نتایج جستجو برای: snp array

تعداد نتایج: 154958  

2002
Marilyn Safran Irina Solomon Orit Shmueli Michal Lapidot Shai Shen-Orr Avital Adato Uri Ben-Dor Nir Esterman Naomi Rosen Inga Peter Tsviya Olender Vered Chalifa-Caspi Doron Lancet

GeneCards (http://bioinfo.weizmann.ac.il/cards/) is an automated, integrated database of human genes, genomic maps, proteins, and diseases, with software that retrieves, consolidates, searches, and displays human genome information [1, 2]. Over the past few years, the system has consistently added new features including sequence accessions, genomic locations, cDNA assemblies, orthologies, medic...

2003
ALEXANDER RENWICK PENELOPE E. BONNEN DIMITRA TRIKKA DAVID L. NELSON RANAJIT CHAKRABORTY MAREK KIMMEL

SNP sites are generally discovered by sequencing regions of the human genome in a limited number of individuals. This may leave SNP sites present in the region, but containing rare mutant nucleotides, undetected. Consequently, estimates of nucleotide diversity obtained from assays of detected SNP sites are biased. In this research we present a statistical model of the SNP discovery process, whi...

Journal: :Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing 2011
Eleftheria Zeggini Jennifer L. Asimit

There is growing interest in the role of rare variants in multifactorial disease etiology, and increasing evidence that rare variants are associated with complex traits. Single SNP tests are underpowered in rare variant association analyses, so locus-based tests must be used. Quality scores at both the SNP and genotype level are available for sequencing data and they are rarely accounted for. A...

2015
Guijie Hao Feng Lin Changkao Mu Ronghua Li Jiayun Yao Xuemei Yuan Xiaoyi Pan Jinyu Shen Chunlin Wang

Journal: :PLoS Computational Biology 2007
Rameen Beroukhim Ming Lin Yuhyun Park Ke Hao Xiaojun Zhao Levi A. Garraway Edward A. Fox Ephraim P. Hochberg Ingo K. Mellinghoff Matthias D. Hofer Aurelien Descazeaud Mark A. Rubin Matthew Meyerson Wing Hung Wong William R. Sellers Cheng Li

High-Density Oligonucleotide SNP Arrays Rameen Beroukhim, Ming Lin, Yuhyun Park, Ke Hao, Xiaojun Zhao, Levi A. Garraway, Edward A. Fox, Ephraim P. Hochberg, Ingo K. Mellinghoff, Matthias D. Hofer, Aurelien Descazeaud, Mark A. Rubin, Matthew Meyerson, Wing Hung Wong, William R. Sellers, Cheng Li doi:10.1371/journal.pcbi.0020041 In PLoS Computational Biology, volume 2, issue 5: In the subsection ...

2011
Andrés Legarra

1.1 Simple derivation of GBLUP Models for genomic selection are abundant. However, most of them rely (yet not all; [1] ) in a hierarchical formulation in which SNP markers (or haplotypes) have additive effect on the trait of interest [2]. We will focus here in models including biallelic SNP markers. Thus, n markers will have n effects, a1 ... an. Although markers have 2 alleles, a single effect...

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