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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.
This kit combines next-generation sequencing with epigenetic insights to accelerate biomarker discovery and understand methylation’s role in gene regulation.
DNA library preparation for use with the NeoPrep System, providing comprehensive genomic coverage with low DNA input and minimal hands-on time.
The TruSeq RNA Library Preparation Kits provide a simple, cost-effective solution for analysis of the coding transcriptome.
These kits provide a simple, cost-effective solution for generating miRNA and small RNA sequencing libraries directly from total RNA, for any species.
Complete view of the transcriptome with walk-away workflow, lower input requirement, and excellent reproducibility.
Targeted RNA assays for gene expression studies: custom sequencing panels with a simple workflow and automated data analysis.
GSA is a next-generation genotyping array for population-scale genetics, variant screening, and precision medicine research.
Robust methylation profiling microarray with unparalleled coverage of CpG islands, genes, and enhancers. Use for epigenome-wide association studies.
This comprehensive, high-density microarray kit enables research into cancer 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 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.
The TruSeq Amplicon - Cancer Panel is a highly multiplexed targeted resequencing assay for detecting somatic mutations.
This expert-defined sequencing panel targets 94 genes and 284 SNPs associated with a predisposition towards various cancers.
The TruSight Myeloid Sequencing Panel targets variants associated with myeloid malignancies such as AML, MDS, MPN, CML, CMML, and JMML.
Provides comprehensive gene fusion detection in formalin-fixed, paraffin-embedded (FFPE) and other cancer research samples.
Targeting 1385 cancer genes for gene expression, variant, and fusion detection studies in many RNA sample types including blood, bone marrow, and FFPE.
Focused sequencing panel to assess 15 genes that are commonly mutated in solid tumors in a single assay, with a simple, rapid workflow.
Comprehensive next-generation sequencing (NGS) assay that targets DNA and RNA variants from the same FFPE sample.
This targeted sequencing panel enables clinical researchers to identify low-frequency variation in solid tumors across 26 genes.
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.
NGS-based cancer sequencing methods provide more information in less time compared to single-gene and array-based approaches.
These assays generate target-enriched cDNA libraries from RNA, even from FFPE samples, for cancer gene fusion studies using Illumina sequencing.
Our clinical cancer research solutions deliver accurate genomic information, and enable labs to analyze multiple genes in a single test.