Trials / Completed
CompletedNCT01108159
Integrated Whole-Genome Analysis of Hematologic Disorders
Integrated Whole-Genome Analysis of Hematologic Disorders Using High-Throughput Sequencing and Array Technologies
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 35 (actual)
- Sponsor
- Stanford University · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
We will use new technologies to look at the DNA, RNA, proteins, and metabolites in the disease-containing blood, bone marrow, or tissue and normal cells from the skin. Our goal is to analyze all of the genes in the diseased and normal skin sample. By comparing the results of the diseased sample and normal skin cells and the results of the two types of genetic information (DNA and RNA), we should be able to identify genetic changes that are important for the initiation, progression, or treatment response of that particular disorder.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Blood Draw | |
| PROCEDURE | Skin Biopsy |
Timeline
- Start date
- 2009-09-01
- Primary completion
- 2013-08-02
- Completion
- 2013-08-02
- First posted
- 2010-04-21
- Last updated
- 2018-05-31
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01108159. Inclusion in this directory is not an endorsement.