Abstract
We propose a new statistics for the detection of differentially expressed genes when the genes are activated only in a subset of the samples. Statistics designed for this unconventional circumstance has proved to be valuable for most cancer studies, where oncogenes are activated for a small number of disease samples. Previous efforts made in this direction include cancer outlier profile analysis (Tomlins and others, 2005), outlier sum (Tibshirani and Hastie, 2007), and outlier robust t-statistics (Wu, 2007). We propose a new statistics called maximum ordered subset t-statistics (MOST) which seems to be natural when the number of activated samples is unknown. We compare MOST to other statistics and find that the proposed method often has more power then its competitors. © The Author 2007. Published by Oxford University Press. All rights reserved.
| Original language | English |
|---|---|
| Pages (from-to) | 411-418 |
| Journal | Biostatistics |
| Volume | 9 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - Jul 2008 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Research Keywords
- Cancer
- COPA
- Differential gene expression
- Microarray
Fingerprint
Dive into the research topics of 'MOST: Detecting cancer differential gene expression'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver