Skacel Marek, Siva Ana, Xu Bo, Tubbs Raymond R
Department of Anatomic Pathology, The Cleveland Clinic Foundation, L-25, Cleveland, OH 44191, USA.
J Mol Histol. 2007 May;38(2):135-40. doi: 10.1007/s10735-006-9051-8. Epub 2006 Oct 17.
The combination of array-based comparative genomic hybridization (CGH) with fluorescence in situ hybridization utilizing custom-designed bacterial artificial chromosome (BAC) probes applied to tissue microarrays represents a powerful compendium of techniques-greatly enhancing the throughput of genomic analysis and subsequent target validation. Such approach can be automated at various levels and allows managing large volume of targets and samples in a few experiments. As such, this approach facilitates discovery, validation and implementation of findings in the process of identification of new diagnostic, prognostic and potentially therapeutic molecular markers.
基于阵列的比较基因组杂交(CGH)与利用定制设计的细菌人工染色体(BAC)探针的荧光原位杂交相结合,并应用于组织微阵列,代表了一种强大的技术组合——极大地提高了基因组分析的通量以及后续的靶点验证。这种方法可以在多个层面实现自动化,并允许在少数实验中处理大量的靶点和样本。因此,这种方法有助于在新的诊断、预后和潜在治疗分子标志物的识别过程中发现、验证和应用研究结果。