tailieunhanh - Báo cáo sinh học: "Modeling genetic imprinting effects of DNA sequences with multilocus polymorphism data"

Tuyển tập các báo cáo nghiên cứu về sinh học được đăng trên tạp chí y học Molecular Biology cung cấp cho các bạn kiến thức về ngành sinh học đề tài: Modeling genetic imprinting effects of DNA sequences with multilocus polymorphism data. | Algorithms for Molecular Biology BioMed Central Research Modeling genetic imprinting effects of DNA sequences with multilocus polymorphism data Sheron Wen1 Chenguang Wang1 Arthur Berg1 Yao Li1 Myron M Chang2 Roger B Fillingim3 Margaret R Wallace4 Roland Staud4 Lee Kaplan4 and Rongling Wu 1 5 6 Address Department of Statistics University of Florida Gainesville Florida 32611 USA 2Department of Epidemiology and Health Policy Research University of Florida Gainesville Florida 32611 USA 3Department of Community Dentistry and Behavioral Science University of Florida Gainesville Florida 32611 USA 4Department of Molecular Genetics and Microbiology University of Florida Gainesville Florida 32611 USA 5Department of Public Health Sciences Pennsylvania State College of Medicine Hershey Pennsylvania 17033 USA and department of Statistics Pennsylvania State University University Park Pennsylvania 16802 USA Email Sheron Wen - xwen4@ Chenguang Wang - cgwang@ Arthur Berg - berg@ Yao Li - li@ Myron M Chang - mchang@ Roger B Fillingim - rfilling@ Margaret R Wallace - peggyw@ Roland Staud - staudr@ Lee Kaplan - lee@ Rongling Wu - rwu@ Corresponding author Published II August 2009 Received 4 February 2009 Algorithms for Molecular Biology 2009 4 11 doi 1748-7188-4-11 Accepted 1 1 August 2009 This article is available from http content 4 1 11 2009 Wen et al licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License http licenses by which permits unrestricted use distribution and reproduction in any medium provided the original work is properly cited. Open Access Abstract_ Single nucleotide polymorphisms SNPs represent the most widespread type of DNA sequence variation in the human genome and they have .