Results 31 to 40 of about 1,500,690 (354)

Kernel-based aggregation of marker-level genetic association tests involving copy-number variation [PDF]

open access: yes, 2013
Genetic association tests involving copy-number variants (CNVs) are complicated by the fact that CNVs span multiple markers at which measurements are taken. The power of an association test at a single marker is typically low, and it is desirable to pool
Breheny, Patrick, Li, Yinglei
core   +3 more sources

Structural Variants May Be a Source of Missing Heritability in sALS

open access: yesFrontiers in Neuroscience, 2020
The underlying genetic and molecular mechanisms that drive amyotrophic lateral sclerosis (ALS) remain poorly understood. Structural variants within the genome can play a significant role in neurodegenerative disease risk, such as the repeat expansion in ...
Frances Theunissen   +25 more
doaj   +1 more source

A comparison of SNPs and microsatellites as linkage mapping markers: lessons from the zebra finch (Taeniopygia guttata) [PDF]

open access: yes, 2010
Background: Genetic linkage maps are essential tools when searching for quantitative trait loci (QTL). To maximize genome coverage and provide an evenly spaced marker distribution a combination of different types of genetic marker are sometimes used.
Ball, A.D.   +5 more
core   +3 more sources

Inflammation-associated enterotypes, host genotype, cage and inter-individual effects drive gut microbiota variation in common laboratory mice [PDF]

open access: yes, 2013
Background: Murine models are a crucial component of gut microbiome research. Unfortunately, a multitude of genetic backgrounds and experimental setups, together with inter-individual variation, complicates cross-study comparisons and a global ...
Brinkman, Brigitta   +7 more
core   +3 more sources

Genetic distance predicts trait differentiation at the subpopulation but not the individual level in eelgrass, Zostera marina. [PDF]

open access: yes, 2018
Ecological studies often assume that genetically similar individuals will be more similar in phenotypic traits, such that genetic diversity can serve as a proxy for trait diversity.
Corre V.   +6 more
core   +2 more sources

The analysis of FSH beta-subunit gene genotypes in East Anatolian Red, East Anatolian Red×Holstein, and Zavot bulls

open access: yesOpen Veterinary Science, 2021
This study aimed to investigate the genotypic distribution and population genetic parameters of the single nucleotide polymorphism (SNP) located on exon 3 at the FSHB gene in East Anatolian Red (EAR), East Anatolian Red×Holstein (EAR×H), and Zavot (Z ...
Ardicli Sena
doaj   +1 more source

Genetic Dissection of Disease Resistance to the Blue Mold Pathogen, Peronospora tabacina, in Tobacco

open access: yesAgronomy, 2015
Tobacco blue mold, caused by the obligately biotrophic oomycete pathogen Peronospora tabacina D.B. Adam, is a major foliar disease that results in significant losses in tobacco-growing areas. Natural resistance to P.
Xia Wu   +5 more
doaj   +1 more source

Modelos aleatórios na estimação da localização de QTLs em famílias de meios-irmãos Random model approach for estimation of QTL location in half-sibs families

open access: yesRevista Brasileira de Zootecnia, 2005
O procedimento de mapeamento por intervalo baseado em modelo aleatório foi aplicado para estudar sua robustez e propriedades no mapeamento de dois QTLs, em populações constituídas de famílias de meios-irmãos.
Marcos Vinicius G. Barbosa da Silva   +7 more
doaj   +1 more source

Genetic markers in oligodendroglial tumours [PDF]

open access: yesRadiology and Oncology, 2010
Oliogodendrogliomas are brain tumours composed of the cells resembling oligodendrocytes. They represent the third most common glial tumour, comprising 2.5% of all primary brain tumours and 5-20% of all gliomas.Oligodendroglial tumours with 1p and 19q loss demonstrate a better overall prognosis due to more indolent clinical behaviour and higher ...
Bunc, Gorazd   +3 more
openaire   +4 more sources

Psychosocial Outcomes in Patients With Endocrine Tumor Syndromes: A Systematic Review

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Introduction The combination of disease manifestations, the familial burden, and varying penetrance of endocrine tumor syndromes (ETSs) is unique. This review aimed to portray and summarize available data on psychosocial outcomes in patients with ETSs and explore gaps and opportunities for future research and care.
Daniël Zwerus   +6 more
wiley   +1 more source

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