COLLECTION OF DNA AND RNA FROM BREAST CANCER PATIENTS
Recruiting
- Conditions
- breast cancer10006291
- Registration Number
- NL-OMON34596
- Lead Sponsor
- niversitair Medisch Centrum Sint Radboud
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 150
Inclusion Criteria
Participants have a confirmed diagnosis of breast cancer (any subtype).
Exclusion Criteria
see inclusion
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Primary outcome measures will be the generation of comprehensive catalogues of<br /><br>genomic abnormalities for a minimum<br /><br>of 500 breast cancer samples by sequencing to high coverage depth both the<br /><br>cancer and matching normal genomes<br /><br>which will include identification of single nucleotide variants, insertions,<br /><br>deletions, copy number changes, translocations<br /><br>and other chromosomal rearrangements in conjunction with the generation of<br /><br>transcriptomic and epigenomic data sets<br /><br>using state*of*the*art approaches, such that most cancer genes mutated at 3% or<br /><br>greater prevalence will be identified.</p><br>
- Secondary Outcome Measures
Name Time Method <p>none</p><br>