Takes advantage of next-generation sequencing (NGS) technology to provide comprehensive, accurate screening of all 24 chromosomes for selection of euploid embryos.
Provides in vitro fertilization (IVF) data analysis in a single framework.
Provides a comprehensive and accurate assessment of all 24 chromosomes from an embryo biopsy for preimplantation genetic screening (PGS).
We offer a comprehensive karyomapping solution for preimplantation genetic diagnosis:
For whole-genome amplification.
For microarray analysis.
Designed to improve the success of in vitro fertilization (IVF) by detecting subchromosomal imbalances in embryos of reciprocal translocation carriers.
A noninvasive prenatal test service that screens for multiple fetal chromosomal aneuploidies using a single maternal blood draw. The verifi Prenatal Test screens for T21 (Down syndrome), T18 (Edwards syndrome), and T13 (Patau syndrome).
An easy-to-use, validated CE marked IVD NIPT analysis software that removes the burden of bioinformatics development.
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.
Targets 4800 genes, enabling labs to expand and streamline their sequencing portfolio.
Focuses on researching severe, recessive pediatric onset diseases.
An FDA-cleared in vitro diagnostic (IVD) next-generation sequencing test designed to detect 139 CFTR variants.
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.
Designed by international consortia to provide the most comprehensive coverage of cytogenetically relevant genes for cancer studies.
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.
Desktop sequencer featuring a simple workflow, integrated data analysis software, and unmatched accuracy.
The first FDA-cleared platform for in vitro diagnostic (IVD) testing. It provides a research mode to generate accurate, reliable data.
The verifi Prenatal Test was developed by, and its performance characteristics were determined by Verinata Health, Inc. a wholly owned subsidiary of Illumina, Inc. The VHI laboratory is CAP-accredited and certified under the Clinical Laboratory Improvement Amendments (CLIA) as qualified to perform high complexity clinical laboratory testing. It has not been cleared or approved by the U.S. Food and Drug Administration.