Machine learning based classification of cells into chronological stages using single-cell transcriptomics
Autor: | Halil I. Bilgin, Selcuk Korkmaz, Sharan Janjuha, Samata Chaudhuri, Sumeet Pal Singh, Gokmen Zararsiz, Nikolay Ninov, Sevina Dietz, Annekathrin Kränkel, Anne Eugster, Susanne Reinhardt, John E. Reid |
---|---|
Přispěvatelé: | Tıp Fakültesi |
Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
Premature aging Candidate gene Single cell transcriptomics Cytological Techniques lcsh:Medicine Biology Cycle Machine learning computer.software_genre Article Transcriptome Machine Learning 03 medical and health sciences Insulin-Secreting Cells Animals Humans lcsh:Science Zebrafish Multidisciplinary business.industry Gene Expression Profiling lcsh:R Signatures Age Factors Robustness (evolution) Sciences bio-médicales et agricoles Pancreatic-Islets biology.organism_classification Calorie intake Dynamics Gene expression profiling 030104 developmental biology lcsh:Q Biologie cellulaire Artificial intelligence Single-Cell Analysis business computer |
Zdroj: | Sci. Rep. 8:17156 (2018) Scientific Reports Scientific Reports, 8 (1 Scientific Reports, Vol 8, Iss 1, Pp 1-12 (2018) |
Popis: | Age-associated deterioration of cellular physiology leads to pathological conditions. The ability to detect premature aging could provide a window for preventive therapies against age-related diseases. However, the techniques for determining cellular age are limited, as they rely on a limited set of histological markers and lack predictive power. Here, we implement GERAS (GEnetic Reference for Age of Single-cell), a machine learning based framework capable of assigning individual cells to chronological stages based on their transcriptomes. GERAS displays greater than 90% accuracy in classifying the chronological stage of zebrafish and human pancreatic cells. The framework demonstrates robustness against biological and technical noise, as evaluated by its performance on independent samplings of single-cells. Additionally, GERAS determines the impact of differences in calorie intake and BMI on the aging of zebrafish and human pancreatic cells, respectively. We further harness the classification ability of GERAS to identify molecular factors that are potentially associated with the aging of beta-cells. We show that one of these factors, junba, is necessary to maintain the proliferative state of juvenile beta-cells. Our results showcase the applicability of a machine learning framework to classify the chronological stage of heterogeneous cell populations, while enabling detection of candidate genes associated with aging. |
Databáze: | OpenAIRE |
Externí odkaz: |