Clinical Research Products

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24sure Microarray
Widely used microarray and proven method for accurate, timely preimplantation genetic screening results.

24sure+ Microarray
Microarray to assay whole chromosome copy number imbalances and subchromosomal structural imbalances in polar bodies, blastomeres and blastocysts.

HumanCytoSNP FFPE-12 BeadChip
This BeadChip array is optimized for cytogenetic studies using formalin-fixed paraffin-embedded (FFPE) paired tumor-normal samples.

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.

HumanKaryomap-12 DNA Analysis Kit
This genome-wide karyomapping microarray provides insight into the inheritance of single-gene defects by testing single cells from embryo biopsies.

Infinium CytoSNP-850K v1.1 BeadChip
This consortium-built array provides comprehensive coverage of cytogenetically relevant genes for congenital disorders and cancer research.

SureMDA Amplification System
Whole-genome amplification of total DNA from a single embryonic cell, or a few embryonic cells, for use in the karyomapping assay protocol.

SurePlex DNA Amplification System
Used to generate a DNA template from single cells. Ideal for use with 24sure aneuploidy screening arrays or VeriSeq PGS applications.

SureRef Reference DNA
Amplified genomic DNA recommended for use as part of the 24sure protocols when analyzing amplified DNA from a single cell or a few cells.

TruSeq Amplicon - Cancer Panel
The TruSeq Amplicon - Cancer Panel is a highly multiplexed targeted resequencing assay for detecting somatic mutations.

TruSight Cancer
This expert-defined sequencing panel targets 94 genes and 284 SNPs associated with a predisposition towards various cancers.

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

TruSight HLA v2 Sequencing Panel
Unambiguous, phase-resolved HLA typing in a single assay using proven Illumina NGS technology and Assign analysis software.

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

TruSight Myeloid Sequencing Panel
The TruSight Myeloid Sequencing Panel targets variants associated with myeloid malignancies such as AML, MDS, MPN, CML, CMML, and JMML.

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.

TruSight RNA Fusion Panel
Provides comprehensive gene fusion detection in formalin-fixed, paraffin-embedded (FFPE) and other cancer research samples.

TruSight RNA Pan-Cancer
Targeting 1385 cancer genes for gene expression, variant, and fusion detection studies in many RNA sample types including blood, bone marrow, and FFPE.

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.

TruSight Tumor 15
Focused sequencing panel to assess 15 genes that are commonly mutated in solid tumors in a single assay, with a simple, rapid workflow.

TruSight Tumor 170
Comprehensive next-generation sequencing (NGS) assay that targets DNA and RNA variants from the same FFPE sample.

TruSight Tumor 26
This targeted sequencing panel enables clinical researchers to identify low-frequency variation in solid tumors across 26 genes.

VeriSeq PGS
A fully validated next-generation sequencing solution for PGS, providing accurate results in aneuploidy screening and extending future opportunities.