about
The case for selection at CCR5-Delta32Gene losses during human originsSingle nucleotide polymorphism-based validation of exonic splicing enhancersGenetic variation in an individual human exomeCurrent limitations of SNP data from the public domain for studies of complex disorders: a test for ten candidate genes for obesity and osteoporosisA high-density admixture map for disease gene discovery in african americansSingle nucleotide differences (SNDs) in the dbSNP database may lead to errors in genotyping and haplotyping studiesThe SNPlex genotyping system: a flexible and scalable platform for SNP genotypingNew methods for finding disease-susceptibility genes: impact and potentialTarget SNP selection in complex disease association studiesCharacterisation of the genomic architecture of human chromosome 17q and evaluation of different methods for haplotype block definitionAdvanced sequencing technologies: methods and goalsComputational approaches to study the effects of small genomic variations.Effective screening of informative single nucleotide polymorphisms using the novel method of restriction fragment mass polymorphism.Large-scale validation of single nucleotide polymorphisms in gene regionsA new model calling procedure for Illumina BeadArray data.Automated SNP detection from a large collection of white spruce expressed sequences: contributing factors and approaches for the categorization of SNPsLarge-scale inference of the point mutational spectrum in human segmental duplicationsSingle nucleotide variation analysis in 65 candidate genes for CNS disorders in a representative sample of the European population.Human microRNA oncogenes and tumor suppressors show significantly different biological patterns: from functions to targets.Functionally distinct polymorphic sequences in the human genome that are targets for p53 transactivation.Genome-wide association studies in cancer--current and future directionsProspects for identifying functional variation across the genomeHaplotype diversity across 100 candidate genes for inflammation, lipid metabolism, and blood pressure regulation in two populationsJumping on the Train of Personalized Medicine: A Primer for Non-Geneticist Clinicians: Part 1. Fundamental Concepts in Molecular Genetics.M(3): an improved SNP calling algorithm for Illumina BeadArray dataAllelic spectrum of the natural variation in CRP.Comprehensive association testing of common mitochondrial DNA variation in metabolic disease.Strong association of socioeconomic status with genetic ancestry in Latinos: implications for admixture studies of type 2 diabetesM(3)-S: a genotype calling method incorporating information from samples with known genotypes.Optimal selection of SNP markers for disease association studies.The two single nucleotide polymorphisms in the H37/RBM5 tumour suppressor gene at 3p21.3 correlated with different subtypes of non-small cell lung cancers.Microarrays in veterinary diagnostics.An information-driven approach to pharmacogenomics.SNPs at miR-155 binding sites of TYRP1 explain discrepancy between mRNA and protein and refine TYRP1 prognostic value in melanoma.Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms.Development and Validation of Single Nucleotide Polymorphisms (SNPs) Markers from Two Transcriptome 454-Runs of Turbot (Scophthalmus maximus) Using High-Throughput Genotyping.Inflammatory bowel disease: genetic and epidemiologic considerationsHigh fidelity of whole-genome amplified DNA on high-density single nucleotide polymorphism arraysHaplotype analysis of the apolipoprotein gene cluster on human chromosome 11.
P2860
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P2860
description
2003 nî lūn-bûn
@nan
2003 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի մարտին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Quality and completeness of SNP databases.
@ast
Quality and completeness of SNP databases.
@en
Quality and completeness of SNP databases.
@nl
type
label
Quality and completeness of SNP databases.
@ast
Quality and completeness of SNP databases.
@en
Quality and completeness of SNP databases.
@nl
prefLabel
Quality and completeness of SNP databases.
@ast
Quality and completeness of SNP databases.
@en
Quality and completeness of SNP databases.
@nl
P356
P1433
P1476
Quality and completeness of SNP databases.
@en
P2093
David E Reich
P2888
P304
P356
10.1038/NG1133
P407
P577
2003-03-24T00:00:00Z