Lawrence Livermore National Laboratory, Livermore, California, USA.
BMC Bioinformatics. 2011 Jun 16;12:240. doi: 10.1186/1471-2105-12-240.
We developed an extendable open-source Loop-mediated isothermal AMPlification (LAMP) signature design program called LAVA (LAMP Assay Versatile Analysis). LAVA was created in response to limitations of existing LAMP signature programs.
LAVA identifies combinations of six primer regions for basic LAMP signatures, or combinations of eight primer regions for LAMP signatures with loop primers, which can be used as LAMP signatures. The identified primers are conserved among target organism sequences. Primer combinations are optimized based on lengths, melting temperatures, and spacing among primer sites. We compare LAMP signature candidates for Staphylococcus aureus created both by LAVA and by PrimerExplorer. We also include signatures from a sample run targeting all strains of Mycobacterium tuberculosis.
We have designed and demonstrated new software for identifying signature candidates appropriate for LAMP assays. The software is available for download at http://lava-dna.googlecode.com/.
我们开发了一个可扩展的开源环介导等温扩增(LAMP)的签名设计程序,称为 LAVA(LAMP 分析通用分析)。LAVA 的创建是为了应对现有的 LAMP 签名程序的限制。
LAVA 可以识别基本 LAMP 签名的六个引物区域的组合,或者带有环引物的 LAMP 签名的八个引物区域的组合,这些都可以作为 LAMP 签名。鉴定出的引物在目标生物序列中是保守的。根据长度、熔点和引物位点之间的间隔来优化引物组合。我们比较了由 LAVA 和 PrimerExplorer 创建的金黄色葡萄球菌的 LAMP 签名候选物。我们还包括了针对所有结核分枝杆菌菌株的样本运行的签名。
我们已经设计并演示了用于识别适合 LAMP 检测的候选签名的新软件。该软件可在 http://lava-dna.googlecode.com/ 下载。