The 'Whole Genome Age'.
作者信息
Bugert Peter
机构信息
Institute of Transfusion Medicine and Immunology, Heidelberg University, Medical Faculty of Mannheim, Germany.
出版信息
Transfus Med Hemother. 2009;36(4):244-245. doi: 10.1159/000228919.
Abstract
摘要
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The 'Whole Genome Age'.“全基因组时代”
Transfus Med Hemother. 2009;36(4):244-245. doi: 10.1159/000228919.
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本文引用的文献
1
Whole-Genome Sequencing in Diagnostic Medicine: Too Much Information for Doctors and Patients?诊断医学中的全基因组测序：对医生和患者来说信息过多？
Transfus Med Hemother. 2009;36(4):280-281. doi: 10.1159/000228550. Epub 2009 Jul 21.
2
HLA Genotyping and Antibody Characterization Using the Luminex™ Multiplex Technology.使用Luminex™多重技术进行HLA基因分型和抗体鉴定
Transfus Med Hemother. 2009;36(4):273-278. doi: 10.1159/000228834. Epub 2009 Jul 21.
3
MALDI-TOF MS in Prenatal Genomics.产前基因组学中的基质辅助激光解吸电离飞行时间质谱技术
Transfus Med Hemother. 2009;36(4):263-272. doi: 10.1159/000223098. Epub 2009 Jun 25.
4
Technologies in the Whole-Genome Age: MALDI-TOF-Based Genotyping.全基因组时代的技术：基于基质辅助激光解吸电离飞行时间质谱的基因分型
Transfus Med Hemother. 2009;36(4):253-262. doi: 10.1159/000225089. Epub 2009 Jul 10.
5
Genome-wide Mapping of Copy Number Variations Using SNP Arrays.使用单核苷酸多态性（SNP）阵列进行全基因组拷贝数变异图谱分析。
Transfus Med Hemother. 2009;36(4):246-251. doi: 10.1159/000225372. Epub 2009 Jul 10.
6
New susceptibility locus for coronary artery disease on chromosome 3q22.3.位于3号染色体3q22.3区域的冠状动脉疾病新易感基因座。
Nat Genet. 2009 Mar;41(3):280-2. doi: 10.1038/ng.307. Epub 2009 Feb 8.
7
Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease.全基因组单倍型关联研究确定SLC22A3-LPAL2-LPA基因簇为冠状动脉疾病的一个风险位点。
Nat Genet. 2009 Mar;41(3):283-5. doi: 10.1038/ng.314. Epub 2009 Feb 8.
8
Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry for genotyping of human platelet-specific antigens.用于人类血小板特异性抗原基因分型的基质辅助激光解吸/电离飞行时间质谱分析
Transfusion. 2009 Feb;49(2):252-8. doi: 10.1111/j.1537-2995.2008.01953.x. Epub 2008 Oct 29.
9
Rapid whole-genome mutational profiling using next-generation sequencing technologies.使用下一代测序技术进行快速全基因组突变分析
Genome Res. 2008 Oct;18(10):1638-42. doi: 10.1101/gr.077776.108. Epub 2008 Sep 4.
10
A second generation human haplotype map of over 3.1 million SNPs.一张包含超过310万个单核苷酸多态性的第二代人类单倍型图谱。
Nature. 2007 Oct 18;449(7164):851-61. doi: 10.1038/nature06258.
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