNA methylation analysis.
Simple, all-inclusive whole-genome sequencing (WGS) library preparation that provides accurate and comprehensive coverage of complex genomes.
This kit combines next-generation sequencing with epigenetic insights to accelerate biomarker discovery and understand methylation’s role in gene regulation.
Generate whole-genome sequencing libraries and efficiently interrogate samples with limited available DNA.
DNA library preparation for use with the NeoPrep System, providing comprehensive genomic coverage with low DNA input and minimal hands-on time.
Provides a reproducible, economical solution for sequencing RNA from FFPE tissues and other low-quality samples. Accuracy from as little as 10 ng total RNA.
The TruSeq RNA Library Preparation Kits provide a simple, cost-effective solution for analysis of the coding transcriptome.
The TruSeq Ribo Profile kit (formerly ARTseq) sequences ribosome-protected mRNA fragments to provide a snapshot of the active ribosomes in a cell.
A robust, highly scalable whole-transcriptome analysis (RNA-Seq) solution for a variety of species and sample types, including human, mouse, and FFPE.
Prepare whole-transcriptome sequencing libraries from blood-derived RNA with an efficient workflow that removes rRNA and globin mRNA in a single step.
Prepare sequencing libraries from mRNA to get a clear view of the coding transcriptome with strand-specific information.
Complete view of the transcriptome with walk-away workflow, lower input requirement, and excellent reproducibility.
Use this sequencing kit to prepare DNA libraries to generate synthetically long reads, with informatics options for genome assembly or genome phasing.
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.
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 enables cluster generation for subsequent paired-end sequencing on select HiSeq Systems as well as the HiScanSQ System.
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.
Designed for the rapid run mode of HiSeq 2500 and 1500 sequencers, these kits enable high data quality, fast turnaround time, and a walk-away workflow.
These kits contain ready-to-load reagents to determine the DNA sequence of each cluster on a HiSeq flow cell using sequencing by synthesis technology.
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.
BaseSpace Clarity LIMS is a laboratory information management system that helps laboratories track samples and optimize procedures and workflows.
BaseSpace Cohort Analyzer allows you to integrate and analyze subject and genomic data together using innovative visualization and analysis tools.
BaseSpace Correlation Engine mines over 20,000 genomic studies to get data-driven answers for genes, experiments, drugs and phenotypes for your research.
Simplify your bioinformatics with an economical and powerful computing environment to manage, analyze, and share data.
BaseSpace Variant Interpreter (Beta) enables genetic testing labs to rapidly annotate, filter, and interpret genomic data.
TruSight Inherited Disease is a targeted sequencing panel that focuses on 552 genes associated with severe, recessive pediatric onset diseases.
This panel focuses on exonic regions harboring disease-causing variants. Labs can perform commonly ordered molecular assays on-site with one assay.
TruSight Rapid Capture all-in-one kits enable targeted sequencing library preparation and enrichment for up to 96 samples in only 1.5 days.
Comprehensive next-generation sequencing (NGS) assay that targets DNA and RNA variants from the same FFPE sample.
This kit removes unwanted ribosomal RNA and globin mRNA from mammalian blood RNA samples before sequencing.
This kit removes cytoplasmic and mitochondrial rRNA from samples composed of human/mouse/rat, Gram-positive and Gram-negative bacterial RNA.
This kit removes both cytoplasmic and mitochondrial rRNA from human, mouse, and rat samples, including partially degraded samples.
This kit removes both cytoplasmic and mitochondrial ribosomal RNA from yeast samples.
This kit removes ribosomal RNA from Gram-positive and Gram-negative bacterial mixtures in a single pass.
This kit removes unwanted ribosomal RNA from Gram-negative bacterial samples.
This kit removes unwanted ribosomal RNA from Gram-positive bacterial samples.
This kit removes cytoplasmic ribosomal RNA from human, mouse, or rat samples, including partially degraded samples.
This kit removes cytoplasmic, mitochondrial, and chloroplast ribosomal RNA from plant seed, root, or leaf samples in a single pass.
These tubes enable sequencing sample tracking on the cBot 2 automated cluster generation system.
The cBot 2 System streamlines the sequencing workflow by automating cluster generation. It is a required accessory instrument for HiSeq sequencers.