Products for reproductive health research

Genomics technologies to deliver fast, accurate information that can guide reproductive health choices

Reproductive Health Products



Key Use
Clinical Research Products
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.

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 Inherited Disease

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

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 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.

VeriSeq PGS

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