Results 21 to 30 of about 23,427,651 (311)

Haplotype analysis of APOE intragenic SNPs [PDF]

open access: yesBMC Neuroscience, 2018
APOE ε4 allele is most common genetic risk factor for Alzheimer's disease (AD) and cognitive decline. However, it remains poorly understood why only some carriers of APOE ε4 develop AD and how ethnic variabilities in APOE locus contribute to AD risk. Here, to address the role of APOE haplotypes, we reassessed the diversity of APOE locus in major ethnic
Babenko, Vladimir N.   +5 more
openaire   +4 more sources

Novel approach for deriving genome wide SNP analysis data from archived blood spots [PDF]

open access: yes, 2012
BACKGROUND: The ability to transport and store DNA at room temperature in low volumes has the advantage of optimising cost, time and storage space.
Walling, Grant A   +16 more
core   +3 more sources

Genome bioinformatic analysis of nonsynonymous SNPs [PDF]

open access: yesBMC Bioinformatics, 2007
Background: Genome-wide association studies of common diseases for common, low penetrance causal variants are underway. A proportion of these will alter protein sequences, the most common of which is the non-synonymous single nucleotide polymorphism (nsSNP).
David F. Burke   +6 more
openaire   +4 more sources

Genome-Wide Joint Meta-Analysis of SNP and SNP-by-Smoking Interaction Identifies Novel Loci for Pulmonary Function [PDF]

open access: yes, 2012
Genome-wide association studies have identified numerous genetic loci for spirometic measures of pulmonary function, forced expiratory volume in one second (FEV1), and its ratio to forced vital capacity (FEV1/FVC).
Wenbo Tang (110161)   +712 more
core   +1 more source

On the impact of relatedness on SNP association analysis [PDF]

open access: yesBMC Genetics, 2017
When testing for SNP (single nucleotide polymorphism) associations in related individuals, observations are not independent. Simple linear regression assuming independent normally distributed residuals results in an increased type I error and the power of the test is also affected in a more complicate manner.
Arnd Gross, Anke Tönjes, Markus Scholz
openaire   +3 more sources

SNPper: retrieval and analysis of human SNPs [PDF]

open access: yesBioinformatics, 2002
Abstract Motivation: Single Nucleotide Polymorphisms (SNPs) are an increasingly important tool for the study of the human genome. SNPs can be used as markers to create high-density genetic maps, as causal candidates for diseases, or to reconstruct the history of our genome.
Alberto Riva, Isaac S. Kohane
openaire   +3 more sources

A robust SNP barcode for typing Mycobacterium tuberculosis complex strains [PDF]

open access: yes, 2014
Strain-specific genomic diversity in the Mycobacterium tuberculosis complex (MTBC) is an important factor in pathogenesis that may affect virulence, transmissibility, host response and emergence of drug resistance.
Glynn, Judith R.   +29 more
core   +1 more source

Genotyping pooled DNA using 100K SNP microarrays: a step towards genomewide association scans [PDF]

open access: yes, 2006
The identification of quantitative trait loci (QTLs) of small effect size that underlie complex traits poses a particular challenge for geneticists due to the large sample sizes and large numbers of genetic markers required for genomewide association ...
Plomin, R.   +13 more
core   +1 more source

SNP-calling.txt

open access: yes, 2023
SNP 要求对 600 头腹泻仔猪进行低深度重测序。
Qi Shen (166827)
core   +1 more source

The development and characterization of a 60K SNP chip for chicken [PDF]

open access: yes, 2011
Background In livestock species like the chicken, high throughput single nucleotide polymorphism (SNP) genotyping assays are increasingly being used for whole genome association studies and as a tool in breeding (referred to as genomic selection).
Vereijken, Addie   +41 more
core   +2 more sources

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