New cancer stochastic models involving both hereditary and nonhereditary cancer cases: a new approach (Q355965): Difference between revisions

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Property / cites work: Stochastic modeling of carcinogenesis: state space models and estimation of parameters / rank
 
Normal rank
Property / cites work
 
Property / cites work: A stochastic two-stage carcinogenesis model: A new approach to computing the probability of observing tumor in animal bioassays / rank
 
Normal rank
Property / cites work
 
Property / cites work: A stochastic model of radiation carcinogenesis: Latent time distributions and their properties / rank
 
Normal rank
Property / cites work
 
Property / cites work: Q4230745 / rank
 
Normal rank
Property / cites work
 
Property / cites work: Q5659379 / rank
 
Normal rank
Property / cites work
 
Property / cites work: Stochastic Models with Applications to Genetics, Cancers, AIDS and Other Biomedical Systems / rank
 
Normal rank
Property / cites work
 
Property / cites work: Stochastic modeling of carcinogenesis: Some new insights / rank
 
Normal rank
Property / cites work
 
Property / cites work: Q3214142 / rank
 
Normal rank
Property / cites work
 
Property / cites work: Q4139463 / rank
 
Normal rank

Latest revision as of 16:51, 6 July 2024

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New cancer stochastic models involving both hereditary and nonhereditary cancer cases: a new approach
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    New cancer stochastic models involving both hereditary and nonhereditary cancer cases: a new approach (English)
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    25 July 2013
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    Summary: To incorporate biologically observed epidemics into multistage models of carcinogenesis, we have developed new stochastic models for human cancers. We have further incorporated genetic segregation of cancer genes into these models to derive generalized mixture models for cancer incidence. Based on these models we have developed a generalized Bayesian approach to estimate the parameters and to predict cancer incidence via Gibbs sampling procedures. We have applied these models to fit and analyze the SEER data of human eye cancers from NCI/NIH. Our results indicate that the models not only provide a logical avenue to incorporate biological information but also fit the data much better than other models. These models would not only provide more insights into human cancers but also would provide useful guidance for its prevention and control and for prediction of future cancer cases.
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