Products for reproductive health research

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

Reproductive Health Products

Systems

Technology

Key Use
Clinical Research Products
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24sure Microarray

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

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24sure+ Microarray

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

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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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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.

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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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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.

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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.

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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.

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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.

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VeriSeq PGS

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