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利用 1000 基因组数据集对 Affymetrix 外显子芯片中的 SNPs 进行全面调查。

Comprehensive survey of SNPs in the Affymetrix exon array using the 1000 Genomes dataset.

机构信息

Section of Genetic Medicine, Department of Medicine, The University of Chicago, Chicago, Illinois, United States of America.

出版信息

PLoS One. 2010 Feb 23;5(2):e9366. doi: 10.1371/journal.pone.0009366.

Abstract

Microarray gene expression data has been used in genome-wide association studies to allow researchers to study gene regulation as well as other complex phenotypes including disease risks and drug response. To reach scientifically sound conclusions from these studies, however, it is necessary to get reliable summarization of gene expression intensities. Among various factors that could affect expression profiling using a microarray platform, single nucleotide polymorphisms (SNPs) in target mRNA may lead to reduced signal intensity measurements and result in spurious results. The recently released 1000 Genomes Project dataset provides an opportunity to evaluate the distribution of both known and novel SNPs in the International HapMap Project lymphoblastoid cell lines (LCLs). We mapped the 1000 Genomes Project genotypic data to the Affymetrix GeneChip Human Exon 1.0ST array (exon array), which had been used in our previous studies and for which gene expression data had been made publicly available. We also evaluated the potential impact of these SNPs on the differentially spliced probesets we had identified previously. Though the 1000 Genomes Project data allowed a comprehensive survey of the SNPs in this particular array, the same approach can certainly be applied to other microarray platforms. Furthermore, we present a detailed catalogue of SNP-containing probesets (exon-level) and transcript clusters (gene-level), which can be considered in evaluating findings using the exon array as well as benefit the design of follow-up experiments and data re-analysis.

摘要

微阵列基因表达数据已被用于全基因组关联研究,使研究人员能够研究基因调控以及其他复杂表型,包括疾病风险和药物反应。然而,为了从这些研究中得出科学合理的结论,有必要对基因表达强度进行可靠的总结。在影响微阵列平台表达谱的各种因素中,靶 mRNA 中的单核苷酸多态性 (SNP) 可能导致信号强度测量值降低,并导致虚假结果。最近发布的 1000 基因组计划数据集提供了一个机会,可以评估国际人类基因组单体型图计划(HapMap Project)淋巴母细胞系(LCL)中已知和新 SNP 的分布情况。我们将 1000 基因组计划基因型数据映射到我们之前研究中使用的 Affymetrix GeneChip Human Exon 1.0ST 阵列(exon array)上,并且这些基因表达数据已经公开。我们还评估了这些 SNP 对我们之前确定的差异剪接探针集的潜在影响。尽管 1000 基因组计划数据允许对该特定阵列中的 SNP 进行全面调查,但同样的方法肯定可以应用于其他微阵列平台。此外,我们还提供了包含 SNP 的探针集(exon-level)和转录物簇(gene-level)的详细目录,这可以在评估使用 exon array 的结果时考虑,并且有助于后续实验的设计和数据重新分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a251/2826392/d12b890b463f/pone.0009366.g001.jpg

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