Results 21 to 30 of about 526,264 (266)

SNP interaction pattern identifier (SIPI): an intensive search for SNP–SNP interaction patterns [PDF]

open access: yesBioinformatics, 2016
Abstract Motivation Testing SNP–SNP interactions is considered as a key for overcoming bottlenecks of genetic association studies. However, related statistical methods for testing SNP–SNP interactions are underdeveloped.
Lin, Hui-Yi   +41 more
openaire   +6 more sources

Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration [PDF]

open access: yes, 2011
AIMS: To evaluate the associations of emergent genome-wide-association study-derived coronary heart disease (CHD)-associated single nucleotide polymorphisms (SNPs) with established and emerging risk factors, and the association of genome-wide-association
Angelakopoulou, A   +44 more
core   +4 more sources

Associations of IL-6 polymorphisms with Behcet's Disease in Denizli, province of Turkey

open access: yesMedicine Science, 2022
Behcet's Disease is a chronic, multisystemic disease and the etiopathogenesis of the disease develop as a result of the interaction of environmental and genetic factors. IL-6 is a proinflammatory cytokine with functions on immune response regulation
Sanem Arikan
doaj   +1 more source

SKM-SNP: SNP markers detection method

open access: yesJournal of Biomedical Informatics, 2010
SKM-SNP, SNP markers detection program, is proposed to identify a set of relevant SNPs for the association between a disease and multiple marker genotypes. We employ a subspace categorical clustering algorithm to compute a weight for each SNP in the group of patient samples and the group of normal samples, and use the weights to identify the subsets of
Liu, Y   +4 more
openaire   +4 more sources

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open access: yes, 2021
Aims. The determination of the contribution of precursor populations into the genetic structure of modern inbreds accoding to the results of DNA single nucleotide polymorphism analysis. Methods. SNP-genotyping of 5 maize inbreds with GoldenGate test, Illumina VeraCode, Sentrix array matrice, BDI-III-pannel of 384 SNP-markers, computer analysis by ...
  +6 more sources

SNP Miniplexes for Individual Identification of Random-Bred Domestic Cats. [PDF]

open access: yes, 2016
Phenotypic and genotypic characteristics of the cat can be obtained from single nucleotide polymorphisms (SNPs) analyses of fur. This study developed miniplexes using SNPs with high discriminating power for random-bred domestic cats, focusing on ...
Brooks, Ashley   +5 more
core   +2 more sources

Association between ESR1 and RBP4 genes and litter size traits in a hyperprolific line of Landrace × Large White cross sows

open access: yesVeterinární Medicína, 2019
This study was aimed at analysing single-nucleotide polymorphisms in the oestrogen receptor 1 (ESR1) and retinol-binding protein 4 (RBP4) genes in a hyperprolific line of Landrace × Large White (Topigs 20) cross sows (n = 101).
Sven Mencik   +5 more
doaj   +1 more source

SNP-Density Crossover Maps of Polymorphic Transposable Elements and HLA Genes Within MHC Class I Haplotype Blocks and Junction

open access: yesFrontiers in Genetics, 2021
The genomic region (~4 Mb) of the human major histocompatibility complex (MHC) on chromosome 6p21 is a prime model for the study and understanding of conserved polymorphic sequences (CPSs) and structural diversity of ancestral haplotypes (AHs)/conserved ...
Jerzy K. Kulski   +3 more
doaj   +1 more source

Interleukin-10 (IL-10) 1082 promoter polymorphisms and plasma IL-10 levels in patients with bacterial sepsis

open access: yesRomanian Journal of Internal Medicine, 2021
Background. Interleukin-10 (IL-10) is a multifunctional cytokine which has been seen to play a relevant role in the pathogenesis of sepsis. We examined the association between a single nucleotide polymorphism (SNP) in IL-10-1082G/A in patients with ...
Vivas Monica Chavez   +2 more
doaj   +1 more source

Characterization of the V4 and T1 polymorphism of the ADAM33 gene and its association with the development of asthma

open access: yesRevista de la Facultad de Medicina Humana, 2021
Objective: To determine the association between the presence of V4 polymorphisms of the ADAM33 gene and asthma disease and to describe the frequency of T1 polymorphism in patients from a hospital in the Lambayeque region. Materials and methods: Design of
Clarisa Carolina Arrascue Vega   +4 more
doaj   +1 more source

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