[PDF] Top 20 Blocking approach for identification of rare variants in family-based association studies.
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Blocking approach for identification of rare variants in family-based association studies.
... or family-based sampling designs to study the genetic basis of complex ...proposed in the literature for detecting rare variant associations, including those discussed above, are for ... See full document
11
A novel support vector machine-based approach for rare variant detection.
... common variants (CVs) that contribute to complex genetic diseases have been successfully identified from genome- wide association studies (GWAS), only a portion of heritability is explained by ... See full document
9
Differing roles for TCF4 and COL8A2 in central corneal thickness and fuchs endothelial corneal dystrophy.
... frequencies in FECD cases and controls were estimated by the maximum-likelihood approach for family data implement- ed in the FREQ program in the ...[49]. Association analysis ... See full document
10
Reconsidering association testing methods using single-variant test statistics as alternatives to pooling tests for sequence data with rare variants.
... those of the original studies [5,6] suggesting that the CMC and WSS tests were superior to locus- wide inference using nonnegative single-variant test ...these studies in two important ways ... See full document
15
Population-specific haplotype association of the postsynaptic density gene DLG4 with schizophrenia, in family-based association studies.
... genomic variants of genes encoding postsynaptic density proteins, 31 SNPs from four genes (DLG4, DLG1, PICK1 and MDM2) were queried in schizophrenia pedigrees of Japanese ...located in ... See full document
8
Detecting rare variants in case-parents association studies.
... use of a random-effects model. The p-values of the four tests are computed using a permutation ...this approach, we only need genotype data of the variants for computing the four test ... See full document
9
Family Business Field Lab JOÃO PEDRO AZEVEDO TEIXEIRA GUEDES MONTEIRO
... semester of 2015 had just started and Ach Brito´s results in the last 10 years were admirable taking into account the macroeconomic context and, particularly, the situation in Portugal since the ... See full document
28
Rev. Saúde Pública vol.43 número3
... category of “interdisciplinarity,” un- derstood as an interactive attitude of multiple areas of knowledge in the light of the individual’s inability to respond to complex problems, ... See full document
8
A HuGE Review and Meta-Analyses of Genetic Associations in New Onset Diabetes after Kidney Transplantation.
... between studies. There were a small number of studies available for many of the variants; larger, carefully phenotyped studies would provide better power to identify alleles ... See full document
13
Chitinolytic Bacteria Isolated from Chili Rhizosphere: Chitinase Characterization and Its Application as Biocontrol for Whitefly (<i>Bemisia tabaci</i> Genn.)
... ability of cell culture and chitinases of I.5 and I.21 isolates in degrading exoskeleton of whitefly (Bemisia ...level of exoskeleton caused by the treatment was ...chitin of the ... See full document
6
The application of optical measurements for the determination of accuracy of gear wheels casts manufactured in the RT/RP process
... Before taking the measurements, an anti-reflection coating was applied on the tested gear wheel. The thickness of the coating ranged from 0,8 µm do 1,2 µm. The measurements were taken at the Institute of ... See full document
4
Association between 5p12 genomic markers and breast cancer susceptibility: evidence from 19 case-control studies.
... variations in 5p12 influences BC risk remains ...are in a region of high LD as reported by Stacey et al ...gene in this ...component of the small subunit of the mitochondrial ... See full document
8
Assessing methods for assigning SNPs to genes in gene-based tests of association using common variants.
... imputed in GWAS as an alternative to single-marker ...causal variants will improve power and reduce multiple testing penalties, these methods have generally performed poorly in ...practice. In ... See full document
9
Model Based Approach for Identification of Gears and Bearings Failure Modes
... errors of the gear ...appear in each complete ...harmonics in the spectrum. The removal of the regular gear meshing harmonics (residual part) sometimes with their low-order sidebands ... See full document
10
Identification and selection of studies
... review of the literature, which does not require Ethics Committee in Research approval, but is being analyzed by the International P r o s p e c t i v e R e g i s t e r o f S y s t e m a t i c R e v i e w s ... See full document
8
A method to prioritize quantitative traits and individuals for sequencing in family-based studies.
... advances in DNA sequencing, it is now technically feasible to evaluate the contribution of rare variation to complex traits and ...exome) of all individuals in each ...individuals ... See full document
9
Barriers And Profits Of Distan ce Education In Operations Research Based Decision Analysis
... is based on the following rules: (1) the rule of small steps – teaching material should be divided into small pieces – teaching frames; (2) the rule of an immediate confirmation of an answer – ... See full document
12
Bayesian detection of causal rare variants under posterior consistency.
... pooled association testing (EMMPAT) method [11], hierarchical generalized linear model (HGLM) method [12,13], and Bayesian risk index (BRI) method ...an association set of ...all variants with ... See full document
16
Alternative parameterizations of relatedness in whole genome association analysis of pre-weaning traits of Nelore-Angus calves
... taurus studies were 35, 91, and 339 (Snelling et ...jority of detected loci (30 of 31) were from ...proportion of phenotypic variance accounted for by each SNP (singly, that is, not in ... See full document
8
Study of USH1 splicing variants through minigenes and transcript analysis from nasal epithelial cells.
... purpose of this study was to determine the pathologic nature of eighteen USH1 putative splicing variants found in our series and their effect in the splicing process by minigene ... See full document
11
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