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3
SNP Analysis and Whole Exome Sequencing: Their Application in the Analysis of a Consanguineous Pedigree Segregating Ataxia.单核苷酸多态性分析与全外显子组测序:它们在一个分离遗传性共济失调的近亲家系分析中的应用
Microarrays (Basel). 2015 Oct 23;4(4):490-502. doi: 10.3390/microarrays4040490.
4
The Role of Constitutional Copy Number Variants in Breast Cancer.体质性拷贝数变异在乳腺癌中的作用
Microarrays (Basel). 2015 Sep 8;4(3):407-23. doi: 10.3390/microarrays4030407.
5
SNPConvert: SNP Array Standardization and Integration in Livestock Species.SNPConvert:家畜物种中的SNP阵列标准化与整合
Microarrays (Basel). 2016 Jun 9;5(2):17. doi: 10.3390/microarrays5020017.
6
Identification of Critical Region Responsible for Split Hand/Foot Malformation Type 3 (SHFM3) Phenotype through Systematic Review of Literature and Mapping of Breakpoints Using Microarray Data.通过文献系统综述和利用微阵列数据绘制断点来鉴定导致3型裂手/裂足畸形(SHFM3)表型的关键区域
Microarrays (Basel). 2015 Dec 24;5(1):2. doi: 10.3390/microarrays5010002.
7
SNP Array in Hematopoietic Neoplasms: A Review.造血系统肿瘤中的单核苷酸多态性阵列:综述
Microarrays (Basel). 2015 Dec 22;5(1):1. doi: 10.3390/microarrays5010001.
8
Germ-line DNA copy number variation frequencies in a large North American population.北美一大群人中种系DNA拷贝数变异频率
Hum Genet. 2007 Nov;122(3-4):345-53. doi: 10.1007/s00439-007-0404-5. Epub 2007 Jul 19.
9
Accessing genetic information with high-density DNA arrays.使用高密度DNA阵列获取遗传信息。
Science. 1996 Oct 25;274(5287):610-4. doi: 10.1126/science.274.5287.610.

单核苷酸多态性阵列

SNP Arrays.

作者信息

Louhelainen Jari

机构信息

Pharmacy and Biomolecular Sciences, Liverpool John Moores University, James Parsons Building, Byrom Street, Liverpool L3 3AF, UK.

出版信息

Microarrays (Basel). 2016 Oct 25;5(4):27. doi: 10.3390/microarrays5040027.

DOI:10.3390/microarrays5040027
PMID:27792140
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5197946/
Abstract

The papers published in this Special Issue "SNP arrays" (Single Nucleotide Polymorphism Arrays) focus on several perspectives associated with arrays of this type. The range of papers vary from a case report to reviews, thereby targeting wider audiences working in this field. The research focus of SNP arrays is often human cancers but this Issue expands that focus to include areas such as rare conditions, animal breeding and bioinformatics tools. Given the limited scope, the spectrum of papers is nothing short of remarkable and even from a technical point of view these papers will contribute to the field at a general level. Three of the papers published in this Special Issue focus on the use of various SNP array approaches in the analysis of three different cancer types. Two of the papers concentrate on two very different rare conditions, applying the SNP arrays slightly differently. Finally, two other papers evaluate the use of the SNP arrays in the context of genetic analysis of livestock. The findings reported in these papers help to close gaps in the current literature and also to give guidelines for future applications of SNP arrays.

摘要

本期特刊“单核苷酸多态性阵列”发表的论文聚焦于与这类阵列相关的多个视角。论文范围从病例报告到综述,从而面向该领域更广泛的受众。单核苷酸多态性阵列的研究重点通常是人类癌症,但本期将这一重点扩展到包括罕见病、动物育种和生物信息学工具等领域。鉴于篇幅有限,论文的范围相当可观,而且即使从技术角度来看,这些论文也将在总体层面上为该领域做出贡献。本期特刊发表的三篇论文聚焦于使用各种单核苷酸多态性阵列方法分析三种不同类型的癌症。其中两篇论文专注于两种截然不同的罕见病,对单核苷酸多态性阵列的应用略有不同。最后,另外两篇论文评估了单核苷酸多态性阵列在牲畜遗传分析中的应用。这些论文中报告的研究结果有助于填补当前文献中的空白,并为单核苷酸多态性阵列的未来应用提供指导。