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基于蛋白质注释的牛和猪寡核苷酸阵列的开发与应用。

Development and application of bovine and porcine oligonucleotide arrays with protein-based annotation.

作者信息

Garbe John R, Elsik Christine G, Antoniou Eric, Reecy James M, Clark Karl J, Venkatraman Anand, Kim Jae-Woo, Schnabel Robert D, Michael Dickens C, Wolfinger Russell D, Fahrenkrug Scott C, Taylor Jeremy F

机构信息

Department of Animal Science, University of Minnesota, St Paul, MN 55108, USA.

出版信息

J Biomed Biotechnol. 2010;2010:453638. doi: 10.1155/2010/453638. Epub 2010 Dec 14.

Abstract

The design of oligonucleotide sequences for the detection of gene expression in species with disparate volumes of genome and EST sequence information has been broadly studied. However, a congruous strategy has yet to emerge to allow the design of sensitive and specific gene expression detection probes. This study explores the use of a phylogenomic approach to align transcribed sequences to vertebrate protein sequences for the detection of gene families to design genomewide 70-mer oligonucleotide probe sequences for bovine and porcine. The bovine array contains 23,580 probes that target the transcripts of 16,341 genes, about 72% of the total number of bovine genes. The porcine array contains 19,980 probes targeting 15,204 genes, about 76% of the genes in the Ensembl annotation of the pig genome. An initial experiment using the bovine array demonstrates the specificity and sensitivity of the array.

摘要

针对基因组和EST序列信息体量差异较大的物种,用于检测基因表达的寡核苷酸序列设计已得到广泛研究。然而,尚未出现一种统一的策略来设计灵敏且特异的基因表达检测探针。本研究探索使用系统基因组学方法,将转录序列与脊椎动物蛋白质序列进行比对,以检测基因家族,从而为牛和猪设计全基因组范围的70聚体寡核苷酸探针序列。牛基因芯片包含23,580个探针,靶向16,341个基因的转录本,约占牛基因总数的72%。猪基因芯片包含19,980个探针,靶向15,204个基因,约占猪基因组Ensembl注释中基因的76%。使用牛基因芯片进行的初步实验证明了该芯片的特异性和灵敏度。

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