Whole Genome Medical Sequencing for Genome Discovery
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|ClinicalTrials.gov Identifier: NCT01087320|
Recruitment Status : Recruiting
First Posted : March 16, 2010
Last Update Posted : December 19, 2020
- A number of rare inherited diseases affect only a few patients, and the genetic causes of these conditions remain unknown. Researchers are studying the use of a new technology called whole genome sequencing to learn which gene or genes cause these conditions. Understanding the genes that cause these diseases is important to improve diagnosis and treatment of affected patients.
- To identify the genetic cause of disorders that are difficult to identify with existing techniques.
- To develop best practices for the medical and counseling challenges of whole genome sequencing.
- Individuals who have one of the rare disorders under consideration in this study. These conditions are generally those in which the genetic cause of the disorder is unknown. The eligibility of most individual participants will be decided on a case-by-case basis by the researchers.
- Family members of affected individuals, if that family member (often a parent) may provide genetic information.
- Participants in this study will have at least one and in some cases several of the following procedures:
- A medical genetics evaluation.
- Other tests that may include x-rays, magnetic resonance imaging (MRI) exams, and consultations with other doctors. Not all studies are necessary for each person, but the information from the tests may be required to proceed with some of our gene sequencing studies.
- Clinical photographs to document certain aspects of the disorder.
- Blood and skin biopsy samples, or other tissue samples, as required by the study doctors.
- Genetic testing, as decided by the researchers. However, most participants in this study can expect to undergo whole genome sequencing, which is a technique to study all of a person s genes.
- Some participants may be asked to take part in a telephone interview and/or a web-based survey.
- Participants will have choices about what kinds of results from whole genome sequencing they wish to learn.
- After the tests have been completed and the results of the genetic studies are known, participants will be offered a return visit to the National Institutes of Health to learn these results. During this visit, participants will be asked to complete surveys and participate in interviews related to their decisions to participate in the study and to learn individual genetic test results.
|Condition or disease|
|Mental Retardation Congenital Anomaly Rare Disorders|
We aim to use genome scale medical sequencing (GSMS, to include exome and whole
genome sequencing as appropriate) to discover causative molecular lesions for a set of rare, severe phenotypes hypothesized to be caused by either somatic mutations, germline de novo heterozygous mutations, germline inherited recessive, or germline inherited dominant mutations in currently unknown or uncharacterized genes. The goal of this research is threefold: to identify causative sequence variants for disorders whose molecular etiology was previously unknown, to apply this insight to both the rare disorders under study and more common phenotypes, and to enhance the study of mutation on a genome-wide level.
We plan to recruit approximately three to six affected individuals along with both parents for each phenotype under study. Prospectively recruited trios will be brought to the NIH Clinical Center for brief clinical evaluations and molecular evaluation. Each trio will be consented to GSMS with the option to learn clinically relevant results, that is, those that explain the disorder in question (what we refer to as the primary variant ) as well as other clinically relevant findings discovered incidentally as part of the GSMS process (what we refer to as secondary variants ). Participants will be offered a return visit to NIH to learn these results.
Sequence data generated at the NIH Intramural Sequencing Center (NISC) will be screened by staff in the Biesecker laboratory for sequence variants that conform to the hypothesized inheritance pattern. All sequence variants deemed clinically relevant will be validated in a CLIA-certified laboratory and the results returned to that participant. This protocol is being designed in a way that will provide the long-term potential for pursuing many different clinical projects.
|Study Type :||Observational|
|Estimated Enrollment :||2000 participants|
|Official Title:||Whole Genome Medical Sequencing for Gene Discovery|
|Actual Study Start Date :||February 18, 2010|
Patients or family probands with genetic cause of disorders that are intractable or difficult to identify with existing technique.
- Analyze GSMS results for rare disorders for which genetic causes are known but not fully described [ Time Frame: Ongoing ]We aim to sequence penetrant cases to study the molecular variations of rare genetic disorders, to better predict pathogenicity and identify new causative variants.
- Molecular etiology of rare diseases [ Time Frame: Ongoing ]Identify the genetic cause of disorders that are intractable or difficult to identify with existing techniques, for example, disorders due tonew mutations with poor reproductive fitness though whole exome or whole genome sequencing
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01087320
|Contact: Julie Sapp||(301) email@example.com|
|Contact: Leslie G Biesecker, M.D.||(301) firstname.lastname@example.org|
|United States, Maryland|
|National Institutes of Health Clinical Center, 9000 Rockville Pike||Recruiting|
|Bethesda, Maryland, United States, 20892|
|Contact: For more information at the NIH Clinical Center contact Office of Patient Recruitment (OPR) 800-411-1222 ext TTY8664111010 email@example.com|
|Principal Investigator:||Leslie G Biesecker, M.D.||National Human Genome Research Institute (NHGRI)|