The Marker State Space (MSS) Method for Classifying Clinical Samples

The development of accurate clinical biomarkers has been challenging in part due to the diversity between patients and diseases. One approach to account for the diversity is to use multiple markers to classify patients, based on the concept that each individual marker contributes information from it...

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Published inPloS one Vol. 8; no. 6; p. e65905
Main Authors Fallon, Brian P., Curnutte, Bryan, Maupin, Kevin A., Partyka, Katie, Choi, Sunguk, Brand, Randall E., Langmead, Christopher J., Tembe, Waibhav, Haab, Brian B.
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 04.06.2013
Public Library of Science (PLoS)
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Abstract The development of accurate clinical biomarkers has been challenging in part due to the diversity between patients and diseases. One approach to account for the diversity is to use multiple markers to classify patients, based on the concept that each individual marker contributes information from its respective subclass of patients. Here we present a new strategy for developing biomarker panels that accounts for completely distinct patient subclasses. Marker State Space (MSS) defines "marker states" based on all possible patterns of high and low values among a panel of markers. Each marker state is defined as either a case state or a control state, and a sample is classified as case or control based on the state it occupies. MSS was used to define multi-marker panels that were robust in cross validation and training-set/test-set analyses and that yielded similar classification accuracy to several other classification algorithms. A three-marker panel for discriminating pancreatic cancer patients from control subjects revealed subclasses of patients based on distinct marker states. MSS provides a straightforward approach for modeling highly divergent subclasses of patients, which may be adaptable for diverse applications.
AbstractList The development of accurate clinical biomarkers has been challenging in part due to the diversity between patients and diseases. One approach to account for the diversity is to use multiple markers to classify patients, based on the concept that each individual marker contributes information from its respective subclass of patients. Here we present a new strategy for developing biomarker panels that accounts for completely distinct patient subclasses. Marker State Space (MSS) defines "marker states" based on all possible patterns of high and low values among a panel of markers. Each marker state is defined as either a case state or a control state, and a sample is classified as case or control based on the state it occupies. MSS was used to define multi-marker panels that were robust in cross validation and training-set/test-set analyses and that yielded similar classification accuracy to several other classification algorithms. A three-marker panel for discriminating pancreatic cancer patients from control subjects revealed subclasses of patients based on distinct marker states. MSS provides a straightforward approach for modeling highly divergent subclasses of patients, which may be adaptable for diverse applications.
The development of accurate clinical biomarkers has been challenging in part due to the diversity between patients and diseases. One approach to account for the diversity is to use multiple markers to classify patients, based on the concept that each individual marker contributes information from its respective subclass of patients. Here we present a new strategy for developing biomarker panels that accounts for completely distinct patient subclasses. Marker State Space (MSS) defines "marker states" based on all possible patterns of high and low values among a panel of markers. Each marker state is defined as either a case state or a control state, and a sample is classified as case or control based on the state it occupies. MSS was used to define multi-marker panels that were robust in cross validation and training-set/test-set analyses and that yielded similar classification accuracy to several other classification algorithms. A three-marker panel for discriminating pancreatic cancer patients from control subjects revealed subclasses of patients based on distinct marker states. MSS provides a straightforward approach for modeling highly divergent subclasses of patients, which may be adaptable for diverse applications.The development of accurate clinical biomarkers has been challenging in part due to the diversity between patients and diseases. One approach to account for the diversity is to use multiple markers to classify patients, based on the concept that each individual marker contributes information from its respective subclass of patients. Here we present a new strategy for developing biomarker panels that accounts for completely distinct patient subclasses. Marker State Space (MSS) defines "marker states" based on all possible patterns of high and low values among a panel of markers. Each marker state is defined as either a case state or a control state, and a sample is classified as case or control based on the state it occupies. MSS was used to define multi-marker panels that were robust in cross validation and training-set/test-set analyses and that yielded similar classification accuracy to several other classification algorithms. A three-marker panel for discriminating pancreatic cancer patients from control subjects revealed subclasses of patients based on distinct marker states. MSS provides a straightforward approach for modeling highly divergent subclasses of patients, which may be adaptable for diverse applications.
Audience Academic
Author Maupin, Kevin A.
Langmead, Christopher J.
Brand, Randall E.
Tembe, Waibhav
Partyka, Katie
Fallon, Brian P.
Curnutte, Bryan
Choi, Sunguk
Haab, Brian B.
AuthorAffiliation 3 University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States of America
1 Laboratory of Cancer Immunodiagnostics, Van Andel Institute, Grand Rapids, Michigan, United States of America
Queen Elizabeth Hospital, Hong Kong
4 Translational Genomics Research Institute, Phoenix, Arizona, United States of America
2 Carnegie Mellon University, Pittsburgh, Pennsylvania, United States of America
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– name: 3 University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States of America
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Competing Interests: The authors have declared that no competing interests exist.
Conceived and designed the experiments: BF BC KM KP BH. Performed the experiments: BF BC KM KP. Analyzed the data: BF BC KM KP SC RB CL WT BH. Contributed reagents/materials/analysis tools: RB CL WT. Wrote the paper: BF BH.
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Snippet The development of accurate clinical biomarkers has been challenging in part due to the diversity between patients and diseases. One approach to account for...
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SubjectTerms Algorithms
Antigens
Bioindicators
Biology
Biomarkers
Biomarkers - blood
Classification
Computational Biology - methods
Diagnosis, Differential
Disease
Humans
Immunoglobulins
Laboratories
Marker panels
Medical diagnosis
Medicine
Methods
Multiculturalism & pluralism
Pancreatic cancer
Pancreatic Neoplasms - blood
Pancreatic Neoplasms - diagnosis
Patients
Prostate cancer
Proteins
Proteomics
Reproducibility of Results
Software
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Title The Marker State Space (MSS) Method for Classifying Clinical Samples
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Volume 8
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