Multiplex Amplifiable Probe Hybridization (MAPH) Methodology as an Alternative to Comparative Genomic Hybridization (CGH)
Author:
Publisher
Humana Press
Link
http://link.springer.com/content/pdf/10.1007/978-1-60761-759-4_4
Reference24 articles.
1. Lucito, R., Nakimura, M., West, J.A., Han, Y., Chin, K., Jensen, K., et al. (1998) Genetic analysis using genomic representations. Proc. Natl. Acad. Sci. U.S.A. 95, 4487–4492.
2. Solinas-Toldo, S., Lampel, S., Stilgenbauer, S., Nickolenko, J., Benner, A., Döhner, H., et al. (1997) Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances. Genes Chromosomes Cancer 20, 399–407.
3. Wagenstaller, J., Spranger, S., Lorenz-Depiereux, B., Kazmierczak, B., Nathrath, M., Wahl, D., et al. (2007) Copy-number variations measured by single-nucleotide-polymorphism oligonucleotide arrays in patients with mental retardation. Am. J. Hum. Genet. 81, 768–779.
4. Bignell, G.R., Huang, J., Greshock, J., Watt, S., Butler, A., West, S., et al. (2004) High-resolution analysis of DNA copy number using oligonucleotide microarrays. Genome Res. 14, 287–295.
5. Patsalis, P.C., Kousoulidou, L., Männik, K., Sismani, C., Zilina, O., Parkel, S., et al. (2007) Detection of small genomic imbalances using microarray-based multiplex amplifiable probe hybridization. Eur. J. Hum. Genet. 15, 162–172.
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. AhRR and PPP1R3C: Potential Prognostic Biomarkers for Serous Ovarian Cancer;International Journal of Molecular Sciences;2023-07-14
2. Accurate clinical detection of exon copy number variants in a targeted NGS panel using DECoN;Wellcome Open Research;2016-11-25
3. Comprehensive Screening of Gene Copy Number Aberrations in Formalin-Fixed, Paraffin-Embedded Solid Tumors Using Molecular Inversion Probe–Based Single-Nucleotide Polymorphism Array;The Journal of Molecular Diagnostics;2016-09
4. Detection of large gene rearrangements in X-linked genes by dosage analysis: identification of novel α-galactosidase A (GLA) deletions causing Fabry disease;Human Mutation;2011-03-29
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3