原位
原位杂交
荧光
计算机科学
生物
化学
物理
光学
生物化学
基因
基因表达
有机化学
作者
Sheila J.M. O’Connor,Kathryn Turner,Sharon Barrans
出处
期刊:Methods in molecular biology
日期:2020-01-01
卷期号:: 35-70
被引量:2
标识
DOI:10.1007/978-1-0716-0623-0_3
摘要
Fluorescent in situ hybridization (FISH) techniques can be used to identify a range of chromosome abnormalities that are clinically significant in many cancers. Multicolor FISH can be used to identify multiple targets, which can be simultaneously detected in individual cells using digital imaging microscopy. In an era of precision medicine there is a requirement to make a precise diagnosis and to have a molecular classification of the tumor that can guide therapy. Cancer genomics is now regarded as a sub-specialism in pathology and genomic testing needs to be robustly integrated into the routine diagnostic practice.The FISH techniques described in this chapter have been developed over many years in a busy hematopathology diagnostic laboratory. We describe robust in-house methods for both liquid samples (blood and bone marrow mainly) and formalin-fixed paraffin-embedded (FFPE) tissue biopsies that allow for large numbers of slides to be set up in batches. The techniques described are for interphase cells in tissues where metaphase chromosome techniques are generally not applicable. Some of the FISH tests need to be carried out as an out-of-hours emergency test to make a critical diagnosis while others provide prognostic information and are used to guide downstream patient management.
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