Abstract
Finding accurate biomarkers is key to early diagnosis and successful treatment of many otherwise incurable diseases. In this work, we study the problem of finding biomarkers through mass spectrometry (SELDI-TOF) spectra from cancerous and normal tissues. In contrast to the common practice of using vague methods such as genetic algorithms, or uninterpretable methods such as Support Vector Machines, we look for a method that is simple, intuitive, interpretable, usable, and more accurate. We introduce decision lists to this domain. Our experiments on clinical cancer datasets demonstrate that decision lists can achieve more accurate results than other methods. More interestingly, the resulting decision lists are more interpretable for possible causal relationship between cancer and differentially expressed proteins, and directly usable in clinical biomarker design. In particular, our approach is capable of finding multiple biomarkers with high sensitivity and specificity. Such a feature will provide clues for medical experts to thoroughly investigate the roles of protein in cancer development and progression. © Mary Ann Liebert, Inc.
| Original language | English |
|---|---|
| Pages (from-to) | 971-979 |
| Journal | Journal of Computational Biology |
| Volume | 12 |
| Issue number | 7 |
| DOIs | |
| Publication status | Published - Sept 2005 |
| Externally published | Yes |
Bibliographical note
Publication details (e.g. title, author(s), publication statuses and dates) are captured on an “AS IS” and “AS AVAILABLE” basis at the time of record harvesting from the data source. Suggestions for further amendments or supplementary information can be sent to [email protected].UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Research Keywords
- Biomarkers
- Cancer diagnosis
- Decision lists
- Machine learning
- Mass spectrometry
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