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Fluorescence in situ hybridization (FISH): An increasingly demanded tool for biomarker research and personalized medicine
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Journal of Molecular Biomarkers & Diagnosis

ISSN: 2155-9929

Open Access

Fluorescence in situ hybridization (FISH): An increasingly demanded tool for biomarker research and personalized medicine


7th International Conference and Expo on Molecular & Cancer Biomarkers

September 15-16, 2016 Berlin, Germany

Weimin Miao

Chinese Academy of Medical Sciences and Peking Union Medical College, China

Scientific Tracks Abstracts: J Mol Biomark Diagn

Abstract :

Extensive studies conducted over the last two decades have identified recurrent genomic abnormalities as potential driving factors underlying a variety of cancers. With respect to biomarker detection, a series of innovative high-throughput molecular tests, such as array-based comparative genome hybridization (aCGH), single nucleotide polymorphism (SNP) arrays and next generation sequencing, have recently been developed and incorporated into routine clinical practice. However, although it is a classical low-throughput cytogenetic test, fluorescence in situ hybridization (FISH) does not show signs of fading; on the contrary, it plays an increasingly important role in detecting specific biomarkers in solid and hematologic neoplasms and has therefore become an indispensable part of the rapidly developing field of personalized medicine. For example, FISH has become gold standards for detecting cancer biomarkers, such as BCR-ABL1, PML-Rara, Her-2, EML4-ALK, BRAF, ROS1 and FGFR. Many of these FISH assays are actually the companion diagnostic tests directly involved in the targeted therapies and personalized medicine. Furthermore, FISH, especially quntitative multi-gene FISH has been increasingly used for molecular pathology subtyping, disease stratification, therapeutic guidance and prognosis evaluation. In this talk, I will summariz recent advances in FISH application for both de novo discovery and routine diagnosis for chromosomal rearrangements and amplification or deletion of genomic components that are associated with the pathogenesis of various hematopoietic and nonhematopoietic malignancies. I will also briefly review the recent developments in FISH methodology. Finally, I will introduce a new methodology-sequential FISH that we have developed recently for multi-gene analysis at the single-cell level.

Biography :

Weimin Miao has obtained the Medical degree from Shanghai Second Military Medical Univeristy and has completed his PhD from Fudan University in China. He did his Post-doctoral studies from Harvard Medical School in US and McGill Univeristy in Canada. He used to work as an Assistant Professor in Univeristy of Tennessee. Currently, he is Professor of Chinese Academy of Medical Sciences and Peking Union Medical College, a top medical research organization. He has published more than 50 papers in reputed journals. He also served as a Chief Scientist in VCANBIO company, developing advanced molecular diagnostic products for clinical use.

Email: miaowm@hotmail.com

Google Scholar citation report
Citations: 2054

Journal of Molecular Biomarkers & Diagnosis received 2054 citations as per Google Scholar report

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