Genomics products for genetic health research

Technologies to help advance breakthroughs in genetic disease and rare disease research

Genetic Health Products

Systems

Technology

Key Use

Product Categories

Variant Class
Library Preparation Kits
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Nextera DNA Library Preparation Kit

Nextera DNA kits provide a fast and easy library prep workflow, delivering whole-genome sequencing libraries in under 90 min.

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Nextera Rapid Capture Custom Enrichment Kit

Custom target enrichment kit to rapidly interrogate those portions of the human genome most important to your specific research.

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Nextera Rapid Capture Exome and Expanded Exome Kits

Identify coding variants up to 70% faster with this exome library prep and enrichment kit. Expanded kit sequences untranslated regions (UTRs) and miRNA.

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TruSeq Custom Amplicon Low Input Kit

This library prep kit delivers sensitive and specific amplicon sequencing results from both low-input and FFPE DNA samples.

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TruSeq Custom Amplicon v1.5

Focus on key genomic regions of interest with this targeted resequencing solution, useful for very high plexity pools or longer amplicons.

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TruSeq DNA PCR-Free Library Preparation Kit

Simple, all-inclusive whole-genome sequencing (WGS) library preparation that provides accurate and comprehensive coverage of complex genomes.

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TruSeq Exome

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

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TruSeq Methyl Capture EPIC Library Prep Kit

This kit combines next-generation sequencing with epigenetic insights to accelerate biomarker discovery and understand methylation’s role in gene regulation.

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TruSeq Nano DNA Library Prep Kit

Generate whole-genome sequencing libraries and efficiently interrogate samples with limited available DNA.

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TruSeq Nano DNA Library Prep Kit for NeoPrep

DNA library preparation for use with the NeoPrep System, providing comprehensive genomic coverage with low DNA input and minimal hands-on time.

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TruSeq Rapid Exome Library Prep Kit

This exome sequencing library prep kit uses a simple, one-day workflow to provide a fast path to greater understanding of the human exome.

Microarray Kits
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Infinium Core-24 Kit

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.

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Infinium CoreExome-24 Kit

This DNA microarray kit delivers genome-wide SNP and genetic variant information for genetic studies, especially large-scale human genotyping studies.

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Infinium Exome-24 Kit

Infinium Exome-24 Kit arrays deliver exceptional coverage of putative functional exonic variants representing diverse populations and a range of common conditions.

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Infinium Global Screening Array-24 v1.0 Kit

GSA is a next-generation genotyping array for population-scale genetics, variant screening, and precision medicine research.

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Infinium Multi-Ethnic AMR/AFR-8 Kit

A cost-effective array for understanding complex disease in diverse human populations, focused on Hispanic and African American populations.

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Infinium Multi-Ethnic EUR/EAS/SAS-8 Kit

A cost-effective array for understanding complex disease in diverse human populations, focused on European, East Asian, and South Asian populations.

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Infinium Multi-Ethnic Global-8 Kit

A cost-effective array for understanding complex disease in diverse human populations.

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Infinium Omni2.5-8 Kit

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.

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Infinium Omni2.5Exome-8 Kit

Comprehensive coverage and functional exonic content for next-generation genotyping, GWAS, and CNV analysis.

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Infinium Omni5-4 Kit

This 4-sample BeadChip array, optimized for whole-genome genotyping and CNV studies, covers > 4.3 million variants.

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Infinium Omni5Exome-4 Kit

This BeadChip array covers > 4.3 million whole-genome variants down to 1% minor allele frequency (MAF), plus novel functional exonic variants.

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Infinium OmniExpress-24 Kit

This 24-sample BeadChip array offers exceptional throughput of thousands of samples per week, enabling powerful human genome-wide association studies (GWAS).

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Infinium OmniExpressExome-8 Kit

Discover novel trait and disease associations with optimized tag SNPs and functional exonic content at an attractive price.

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Infinium OmniZhongHua-8 Kit

Advance your Chinese population GWAS. This microarray provides coverage of common, intermediate, and rare variation specific to Chinese populations.

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Infinium QC Array-24 Kit

High-throughput, cost-effective genotyping for quality control, tracking, and stratification applications including biobanking.

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Infinium XT

Infinium XT is a comprehensive microarray solution that enables production-scale genotyping of up to 50,000 single or multi-species custom variants.

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Infinium iSelect HD and HTS Custom Genotyping BeadChips

Interrogate virtually any target across any species to create a fully-customized genotyping array tailored to your unique study needs.

Clinical Research Products
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HumanCytoSNP FFPE-12 BeadChip

This BeadChip array is optimized for cytogenetic studies using formalin-fixed paraffin-embedded (FFPE) paired tumor-normal samples.

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HumanCytoSNP-12 BeadChip

This 12-sample BeadChip array enables analysis of genetic and structural variation in the human genome, such as duplications, deletions, amplifications, copy-neutral LOH, and mosaicism.

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Infinium CytoSNP-850K v1.1 BeadChip

This consortium-built array provides comprehensive coverage of cytogenetically relevant genes for congenital disorders and cancer research.

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TruSight Cardio Sequencing Kit

This kit provides researchers with a comprehensive, cost-effective solution for identifying causal variants implicated in inherited cardiac conditions (ICCs).

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TruSight Inherited Disease

TruSight Inherited Disease is a targeted sequencing panel that focuses on 552 genes associated with severe, recessive pediatric onset diseases.

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TruSight One Sequencing Panel

This panel focuses on exonic regions harboring disease-causing variants. Labs can perform commonly ordered molecular assays on-site with one assay.

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TruSight Rapid Capture

TruSight Rapid Capture all-in-one kits enable targeted sequencing library preparation and enrichment for up to 96 samples in only 1.5 days.