Patient Similarity Networks for Precision Medicine. Issue 18 (14th September 2018)
- Record Type:
- Journal Article
- Title:
- Patient Similarity Networks for Precision Medicine. Issue 18 (14th September 2018)
- Main Title:
- Patient Similarity Networks for Precision Medicine
- Authors:
- Pai, Shraddha
Bader, Gary D. - Abstract:
- Abstract: Clinical research and practice in the 21st century is poised to be transformed by analysis of computable electronic medical records and population-level genome-scale patient profiles. Genomic data capture genetic and environmental state, providing information on heterogeneity in disease and treatment outcome, but genomic-based clinical risk scores are limited. Achieving the goal of routine precision medicine that takes advantage of these rich genomics data will require computational methods that support heterogeneous data, have excellent predictive performance, and ideally, provide biologically interpretable results. Traditional machine-learning approaches excel at performance, but often have limited interpretability. Patient similarity networks are an emerging paradigm for precision medicine, in which patients are clustered or classified based on their similarities in various features, including genomic profiles. This strategy is analogous to standard medical diagnosis, has excellent performance, is interpretable, and can preserve patient privacy. We review new methods based on patient similarity networks, including Similarity Network Fusion for patient clustering and netDx for patient classification. While these methods are already useful, much work is required to improve their scalability for contemporary genetic cohorts, optimize parameters, and incorporate a wide range of genomics and clinical data. The coming 5 years will provide an opportunity to assess theAbstract: Clinical research and practice in the 21st century is poised to be transformed by analysis of computable electronic medical records and population-level genome-scale patient profiles. Genomic data capture genetic and environmental state, providing information on heterogeneity in disease and treatment outcome, but genomic-based clinical risk scores are limited. Achieving the goal of routine precision medicine that takes advantage of these rich genomics data will require computational methods that support heterogeneous data, have excellent predictive performance, and ideally, provide biologically interpretable results. Traditional machine-learning approaches excel at performance, but often have limited interpretability. Patient similarity networks are an emerging paradigm for precision medicine, in which patients are clustered or classified based on their similarities in various features, including genomic profiles. This strategy is analogous to standard medical diagnosis, has excellent performance, is interpretable, and can preserve patient privacy. We review new methods based on patient similarity networks, including Similarity Network Fusion for patient clustering and netDx for patient classification. While these methods are already useful, much work is required to improve their scalability for contemporary genetic cohorts, optimize parameters, and incorporate a wide range of genomics and clinical data. The coming 5 years will provide an opportunity to assess the utility of network-based algorithms for precision medicine. Graphical abstract: Highlights: Future clinics will combine clinical and genomic data with cellular models for precision medicine. Statistical risk calculators using genomics need to be interpretable due to small sample sizes. Patient similarity networks are a new model to integrate data to cluster/classify patients. Patient similarity networks are accurate, intuitive, preserve patient privacy, and supply mechanistic insight. … (more)
- Is Part Of:
- Journal of molecular biology. Volume 430:Issue 18(2018)Part A
- Journal:
- Journal of molecular biology
- Issue:
- Volume 430:Issue 18(2018)Part A
- Issue Display:
- Volume 430, Issue 18, Part 1 (2018)
- Year:
- 2018
- Volume:
- 430
- Issue:
- 18
- Part:
- 1
- Issue Sort Value:
- 2018-0430-0018-0001
- Page Start:
- 2924
- Page End:
- 2938
- Publication Date:
- 2018-09-14
- Subjects:
- precision medicine -- machine learning -- patient classifier -- genomics -- networks
ASCVD Atherosclerotic Cardiovascular Disease -- AUROC area under the receiver operator characteristic curve -- AUPR area under the precision–recall curve -- PSN patient similarity network -- SNF Similarity Network Fusion
Molecular biology -- Periodicals
Biology -- Periodicals
Biochemistry -- Periodicals
Bacteriology -- Periodicals
Molecular Biology -- Periodicals
Biochemistry -- Periodicals
Biologie moléculaire -- Périodiques
Biologie -- Périodiques
Biochimie -- Périodiques
Moleculaire biologie
Biochemistry
Biology
Molecular biology
Periodicals
572.805 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00222836 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.jmb.2018.05.037 ↗
- Languages:
- English
- ISSNs:
- 0022-2836
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5020.700000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 7266.xml