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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.
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.
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.
This exome sequencing library prep kit uses a simple, one-day workflow to provide a fast path to greater understanding of the human exome.
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.
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.
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 BeadChip array is optimized for cytogenetic studies using formalin-fixed paraffin-embedded (FFPE) paired tumor-normal samples.
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.
This consortium-built array provides comprehensive coverage of cytogenetically relevant genes for congenital disorders and cancer research.
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.
NGS technology can be used in rare disease research to discover causative variants of inherited disorders by assessing many genes at the same time.
We empower research into cardiomyopathy gene variant identification. Most variants associated with inherited cardiac conditions are unique familial variants.
Our cytogenetic microarrays reliably detect chromosomal imbalances of copy number and allelic contribution associated with constitutional disorders.