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呼吸道兔热病:以及微阵列探针设计

Respiratory Tularemia: and Microarray Probe Designing.

作者信息

Ranjbar Reza, Behzadi Payam, Mammina Caterina

机构信息

Molecular Biology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.

Department of Microbiology, College of Basic Sciences, Shahr-e-Qods Branch, Islamic Azad University, Tehran, Iran.

出版信息

Open Microbiol J. 2016 Nov 30;10:176-182. doi: 10.2174/1874285801610010176. eCollection 2016.

DOI:10.2174/1874285801610010176
PMID:28077973
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5204066/
Abstract

BACKGROUND

() is the etiological microorganism for tularemia. There are different forms of tularemia such as respiratory tularemia. Respiratory tularemia is the most severe form of tularemia with a high rate of mortality; if not treated. Therefore, traditional microbiological tools and Polymerase Chain Reaction (PCR) are not useful for a rapid, reliable, accurate, sensitive and specific diagnosis. But, DNA microarray technology does. DNA microarray technology needs to appropriate microarray probe designing.

OBJECTIVE

The main goal of this original article was to design suitable long oligo microarray probes for detection and identification of .

METHOD

For performing this research, the complete genomes of subsp. FSC198, subsp. LVS, subsp. , subsp. ( U112), and subsp. ATCC 25017 were studied NCBI BLAST tool, GView and PanSeq Servers and finally the microarray probes were produced and processed AlleleID 7.7 software and Oligoanalyzer tool, respectively.

RESULTS

In this investigation, a number of long oligo microarray probes were designed for detecting and identifying . Among these probes, 15 probes were recognized as the best candidates for microarray chip designing.

CONCLUSION

Calibrated microarray probes reduce the biasis of DNA microarray technology as an advanced, rapid, accurate and cost-effective molecular diagnostic tool with high specificity and sensitivity. Professional microarray probe designing provides us with much more facility and flexibility regarding preparation of a microarray diagnostic chip.

摘要

背景

()是兔热病的病原微生物。兔热病有不同形式,如呼吸道兔热病。呼吸道兔热病是兔热病最严重的形式,死亡率很高;若不治疗。因此,传统微生物学工具和聚合酶链反应(PCR)对于快速、可靠、准确、灵敏且特异的诊断并无用处。但是,DNA微阵列技术却有用。DNA微阵列技术需要合适的微阵列探针设计。

目的

这篇原创文章的主要目标是设计合适的长寡核苷酸微阵列探针,用于检测和鉴定()。

方法

为开展本研究,对()亚种FSC198、()亚种LVS、()亚种、()亚种(U112)和()亚种ATCC 25017的完整基因组进行了研究,分别使用NCBI BLAST工具、GView和PanSeq服务器,最后分别使用AlleleID 7.7软件和Oligoanalyzer工具制作并处理微阵列探针。

结果

在本次调查中,设计了许多用于检测和鉴定()的长寡核苷酸微阵列探针。在这些探针中,15个探针被认定为微阵列芯片设计的最佳候选探针。

结论

经过校准的微阵列探针减少了DNA微阵列技术的偏差,DNA微阵列技术是一种先进、快速、准确且经济高效的分子诊断工具,具有高特异性和高灵敏度。专业的微阵列探针设计为我们制备微阵列诊断芯片提供了更多便利和灵活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e83b/5204066/54046a1933ea/TOMICROJ-10-176_F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e83b/5204066/54046a1933ea/TOMICROJ-10-176_F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e83b/5204066/54046a1933ea/TOMICROJ-10-176_F1.jpg

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