Vishnoi Anchal, Srivastava Alok, Roy Rahul, Bhattacharya Alok
Center for Computational Biology and Bioinformatics, School of Information Technology, Jawaharlal Nehru University, New Delhi 110067, India.
BMC Genomics. 2008 Aug 5;9:373. doi: 10.1186/1471-2164-9-373.
Variation in genomes among different closely-related organisms can be linked to phenotypic differences. A number of mechanisms, such as replication error, repeat expansion and contraction, recombination and transposition can contribute to genomic differences. These processes lead to generation of SNPs, different types of repeat-based and transposons or IS-element-based polymorphisms, inversions and duplications and changes in synteny. A database of all the variations in a group of organisms is not only useful for understanding genotype-phenotype relationship but also in clinical applications. There is no database available at present that provides information about detailed genomic variations among different strains and species of Mycobacterium tuberculosis complex, organisms responsible for human diseases.
MGDD is a free web-based database that allows quick user friendly search to find different types of genomic variations among a group of fully sequenced organisms belonging to M. tuberculosis complex. The searches are based on data generated by pair wise comparison using a tool that has already been described. Different types of variations that can be searched are SNPs, indels, tandem repeats and divergent regions. The searches can be designed to find specific variations either in a given gene or any given location of the query genome with respect to any other genome currently available.
Web-based database MGDD can help to find all the possible differences that exists between two strains or species of M. tuberculosis complex. The search tool is very user-friendly and can be used by anyone not familiar with computational methods and will be useful to both clinicians and researchers working on tuberculosis and other Mycobacterial diseases.
不同近缘生物体基因组中的变异可与表型差异相关联。多种机制,如复制错误、重复序列的扩增和收缩、重组及转座等,均可导致基因组差异。这些过程会引发单核苷酸多态性(SNP)的产生、不同类型基于重复序列和转座子或插入序列元件的多态性、倒位和重复以及共线性的改变。一组生物体中所有变异的数据库不仅有助于理解基因型与表型的关系,还在临床应用中具有重要价值。目前尚无数据库可提供有关结核分枝杆菌复合群不同菌株和物种间详细基因组变异的信息,而该复合群中的生物体可导致人类疾病。
MGDD是一个基于网络的免费数据库,它允许用户进行便捷的搜索,以查找结核分枝杆菌复合群中一组全基因组测序生物体间不同类型的基因组变异。搜索基于使用已描述的工具通过成对比较生成的数据。可搜索的不同类型变异包括SNP、插入缺失、串联重复和差异区域。搜索可设计为查找给定基因或查询基因组相对于当前可用的任何其他基因组的任何给定位置中的特定变异。
基于网络的数据库MGDD有助于发现结核分枝杆菌复合群两个菌株或物种之间存在的所有可能差异。该搜索工具非常用户友好,任何不熟悉计算方法的人都可使用,对从事结核病及其他分枝杆菌疾病研究的临床医生和研究人员均有用处。