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首页> 外文期刊>Journal of proteomics >Detection and verification of 2.3 million cancer mutations in NCI60 cancer cell lines with a cloud search engine
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Detection and verification of 2.3 million cancer mutations in NCI60 cancer cell lines with a cloud search engine

机译:用云搜索引擎检测和验证NCI60癌细胞系中的230万癌突变

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Today we have unprecedented access to human genomic and proteomic data that appear to be rapidly approaching our current understanding of comprehensive coverage. Combining genomic information with shotgun proteomics remains challenging due to the large increase in proteomics search space. However, making this connection between genomic and proteomic information is critical for cancer studies to vaccine development. Furthermore, as we progress towards personalized medicine, it will be essential for proteomics analysis to identify individual mutations and variants in order to fully understand protein networks and to develop personalized therapies. While these advantages are well-established, only a few studies have demonstrated the successful integration of proteomic data with large genomic input. We present and examine the abilities of Bolt, a new cloud-based proteomics search engine to search for the presence of over 2.3 million known cancer mutations in a matter of minutes while still performing a standard proteomics search that includes 31 post translational modifications. We use previously published proteomics data sets and identify mutations that are verified using genomic studies as well as previous proteomics efforts. Our results also emphasize the need to search for mutations in a comprehensive manner while still searching for both common and rare PTMs.
机译:今天,我们有前所未有的人体基因组和蛋白质组学数据,似乎正在快速接近我们目前对全面覆盖的理解。由于蛋白质组学搜索空间的巨大增加,将基因组信息与霰弹枪蛋白质组学组合仍然具有挑战性。然而,使基因组和蛋白质组学信息之间的这种联系对于癌症研究至关重要。此外,随着我​​们对个性化医学的进展,蛋白质组学分析至关重要,以确定个体突变和变体,以完全理解蛋白质网络并培养个性化疗法。虽然这些优势很好,但只有少数研究表明蛋白质组学数据与大型基因组输入的成功集成。我们展示并审视螺栓的能力,这是一种新的基于云的蛋白质组学搜索引擎,用于在几分钟内搜索超过230万已知的癌症突变,同时仍然表演包括31个翻译后修改的标准蛋白质组学搜索。我们使用先前公布的蛋白质组学数据集并识别使用基因组研究验证的突变以及以前的蛋白质组学的努力。我们的结果还强调需要以全面的方式搜索突变,同时仍在寻找常见和罕见的PTM。

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