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2011年医学研究热点:基因组研究认识癌症的研究动态与信息分析

已有 2275 次阅读 2011-1-19 13:43 |个人分类:信息分析|系统分类:论文交流|关键词:学者| 基因组, 托普

 
托普尔预测,基因组测序成本的降低也会给癌症研究带来好消息,“因为测序变得如此便宜、迅捷,生物信息也正变得更加先进”。拥有了这些更加迅捷的技术后,癌症研究人员将可以把病人天生的基因组和其肿瘤导致的变异基因组进行比较,以此找到导致癌症的基因。

Prediction 7: Genomics will help us understand cancer.

Topol predicted the low cost of genome sequencing will also bring good news in cancer research next year, "because the sequencing is becoming so much cheaper and fast, and because bioinformatics is getting more advanced," he said.

With faster technology, Topol said it's become increasingly feasible for cancer researchers to compare a person's genome — the "germ line" genome the patient was born with — with the mutated genome of his or her cancerous tumors, to find the genes that are driving the cancer. In other words, they’ll find the genes that are making cancerous cells act cancerous.

http://www.myhealthnewsdaily.com/seven-predicted-medical-advances-in-2011-0949/

 

genome sequencing  and   cancer research  and   bioinformatics

 http://www.gopubmed.org/web/gopubmed/WEB16OWEB10O0

 

 

信息分析报告  genome sequencing and cancer research and bioinformatics 1-19.docx

 


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