Reproductive and genetic health

Preconception and Fertility Products

Preimplantation Genetic Screening

VeriSeq PGS Kit

Takes advantage of next-generation sequencing (NGS) technology to provide comprehensive, accurate screening of all 24 chromosomes for selection of euploid embryos.

BlueFuse Multi Software

Provides in vitro fertilization (IVF) data analysis in a single framework.

24sure Microarrays

Provides a comprehensive and accurate assessment of all 24 chromosomes from an embryo biopsy for preimplantation genetic screening (PGS).

Preimplantation Genetic Diagnosis | Karyomapping Products

We offer a comprehensive karyomapping solution for preimplantation genetic diagnosis:

SureMDA Amplification System

For whole-genome amplification.

Infinium HumanKaryomap-12 DNA Analysis Kit

For microarray analysis.

NextSeq 550 System / iScan System

For scanning and imaging the HumanKaryomap BeadChip.

BlueFuse Multi Software

With karyomapping module for analysis.

Preimplantation Genetic Diagnosis | Translocation Products

24sure+ Microarray

Designed to improve the success of in vitro fertilization (IVF) by detecting subchromosomal imbalances in embryos of reciprocal translocation carriers.

Genetic Health Products

Targeted Panels

TruSight Cardio Sequencing Kit

A comprehensive, cost-effective solution for identifying causal variants implicated in inherited cardiac conditions (ICCs). It detects 174 genes related to 17 ICCs, including most cardiomyopathies and arrhythmias.

TruSight One Sequencing Panel

Targets 4800 genes, enabling labs to expand and streamline their sequencing portfolio.

TruSight Inherited Disease Panel

Focuses on researching severe, recessive pediatric onset diseases.

Cystic Fibrosis

MiSeqDx Cystic Fibrosis 139-Variant Assay

An FDA-cleared in vitro diagnostic (IVD) next-generation sequencing test designed to detect 139 CFTR variants.

MiSeqDx Cystic Fibrosis Clinical Sequencing Assay

The first FDA-cleared in vitro diagnostic (IVD) next-generation sequencing test designed to sequence all protein coding regions and intron/exon boundaries of the CFTR gene, including two large deletions, two deep intronic mutations, and indels in homopolymeric regions such as the 2184delA deletion.

Constitutional Cytogenetics

Infinium CytoSNP-850K BeadChip

Designed by international consortia to provide the most comprehensive coverage of cytogenetically relevant genes for cancer studies.

HumanCytoSNP-12 DNA Analysis BeadChip Kit

A 12-sample BeadChip array that enables analysis of genetic and structural variation in the human genome, such as duplications, deletions, amplifications, copy-neutral LOH, and mosaicism.