BayesMendel: an R Environment for Mendelian Risk Prediction
Gespeichert in:
Verfasser / Beitragende:
[Sining Chen, Wenyi Wang, Karl W Broman, Hormuzd A Katki, Giovanni Parmigiani]
Ort, Verlag, Jahr:
2004
Enthalten in:
Statistical Applications in Genetics and Molecular Biology, 3/1(2004-09-17), 1-19
Format:
Artikel (online)
Online Zugang:
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| 024 | 7 | 0 | |a 10.2202/1544-6115.1063 |2 doi |
| 035 | |a (NATIONALLICENCE)gruyter-10.2202/1544-6115.1063 | ||
| 245 | 0 | 0 | |a BayesMendel: an R Environment for Mendelian Risk Prediction |h [Elektronische Daten] |c [Sining Chen, Wenyi Wang, Karl W Broman, Hormuzd A Katki, Giovanni Parmigiani] |
| 520 | 3 | |a Several important syndromes are caused by deleterious germline mutations of individual genes. In both clinical and research applications it is useful to evaluate the probability that an individual carries an inherited genetic variant of these genes, and to predict the risk of disease for that individual, using information on his/her family history. Mendelian risk prediction models accomplish these goals by integrating Mendelian principles and state-of-the-art statistical models to describe phenotype/genotype relationships. Here we introduce an R library called BayesMendel that allows implementation of Mendelian models in research and counseling settings. BayesMendel is implemented in an object-oriented structure in the language R and distributed freely as an open source library. In its first release, it includes two major cancer syndromes: the breast-ovarian cancer syndrome and the hereditary non-polyposis colorectal cancer syndrome, along with up-to-date estimates of penetrance and prevalence for the corresponding genes. Input genetic parameters can be easily modified by users. BayesMendel can also serve as a generic tool for genetic epidemiologists to flexibly implement their own Mendelian models for novel syndromes and local subpopulations, without reprogramming complex statistical analyses and prediction tools. | |
| 540 | |a ©2011 Walter de Gruyter GmbH & Co. KG, Berlin/Boston | ||
| 690 | 7 | |a Genetics |2 nationallicence | |
| 690 | 7 | |a Computation |2 nationallicence | |
| 700 | 1 | |a Chen |D Sining |u The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University |4 aut | |
| 700 | 1 | |a Wang |D Wenyi |u The Johns Hopkins Bloomberg School of Public Health |4 aut | |
| 700 | 1 | |a Broman |D Karl W. |u The Johns Hopkins Bloomberg School of Public Health |4 aut | |
| 700 | 1 | |a Katki |D Hormuzd A. |u Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS |4 aut | |
| 700 | 1 | |a Parmigiani |D Giovanni |u The Sydney Kimmel Comprehensive Cancer Center, Johns Hopkins University |4 aut | |
| 773 | 0 | |t Statistical Applications in Genetics and Molecular Biology |d De Gruyter |g 3/1(2004-09-17), 1-19 |q 3:1<1 |1 2004 |2 3 |o sagmb | |
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| 908 | |D 1 |a research article |2 jats | ||
| 950 | |B NATIONALLICENCE |P 856 |E 40 |u https://doi.org/10.2202/1544-6115.1063 |q text/html |z Onlinezugriff via DOI | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Chen |D Sining |u The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Wang |D Wenyi |u The Johns Hopkins Bloomberg School of Public Health |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Broman |D Karl W. |u The Johns Hopkins Bloomberg School of Public Health |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Katki |D Hormuzd A. |u Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Parmigiani |D Giovanni |u The Sydney Kimmel Comprehensive Cancer Center, Johns Hopkins University |4 aut | ||
| 950 | |B NATIONALLICENCE |P 773 |E 0- |t Statistical Applications in Genetics and Molecular Biology |d De Gruyter |g 3/1(2004-09-17), 1-19 |q 3:1<1 |1 2004 |2 3 |o sagmb | ||
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