Bayesian approach for predicting responses to therapy from high-dimensional time-course gene expression profiles

Background: Historical and updated information provided by time-course data collected during an entire treatment period proves to be more useful than information provided by single-point data. Accurate predictions made using time-course data on multiple biomarkers that indicate a patient’s response...

Full description

Bibliographic Details
Main Authors: Fukushima, A. (Author), Hiroyasu, T. (Author), Hiwa, S. (Author), Sugimoto, M. (Author)
Format: Article
Language:English
Published: BioMed Central Ltd 2021
Subjects:
Online Access:View Fulltext in Publisher
LEADER 03256nam a2200577Ia 4500
001 10.1186-s12859-021-04052-4
008 220427s2021 CNT 000 0 und d
020 |a 14712105 (ISSN) 
245 1 0 |a Bayesian approach for predicting responses to therapy from high-dimensional time-course gene expression profiles 
260 0 |b BioMed Central Ltd  |c 2021 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1186/s12859-021-04052-4 
520 3 |a Background: Historical and updated information provided by time-course data collected during an entire treatment period proves to be more useful than information provided by single-point data. Accurate predictions made using time-course data on multiple biomarkers that indicate a patient’s response to therapy contribute positively to the decision-making process associated with designing effective treatment programs for various diseases. Therefore, the development of prediction methods incorporating time-course data on multiple markers is necessary. Results: We proposed new methods that may be used for prediction and gene selection via time-course gene expression profiles. Our prediction method consolidated multiple probabilities calculated using gene expression profiles collected over a series of time points to predict therapy response. Using two data sets collected from patients with hepatitis C virus (HCV) infection and multiple sclerosis (MS), we performed numerical experiments that predicted response to therapy and evaluated their accuracies. Our methods were more accurate than conventional methods and successfully selected genes, the functions of which were associated with the pathology of HCV infection and MS. Conclusions: The proposed method accurately predicted response to therapy using data at multiple time points. It showed higher accuracies at early time points compared to those of conventional methods. Furthermore, this method successfully selected genes that were directly associated with diseases. © 2021, The Author(s). 
650 0 4 |a Bayes theorem 
650 0 4 |a Bayes Theorem 
650 0 4 |a Bayesian 
650 0 4 |a Bayesian approaches 
650 0 4 |a Bayesian networks 
650 0 4 |a Conventional methods 
650 0 4 |a Curricula 
650 0 4 |a Decision making 
650 0 4 |a Decision making process 
650 0 4 |a Disease control 
650 0 4 |a Forecasting 
650 0 4 |a Gene expression 
650 0 4 |a Gene expression profiles 
650 0 4 |a Gene expression profiles 
650 0 4 |a genetics 
650 0 4 |a Hepacivirus 
650 0 4 |a Hepacivirus 
650 0 4 |a hepatitis C 
650 0 4 |a Hepatitis C 
650 0 4 |a human 
650 0 4 |a Humans 
650 0 4 |a Multiple biomarkers 
650 0 4 |a multiple sclerosis 
650 0 4 |a Multiple Sclerosis 
650 0 4 |a Numerical experiments 
650 0 4 |a Patient treatment 
650 0 4 |a Prediction 
650 0 4 |a Therapy response 
650 0 4 |a Time-course data 
650 0 4 |a Time-course gene expression profiles 
650 0 4 |a transcriptome 
650 0 4 |a Transcriptome 
650 0 4 |a Updated informations 
650 0 4 |a Viruses 
700 1 |a Fukushima, A.  |e author 
700 1 |a Hiroyasu, T.  |e author 
700 1 |a Hiwa, S.  |e author 
700 1 |a Sugimoto, M.  |e author 
773 |t BMC Bioinformatics