Results 11 to 20 of about 423,756 (267)

SNPs

open access: yes, 2018
VCF files containing SNPs for ground-dove Columbicola and Physconelloides. Includes SNPs for Columbicola passerinae, C. passerinae 1, C. passerinae 2, Physconelloides eurysema, and P.
Kevin Johnson (684369)   +1 more
core   +2 more sources

Improved heritability estimation from genome-wide SNPs [PDF]

open access: yes, 2012
Narrow-sense heritability (h(2)) is an important genetic parameter that quantifies the proportion of phenotypic variance in a trait attributable to the additive genetic variation generated by all causal variants.
Johnson, Michael R.   +7 more
core   +1 more source

SNPs

open access: yes, 2022
In this study, the three SNPs (rs1800686, rs3765459 and rs4810485) of CD40 gene were analyzed by multiplex polymerase chain reaction (PCR) combined with next-generation sequencing methods in 476 patients with primary cervical cancer, 744 patients with ...
Zhu (11255682)
core   +1 more source

Cross-Amplification and Validation of SNPs Conserved over 44 Million Years between Seals and Dogs [PDF]

open access: yes, 2013
Hoffman J, Thorne MAS, McEwing R, Forcada J, Ogden R. Cross-Amplification and Validation of SNPs Conserved over 44 Million Years between Seals and Dogs. PLoS ONE.
Rob Ogden (145264)   +22 more
core   +1 more source

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

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

The CYP7A1 gene rs3808607 variant is associated with susceptibility of tuberculosis in Moroccan population

open access: yesThe Pan African Medical Journal, 2014
INTRODUCTION: Despite the medical progress in treatment. Tuberculosis (TB) continues to be a serious global health problem. A genome-wide linkage study identified a major susceptibility locus on chromosomal region 8q12-q13 in Moroccan TB patients.
Mounia Qrafli   +10 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

G × EBLUP: A novel method for exploring genotype by environment interactions and genomic prediction

open access: yesFrontiers in Genetics, 2022
Genotype by environment (G × E) interaction is fundamental in the biology of complex traits and diseases. However, most of the existing methods for genomic prediction tend to ignore G × E interaction (GEI).
Hailiang Song   +3 more
doaj   +1 more source

A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia [PDF]

open access: yes, 2009
We report a genome-wide assessment of single nucleotide polymorphisms (SNPs) and copy number variants (CNVs) in schizophrenia. We investigated SNPs using 871 patients and 863 controls, following up the top hits in four independent cohorts comprising 1 ...
Rujescu, D.   +218 more
core   +1 more source

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