Illumina

NCT00959504

Detection of Factor V Leiden G1691A and Factor II (Prothrombin) G20210A Point Mutations in DNA

NCT02121873

The Breast Duct: Pilot Study of Genomic Sequencing of Exfoliated Ductal Cells Obtained Through Endoscopy and Lavage

NCT01426308

Method Comparison and Clinical Specificity Study: Evaluation of the Infinium HD Cytogenetic Abnormality Test

NCT01463410

Accuracy Testing of the Chromosomal Aberration and Gene Mutation Markers of the AMLProfiler

NCT01899079

A Prospective Observational Study of Clinical Outcomes for the NanoString® Technologies Prosigna Gene Signature Assay

NCT02268786

Single Embryo TrAnsfeR of Euploid Embryo

NCT02808494

Development of a Next Generation Sequencing (NGS) -Based Assay to Detect Preeclampsia Molecular Markers

NCT03590678

Collection of Whole Blood Specimens in Pregnant Women

NCT03290469

NICUSeq: A Trial to Evaluate the Clinical Utility of Human Whole Genome Sequencing (WGS) Compared to Standard of Care in Acute Care Neonates and Infants

NCT03620110

A Study Collecting Blood Samples From Pregnant Women to Aid in the Development of a Noninvasive Prenatal Test

NCT03655223

Early Check: Expanded Screening in Newborns

NCT04170985

NeuroSeq: A Prospective Trial to Evaluate the Diagnostic Yield of Whole Genome Sequencing (WGS) in Adult Neurology

NCT04561089

Evaluation of the COVIDSeq Test in Saliva Specimens From COVID-19 Asymptomatic Illumina Personnel

NCT04561102

Evaluation of the COVIDSeq Test in Nasal Swab and Saliva From a COVID-19 Asymptomatic Population

NCT04935138

Cell-free DNA Analysis of Chromosome Anomalies in Early Pregnancy Loss

NCT05058937

A Study to Examine the Clinical Value of Comprehensive Genomic Profiling Performed by Belgian NGS Laboratories: a Belgian Precision Study of the BSMO in Collaboration With the Cancer Centre

NCT05049967

iKnow: A Prospective Study to Evaluate the Use of Multi-omics in Multi-System, Early Onset Disorders

NCT05046444

Solving Riddles Through Sequencing

NCT05372445

Microbiome and Health Indicators in People With Obesity, Prediabetes and Type 2 Diabetes Undergoing a Lifestyle Intervention

NCT05990179

Genomic Uniformed-Screening Against Rare Disease In All Newborns

NCT07201038

Ultrafast Whole Genome Sequencing for Childhood Cancer

NCT05656183

CardioSeq: Impact of WGS in Individuals With CVD

NCT05072275

Prospective Electronic Polygenic Risk Study

NCT05858268

NeuralNET Cerebral Palsy Pilot Study

NCT05175651

Prospective Electronic Polygenic Risk Study - Second Phase