• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

利用探针水平信息降低基因分型微阵列中的噪声。

Noise reduction from genotyping microarrays using probe level information.

作者信息

Komura Daisuke, Nishimura Kunihiro, Ishikawa Shumpei, Panda Binaya, Huang Jing, Nakamura Hiroshi, Ihara Sigeo, Hirose Michitaka, Jones Keith W, Aburatani Hiroyuki

机构信息

Dependable and High-performance Computing, Research Center for Advanced Science and Technology, University of Tokyo, 4-6-1 Komaba, Meguro-ku, Tokyo 153-8904, Japan.

出版信息

In Silico Biol. 2006;6(1-2):79-92.

PMID:16789916
Abstract

Genomic copy number change is one of the important phenomenon observed in cancer and other genetic disorders. Recently oligonucleotide microarrays have been used to analyze changes in the copy number. Although high density microarrays provide genome wide useful data on copy number, they are often associated with substantial amount of experimental noise that could affect the performance of the analyses. We used the high density oligonucleotide genotyping microarrays in our experiments that uses redundant probe tiling approach for individual SNPs. We found that the noise in the genotyping microarray data is associated with several experimental steps during target preparation and devised an algorithm that takes into account those experimental parameters. Additionally, defective probes that do not hybridize well to the target and therefore could not be modified inherently were detected and omitted automatically by using the algorithm. When we applied the algorithm to actual datasets, we could reduce the noise substantially without compressing the dynamic range. Additionally, combinatorial use of our noise reduction algorithm and conventional breakpoint detection algorithm successfully detected a microamplification of c-myc which was overlooked in the raw data. The algorithm described here is freely available with the software upon request to all non-profit researchers.

摘要

基因组拷贝数变化是在癌症和其他遗传疾病中观察到的重要现象之一。最近,寡核苷酸微阵列已被用于分析拷贝数的变化。尽管高密度微阵列提供了全基因组范围内关于拷贝数的有用数据,但它们往往伴随着大量可能影响分析性能的实验噪声。我们在实验中使用了高密度寡核苷酸基因分型微阵列,该微阵列针对单个单核苷酸多态性(SNP)采用了冗余探针平铺方法。我们发现基因分型微阵列数据中的噪声与靶标制备过程中的几个实验步骤有关,并设计了一种考虑这些实验参数的算法。此外,通过使用该算法,可以自动检测并省略那些与靶标杂交不佳、因此无法固有修饰的缺陷探针。当我们将该算法应用于实际数据集时,我们可以在不压缩动态范围的情况下大幅降低噪声。此外,我们的降噪算法与传统断点检测算法的组合使用成功检测到了原数据中被忽视的c-myc基因微扩增。应所有非营利研究人员的要求,本文所述算法可随软件免费提供。

相似文献

1
Noise reduction from genotyping microarrays using probe level information.利用探针水平信息降低基因分型微阵列中的噪声。
In Silico Biol. 2006;6(1-2):79-92.
2
A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays.一种使用高密度寡核苷酸单核苷酸多态性基因分型阵列进行拷贝数检测的强大算法。
Cancer Res. 2005 Jul 15;65(14):6071-9. doi: 10.1158/0008-5472.CAN-05-0465.
3
Allelic dosage analysis with genotyping microarrays.使用基因分型微阵列进行等位基因剂量分析。
Biochem Biophys Res Commun. 2005 Aug 12;333(4):1309-14. doi: 10.1016/j.bbrc.2005.06.040.
4
Optimal design of oligonucleotide microarrays for measurement of DNA copy-number.用于测量DNA拷贝数的寡核苷酸微阵列的优化设计。
Hum Mol Genet. 2007 Nov 15;16(22):2770-9. doi: 10.1093/hmg/ddm234. Epub 2007 Aug 28.
5
Dynamic variable selection in SNP genotype autocalling from APEX microarray data.基于APEX微阵列数据的SNP基因型自动分型中的动态变量选择
BMC Bioinformatics. 2006 Nov 30;7:521. doi: 10.1186/1471-2105-7-521.
6
PLASQ: a generalized linear model-based procedure to determine allelic dosage in cancer cells from SNP array data.PLASQ:一种基于广义线性模型的方法,用于从SNP阵列数据确定癌细胞中的等位基因剂量。
Biostatistics. 2007 Apr;8(2):323-36. doi: 10.1093/biostatistics/kxl012. Epub 2006 Jun 20.
7
Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.联合阵列比较基因组杂交和单核苷酸多态性杂合性缺失分析揭示了宫颈癌复杂的基因改变。
BMC Genomics. 2007 Feb 20;8:53. doi: 10.1186/1471-2164-8-53.
8
Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling.使用拷贝数推断工具(CNIT)和DNA池进行全基因组拷贝数分析。
Hum Mutat. 2008 Aug;29(8):1055-62. doi: 10.1002/humu.20760.
9
Copy number estimation algorithms and fluorescence in situ hybridization to describe copy number alterations in human tumors.用于描述人类肿瘤中拷贝数改变的拷贝数估计算法及荧光原位杂交技术。
Pathol Int. 2009 Apr;59(4):218-28. doi: 10.1111/j.1440-1827.2009.02354.x.
10
A multi-array multi-SNP genotyping algorithm for Affymetrix SNP microarrays.一种用于Affymetrix SNP微阵列的多阵列多SNP基因分型算法。
Bioinformatics. 2007 Jun 15;23(12):1459-67. doi: 10.1093/bioinformatics/btm131. Epub 2007 Apr 25.

引用本文的文献

1
Waved aCGH: to smooth or not to smooth.微阵列比较基因组杂交技术(aCGH):是否需要平滑处理。
Nucleic Acids Res. 2010 Apr;38(7):e94. doi: 10.1093/nar/gkp1215. Epub 2010 Jan 13.
2
Population-genetic nature of copy number variations in the human genome.人类基因组中拷贝数变异的群体遗传学性质。
Hum Mol Genet. 2010 Mar 1;19(5):761-73. doi: 10.1093/hmg/ddp541. Epub 2009 Dec 5.
3
High resolution discovery and confirmation of copy number variants in 90 Yoruba Nigerians.在 90 名约鲁巴尼日利亚人中高分辨率发现和确认拷贝数变异。
Genome Biol. 2009;10(11):R125. doi: 10.1186/gb-2009-10-11-r125. Epub 2009 Nov 9.
4
Estimating genome-wide copy number using allele-specific mixture models.使用等位基因特异性混合模型估计全基因组拷贝数。
J Comput Biol. 2008 Sep;15(7):857-66. doi: 10.1089/cmb.2007.0148.
5
Improved detection of global copy number variation using high density, non-polymorphic oligonucleotide probes.使用高密度、非多态性寡核苷酸探针改进全基因组拷贝数变异检测。
BMC Genet. 2008 Mar 28;9:27. doi: 10.1186/1471-2156-9-27.
6
Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays.使用高密度DNA寡核苷酸阵列进行全基因组人类拷贝数变异检测。
Genome Res. 2006 Dec;16(12):1575-84. doi: 10.1101/gr.5629106. Epub 2006 Nov 22.