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Copy number variations (CNV) in blood and prostate cancer from prostate cancer patients.
Abstract
<p>(A) Histogram of frequency of amplification (red) or deletion (blue) of genome sequences of leukocytes (upper panel, n = 273) from prostate cancer patients. (B) Manhattan plots of p-values in association with prostate cancer recurrence of each gene CNV from leukocytes.</p- Image
- Figure
- Uncategorised
- prostate cancer outcome prediction model
- fusion transcripts
- copy number variations
- 152 CNV fragments
- sensitivity
- genome copy number analysis
- prostate cancer recurrence
- Affymetrix SNP 6.0 chip
- prediction rate
- leukocyte prediction model
- Genomic copy number variations
- specificity
- Leukocytes Predict Prostate Cancer Clinical Outcomes
- 273 prostate cancer patients
- leukocyte genomes
- prediction model
- prostate cancer patients
- prostate cancer aggressiveness
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Last time updated on 12/02/2018
This paper was published in The Francis Crick Institute.
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