• 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

Whole genome amplification and genetic analysis after extraction of proteins from dried blood spots.

作者信息

Hollegaard Mads V, Sørensen Karina M, Petersen Høgni K, Arnardottir Maria B, Nørgaard-Pedersen Bent, Thorsen Poul, Hougaard David M

出版信息

Clin Chem. 2007 Jun;53(6):1161-2. doi: 10.1373/clinchem.2006.082313.

DOI:10.1373/clinchem.2006.082313
PMID:17517589
Abstract
摘要

相似文献

1
Whole genome amplification and genetic analysis after extraction of proteins from dried blood spots.从干血斑中提取蛋白质后进行全基因组扩增和遗传分析。
Clin Chem. 2007 Jun;53(6):1161-2. doi: 10.1373/clinchem.2006.082313.
2
Genotyping whole-genome-amplified DNA from 3- to 25-year-old neonatal dried blood spot samples with reference to fresh genomic DNA.参照新鲜基因组DNA对3至25岁新生儿干血斑样本的全基因组扩增DNA进行基因分型。
Electrophoresis. 2009 Jul;30(14):2532-5. doi: 10.1002/elps.200800655.
3
Comparing whole-genome amplification methods and sources of biological samples for single-nucleotide polymorphism genotyping.比较全基因组扩增方法及用于单核苷酸多态性基因分型的生物样本来源。
Clin Chem. 2005 Aug;51(8):1520-3. doi: 10.1373/clinchem.2004.047076.
4
Genome-wide scans using archived neonatal dried blood spot samples.使用存档的新生儿干血斑样本进行全基因组扫描。
BMC Genomics. 2009 Jul 4;10:297. doi: 10.1186/1471-2164-10-297.
5
Archived neonatal dried blood spot samples can be used for accurate whole genome and exome-targeted next-generation sequencing.存档的新生儿干血斑样本可用于准确的全基因组和外显子靶向下一代测序。
Mol Genet Metab. 2013 Sep-Oct;110(1-2):65-72. doi: 10.1016/j.ymgme.2013.06.004. Epub 2013 Jun 13.
6
Accuracy of multiplexed Illumina platform-based single-nucleotide polymorphism genotyping compared between genomic and whole genome amplified DNA collected from multiple sources.比较从多个来源收集的基因组DNA和全基因组扩增DNA之间,基于Illumina多重平台的单核苷酸多态性基因分型的准确性。
Cancer Epidemiol Biomarkers Prev. 2006 Dec;15(12):2533-6. doi: 10.1158/1055-9965.EPI-06-0219.
7
Unbiased whole-genome amplification directly from clinical samples.直接从临床样本进行无偏差全基因组扩增。
Genome Res. 2003 May;13(5):954-64. doi: 10.1101/gr.816903. Epub 2003 Apr 14.
8
Use of whole genome amplification to rescue DNA from plasma samples.
Biotechniques. 2005 Oct;39(4):511-5. doi: 10.2144/000112005.
9
Combination of PURE-DNA extraction and LAMP-DNA amplification methods for accurate malaria diagnosis on dried blood spots.联合使用 PURE-DNA 提取法和 LAMP-DNA 扩增法,可提高干血斑中疟疾诊断的准确性。
Malar J. 2018 Oct 22;17(1):373. doi: 10.1186/s12936-018-2527-7.
10
Assessing quality and functionality of DNA from fresh and archival dried blood spots and recommendations for quality control guidelines.评估新鲜和存档干血斑中DNA的质量和功能以及质量控制指南建议。
Clin Chem. 2007 Aug;53(8):1401-7. doi: 10.1373/clinchem.2007.087510. Epub 2007 Jun 22.

引用本文的文献

1
The correlates of neonatal complement component 3 and 4 protein concentrations with a focus on psychiatric and autoimmune disorders.新生儿补体成分 3 和 4 蛋白浓度的相关因素及其与精神和自身免疫性疾病的关系。
Cell Genom. 2023 Dec 13;3(12):100457. doi: 10.1016/j.xgen.2023.100457.
2
Genetic correlates of vitamin D-binding protein and 25-hydroxyvitamin D in neonatal dried blood spots.新生儿干血斑中维生素 D 结合蛋白和 25-羟维生素 D 的遗传相关性。
Nat Commun. 2023 Feb 15;14(1):852. doi: 10.1038/s41467-023-36392-5.
3
Scalable, high quality, whole genome sequencing from archived, newborn, dried blood spots.
可扩展、高质量的全基因组测序,源自存档的新生儿干血斑。
NPJ Genom Med. 2023 Feb 14;8(1):5. doi: 10.1038/s41525-023-00349-w.
4
A method to correct for the influence of bovine serum albumin-associated vitamin D metabolites in protein extracts from neonatal dried blood spots.一种校正牛血清白蛋白结合的维生素 D 代谢物在新生儿干血斑蛋白提取物中影响的方法。
BMC Res Notes. 2022 Jun 3;15(1):194. doi: 10.1186/s13104-022-06077-1.
5
Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study.精神障碍患者和非精神障碍患者自杀未遂的遗传学研究:一项基于人群的全基因组关联研究。
Mol Psychiatry. 2020 Oct;25(10):2410-2421. doi: 10.1038/s41380-018-0218-y. Epub 2018 Aug 16.
6
High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA.全基因组扩增新生儿干血斑DNA的高质量外显子组测序
PLoS One. 2016 Apr 18;11(4):e0153253. doi: 10.1371/journal.pone.0153253. eCollection 2016.
7
The Danish High Risk and Resilience Study--VIA 7--a cohort study of 520 7-year-old children born of parents diagnosed with either schizophrenia, bipolar disorder or neither of these two mental disorders.丹麦高风险与复原力研究——VIA 7——一项针对520名7岁儿童的队列研究,这些儿童的父母被诊断患有精神分裂症、双相情感障碍或未患这两种精神障碍中的任何一种。
BMC Psychiatry. 2015 Oct 2;15:233. doi: 10.1186/s12888-015-0616-5.
8
High quality genome-wide genotyping from archived dried blood spots without DNA amplification.从无 DNA 扩增的存档干血斑中进行高质量的全基因组基因分型。
PLoS One. 2013 May 30;8(5):e64710. doi: 10.1371/journal.pone.0064710. Print 2013.
9
Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source.利用存档的干血斑样本作为 DNA 来源进行全基因组扫描的稳健性。
BMC Genet. 2011 Jul 4;12:58. doi: 10.1186/1471-2156-12-58.
10
Whole-genome amplified DNA from stored dried blood spots is reliable in high resolution melting curve and sequencing analysis.储存的干血斑中的全基因组扩增 DNA 可用于高分辨率熔解曲线和测序分析,结果可靠。
BMC Med Genet. 2011 Feb 9;12:22. doi: 10.1186/1471-2350-12-22.