نتایج جستجو برای: snp array
تعداد نتایج: 154958 فیلتر نتایج به سال:
BACKGROUND To detect genes correlated with hepatocellular carcinoma (HCC), we developed a triple combination array consisting of methylation array, gene expression array and single nucleotide polymorphism (SNP) array analysis. METHODS A surgical specimen obtained from a 68-year-old female HCC patient was analyzed by triple combination array, which identified doublecortin domain-containing 2 (...
Single nucleotide polymorphisms (SNPs) are the most abundant DNA sequence variation in the genomes which can be used to associate genotypic variation to the phenotype. Therefore, availability of a high-density SNP array with uniform genome coverage can advance genetic studies and breeding applications. Here we report the development of a high-density SNP array 'Axiom_Arachis' with 58 K SNPs and...
Two high-density single nucleotide polymorphism (SNP) genotyping arrays have recently become available for bovine genomic analyses, the Illumina High-Density Bovine BeadChip Array (777,962 SNP) and the Affymetrix Axiom Genome-Wide BOS 1 Array (648,874 SNP). These products each have unique design and chemistry attributes, and the extent of marker overlap and their potential utility for quantitat...
Increasingly, biological data is being shared over the deep web. Many biological queries can only be answered by successively searching a number of distinct web-sites. This paper introduces a system that exploits parallelization for accelerating search over multiple deep web data sources. An interactive, two-stage multi-threading system is developed to achieve task parallelization, thread paral...
Accurate inference of local ancestry from whole-genome genetic variation data is critical for understanding the history of admixed human populations and detecting SNPs associated with disease via admixture mapping. Although several existing methods achieve high accuracy when inferring local ancestry for individuals resulting from the admixture of genetically distant ancestral populations (e.g.,...
UNLABELLED MAP-O-MAT is a web-based server for automated linkage mapping of human polymorphic DNA markers. MAP-O-MAT facilitates the verification of order and map distances for custom mapping sets using genotype data from the CEPH database, and from the Marshfield, SNP Consortium and Rutgers linkage maps (exclusive to the deCODE genotyping data). The CRI-MAP program is used for likelihood calcu...
Imputation of moderate-density genotypes from low-density panels is of increasing interest in genomic selection, because it can markedly reduce genotyping costs. Several imputation software packages have been developed; however, these vary in imputation accuracy and imputed genotypes may be inconsistent over methods. An AdaBoost-like approach was developed to combine imputation results from sev...
The aim of this study was to investigate influence of the NFE2L1 gene polymorphisms on some parameters of meat production in sheep. Polymorphisms of the NFE2L1 gene were detected using NimbleGen sequencing technology (Roche, USA). The effect of polymorphisms identified was investigated in Manych Merino sheep breed. In coding and regulatory parts of gene 11 single nucleotide polymorphisms (SNP) ...
Oligonucleotide arrays are used in a wide range of genomic analyses, such as gene expression profiling, comparative genomic hybridization, chromatin immunoprecipitation, SNP detection, etc. During fabrication, the sites of an oligonucleotide array are selectively exposed to light in order to activate oligonucleotides for further synthesis. Optical effects can cause unwanted illumination at mask...
نمودار تعداد نتایج جستجو در هر سال
با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید