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Nextera DNA kits provide a fast and easy library prep workflow, delivering whole-genome sequencing libraries in under 90 min.
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 provides a low-cost exome sequencing solution that delivers exceptional target coverage over a broad range of read depths.
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.
This exome sequencing library prep kit uses a simple, one-day workflow to provide a fast path to greater understanding of the human exome.
The TruSeq Ribo Profile kit (formerly ARTseq) sequences ribosome-protected mRNA fragments to provide a snapshot of the active ribosomes in a cell.
These kits provide a simple, cost-effective solution for generating miRNA and small RNA sequencing libraries directly from total RNA, for any species.
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.
A targeted RNA sequencing panel to study cellular pathways affected by cardiotoxic compounds or stress. Assay targets cardiotoxic response markers.
Targeted RNA assays for gene expression studies: fixed or custom sequencing panels, with a simple workflow and automated data analysis.
A targeted RNA sequencing panel for studying NFκB signaling. Assays target upstream and downstream signal transduction and NFκB transcription factors.
A targeted RNA sequencing panel for studying neurodegenerative and neurotoxic pathways such as those implicated in Alzheimer’s Disease.
A targeted RNA sequencing panel for studying various stem cell types. Analyze stem cell and pluripotency markers, cytokines, growth factors, and more.
A targeted RNA sequencing panel for studying Wnt signaling. Assays upstream and downstream signal transduction genes, transcription factors, and more.
These 24-sample arrays enable economical large-scale human genotyping studies, with high-throughput processing capabilities, and the option to add up to 300K semi-custom markers.
This DNA microarray kit delivers genome-wide SNP and genetic variant information for genetic studies, especially large-scale human genotyping studies.
Infinium Exome-24 Kit arrays deliver exceptional coverage of putative functional exonic variants representing diverse populations and a range of common conditions.
GSA is a next-generation genotyping array for population-scale genetics, variant screening, and precision medicine research.
The Infinium ImmunoArray-24 v2 BeadChip is the next-generation genotyping array for detecting genetic variation in the immune system.
Robust methylation profiling microarray with unparalleled coverage of CpG islands, genes, and enhancers. Use for epigenome-wide association studies.
A cost-effective array for understanding complex disease in diverse human populations, focused on Hispanic and African American populations.
A cost-effective array for understanding complex disease in diverse human populations, focused on European, East Asian, and South Asian populations.
A cost-effective array for understanding complex disease in diverse human populations.
This 8-sample BeadChip array features ~2.5 million markers, with custom marker add-on capability, and delivers exceptional genomic coverage rates across diverse populations.
Comprehensive coverage and functional exonic content for next-generation genotyping, GWAS, and CNV analysis.
This 4-sample BeadChip array, optimized for whole-genome genotyping and CNV studies, covers > 4.3 million variants.
This BeadChip array covers > 4.3 million whole-genome variants down to 1% minor allele frequency (MAF), plus novel functional exonic variants.
This 24-sample BeadChip array offers exceptional throughput of thousands of samples per week, enabling powerful human genome-wide association studies (GWAS).
Discover novel trait and disease associations with optimized tag SNPs and functional exonic content at an attractive price.
Advance your Chinese population GWAS. This microarray provides coverage of common, intermediate, and rare variation specific to Chinese populations.
A cost-effective, high-density Illumina microarray for large-scale genetic studies focused on psychiatric predisposition and risk.
genotyping for quality control, tracking, and stratification applications including biobanking.
Infinium XT is a comprehensive microarray solution that enables production-scale genotyping of up to 50,000 single or multi-species custom variants.
Interrogate virtually any target across any species to create a fully-customized genotyping array tailored to your unique study needs.
This kit provides researchers with a comprehensive, cost-effective solution for identifying causal variants implicated in inherited cardiac conditions (ICCs).
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.
This kit removes unwanted ribosomal RNA and globin mRNA from mammalian blood RNA samples before sequencing.
Evaluate sample quality and repair degraded FFPE DNA samples for use in Infinium array-based assays.
This kit removes both cytoplasmic and mitochondrial rRNA from human, mouse, and rat samples, including partially degraded samples.
This kit removes cytoplasmic ribosomal RNA from human, mouse, or rat samples, including partially degraded samples.
Comprehensive array and next-generation sequencing solutions to accelerate research on various complex diseases.
Our targeted gene panels and microarrays can support genetic disease research by identifying causative genetic variants and chromosomal aberrations.
Find comprehensive NGS solutions for high-quality gene expression and transcriptome analysis and profiling studies.