نتایج جستجو برای: genotyped individuals

تعداد نتایج: 340120  

Journal: :Journal of animal science 2015
X Guo O F Christensen T Ostersen Y Wang M S Lund G Su

A single-step method allows genetic evaluation using information of phenotypes, pedigree, and markers from genotyped and nongenotyped individuals simultaneously. This paper compared genomic predictions obtained from a single-step BLUP (SSBLUP) method, a genomic BLUP (GBLUP) method, a selection index blending (SELIND) method, and a traditional pedigree-based method (BLUP) for total number of pig...

ژورنال: Iranian Biomedical Journal 2007
Cicioglu Aridogan, Buket , Demirci, Mustafa, Kaya, Selcuk, Onal, Süleyman, Sesli Cetin, Emel ,

The aim of this study was to investigate the prevalence of hepatitis B virus (HBV) genotypes in Isparta, Southwest of Turkey, as well as the clinical features and transmission route for patients with HBV infections. Methods: Patients (n = 135) with HBV infection were included in the study. Epidemiological and clinical data were obtained. HBV genotypes were determined with a preS2 epitope ELISA ...

2014
E. Kaitlynn Allen Ani Manichaikul Wei-Min Chen Stephen S. Rich Kathleen A. Daly Michèle M. Sale

The first Genome Wide Association Study (GWAS) of otitis media (OM) found evidence of association in the Western Australian Pregnancy Cohort (Raine) study, but lacked replication in an independent OM population. The aim of this study was to investigate association at these loci in our family-based sample of chronic otitis media with effusion and recurrent otitis media (COME/ROM). Autosomal SNPs...

Journal: :American journal of human genetics 2012
Amy L Williams Nick Patterson Joseph Glessner Hakon Hakonarson David Reich

Haplotypes are an important resource for a large number of applications in human genetics, but computationally inferred haplotypes are subject to switch errors that decrease their utility. The accuracy of computationally inferred haplotypes increases with sample size, and although ever larger genotypic data sets are being generated, the fact that existing methods require substantial computation...

F. Mohamadnejad-Sangdehi, G. Rahimi-Mianji M. Gholami M. Safdari-Shahroudi S.A. Razavi-Sheshdeh

This study was performed to investigate two polymorphic sites from Cyp19 gene (PvuII and MspI) and one polymorphic site from ERα gene (SnaBI) in four cattle breeds including Mazandarani, Taleshi, Sistani and Simmental. In overall 278 samples for CYP19 and 206 samples for ERα marker sites were genotyped using polymerase chain reactionsingle-strand conformation polymorphism (PCR-RFLP) procedure. ...

Journal: :American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004
Joel Gelernter Xuexuan Liu Victor Hesselbrock Grier P Page Andrew Goddard Heping Zhang

UNLABELLED Cigarette smoking is highly destructive to individuals and society, and is moderately heritable. We completed a genomewide linkage scan to map loci increasing risk for cigarette smoking in a set of families originally identified because they segregate panic disorder (PD). One hundred forty two genotyped individuals in a total of 12 families were studied (214 subjects analyzed, includ...

2015
Zhicai She Li Li Haigang Qi Kai Song Huayong Que Guofan Zhang

BACKGROUND The Pacific oyster Crassostrea gigas is an important cultivated shellfish that is rich in nutrients. It contains high levels of glycogen, which is of high nutritional value. To investigate the genetic basis of this high glycogen content and its variation, we conducted a candidate gene association analysis using a wild population, and confirmed our results using an independent populat...

Journal: :Bioinformatics 2007
Nir Yosef Zohar Yakhini Anya Tsalenko Vessela N. Kristensen Anne-Lise Børresen-Dale Eytan Ruppin Roded Sharan

MOTIVATION Large-scale association studies, investigating the genetic determinants of a phenotype of interest, are producing increasing amounts of genomic variation data on human cohorts. A fundamental challenge in these studies is the detection of genotypic patterns that discriminate individuals exhibiting the phenotype under study from individuals that do not possess it. The difficulty stems ...

2014
August N Blackburn Angela K Dean Donna M Lehman

Whole genome sequencing (WGS) remains prohibitively expensive, which has encouraged the development of methods to impute WGS data into nonsequenced individuals using a framework of single nucleotide polymorphisms genotyped for genome-wide association studies (GWAS). Although successful methods have been developed for cohorts of unrelated individuals, current imputation methods in related indivi...

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