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Trial Match

Clinical trials test new treatments — sometimes the newest options available for a disease. Find trials that are recruiting now, near you. Open one to see its eligibility rules as simple questions to go through with your doctor.

Know your stage or your test results (such as EGFR, HER2 or BRCA)? Match trials to your own profile - nothing you type is saved.

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19 recruiting trials

for Whole Exome Sequencing

Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions NCT02077894n/a1 site📍 Bethesda National Eye Institute (NEI) Identification of Clinical, Genetic and Immunological Factors Involved in the Development of Severe Bacterial Infections in Pediatrics NCT07111793NA7 sites📍 Nantes📍 Brest📍 Lyon Nantes University Hospital · Tests: Extended phenotyping, Blood sample for WES, Blood sample for PBMC freezing, POPC score evaluation, Questionnaire comple… Whole Exome Sequencing in Finding Causative Variants in Germline DNA Samples From Patients With Peripheral Neuropathy Receiving Paclitaxel for Breast Cancer NCT02610439n/a1 site📍 Boston National Cancer Institute (NCI) · Tests: Laboratory Biomarker Analysis PREcision Diagnostics in Rare genetIC Diseases and Tumors - Long Read Sequencing NCT06796751n/a1 site📍 Bologna IRCCS Azienda Ospedaliero-Universitaria di Bologna · Tests: DNA/RNA sequencing and bioinformatic data analysis Biomarkers for Diagnosis and Treatment Response in Pediatric Acute-Onset Neuropsychiatric Syndrome (PANS) NCT07718958n/a5 sites📍 Cagliari📍 Novedrate📍 Troina University of Cagliari · Tests: Psycodiagnostic evaluation, Polysomnography, 1H-NMR analysis, miRNA sequencing Whole Exome Sequencing in Finding Causative Variants in Germline DNA Samples From Patients With Hypertension Receiving Bevacizumab for Breast Cancer NCT02610413n/a1 site📍 Boston National Cancer Institute (NCI) · Tests: Laboratory Biomarker Analysis Exome and Genome Analysis to Elucidate Genetic Etiologies and Population Characteristics in the Plain Community NCT02927158n/a1 site📍 Pittsburgh University of Pittsburgh Developing a Pipeline to Employ RNA-Seq as a Complementary Diagnostic Tool in Rare Diseases NCT05996731NA1 site📍 Ranica Mario Negri Institute for Pharmacological Research · Tests: Skin biopsy Genetics of Congenital Heart Disease NCT01192048n/a1 site📍 Columbus Nationwide Children's Hospital · Tests: Blood Sample Collection Questionnaire on Congenital Cancer Signs Through Self-Assessment NCT07378423NA1 site📍 Bern Insel Gruppe AG, University Hospital Bern · Tests: Pre-Visit Preparation (PVP) Brochure, QUOCCAS Questionnaire, Germline genetic sequencing for Cancer Predisposition Synd… Prenatal Cell-free DNA Screening in Pregnancies With Diverse Genetic Risk Profiles Utilizing Targeted and Whole-exome Sequencing NCT07106853n/a2 sites📍 Hangzhou📍 Hong Kong Women's Hospital School Of Medicine Zhejiang University Genome-based Management of Patients in Precision Medicine (Ge-Med) Towards a Genomic Health Program NCT04760522NA1 site📍 Tübingen University Hospital Tuebingen · Tests: WGS Diagnostic: Blood take for genetic diagnostic The Use of Molecular Radiogenomics in Non-small Cell Lung Cancer NCT05541744n/a1 site📍 Hualien City Buddhist Tzu Chi General Hospital Whole Genome Sequencing Versus Whole Exome Sequencing for Congenital Diarrhea and Enteropahty NCT04528303NA1 site📍 Shanghai Children's Hospital of Fudan University · Tests: Whole genome sequencing, Whole exome sequencing INTERogating Cancer for Etiology, Prevention and Therapy Navigation NCT06008392n/a5 sites📍 Scottsdale📍 Jacksonville📍 Rochester Mayo Clinic · Tests: Pan-genomic Testing Whole Exome Sequencing in Finding Causative Variants in Germline DNA Samples From Patients With Congestive Heart Failure Receiving Therapy for Breast Cancer NCT02610426n/a1 site📍 Boston National Cancer Institute (NCI) · Tests: Laboratory Biomarker Analysis Whole Exome Sequencing of Familial and Pediatric Forms of Vasculitis NCT04006535n/a1 site📍 Paris Benjamin Terrier · Tests: genetic analysis Identification of Genetic Factors Implicated in Orofacial Cleft Using Whole Exome Sequencing NCT03065686NA1 site📍 Amiens Centre Hospitalier Universitaire, Amiens · Tests: identification of genetic factors Pediatric Movement Disorders of Unknown Etiology in Vietnam (VPeMD) NCT07695610n/a2 sites📍 Ho Chi Minh City📍 Ho Chi Minh City University of Medicine and Pharmacy at Ho Chi Minh City · Tests: Whole-Exome Sequencing
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