首页> 外文会议>Pacific Symposium on Biocomputing >CANCER PANOMICS: COMPUTATIONAL METHODS AND INFRASTRUCTURE FOR INTEGRATIVE ANALYSIS OF CANCER HIGH-THROUGHPUT “OMICS'DATA
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CANCER PANOMICS: COMPUTATIONAL METHODS AND INFRASTRUCTURE FOR INTEGRATIVE ANALYSIS OF CANCER HIGH-THROUGHPUT “OMICS'DATA

机译:癌症PloMics:癌症高吞吐量“OMIC”数据综合分析的计算方法和基础设施

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Targeted cancer treatment is becoming the goal of newly developed oncology medicines and has already shown promise in some spectacular cases such as the case of BRAF kinase inhibitors in BRAF-mutant (e.g. V600E) melanoma.1 These developments are driven by the advent of high-throughput sequencing, which continues to drop in cost, and that has enabled the sequencing of the genome, transcriptome, and epigenome of the tumors of a large number of cancer patients in order to discover the molecular aberrations that drive the oncogenesis of several types of cancer.2 Applying these technologies in the clinic promises to transform cancer treatment by identifying therapeutic vulnerabilities of each patient tumor.3 These approaches will need to address the panomics of cancer - the integration of the complex combination of patient-specific characteristics that drive the development of each person's tumor and response to therapy. This in turn necessitates new computational methods to integrate large-scale "omics" data for each patient with their electronic medical records, and in the context of the results from large-scale pan-cancer research studies, to select the best therapy and/or clinical trial for the patient at hand.
机译:目标癌症治疗正在成为新开发的肿瘤医学的目标,并且已经在一些壮观的病例中显示出许可,例如BRAF-突变体(例如V600E)黑色素瘤中BRAF激酶抑制剂的情况.1这些发展是由高度的出现驱动的通量测序,继续在成本下降,并启用了基因组,转录组测序和表观大量癌症患者的肿瘤,以发现驱动几种类型的癌症的肿瘤发生的分子畸变.2在诊所应用这些技术,通过鉴定每患者肿瘤的治疗性脆弱性,将这些技术转化为转化癌症治疗.3这些方法需要解决癌症的全面形态 - 患者特异性特征的复杂组合的整合每个人的肿瘤和治疗的反应。这反过来需要新的计算方法,为每位患者集成大规模的“OMIC”数据,以其电子医疗记录,以及大规模泛癌研究研究的结果,选择最佳治疗和/或手头患者的临床试验。

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