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IGDB.NSCLC: integrated genomic database of non-small cell lung cancer

机译:IGDB.NSCLC:非小细胞肺癌的综合基因组数据库

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摘要

Lung cancer is the most common cause of cancer-related mortality with more than 1.4 million deaths per year worldwide. To search for significant somatic alterations in lung cancer, we analyzed, integrated and manually curated various data sets and literatures to present an integrated genomic database of non-small cell lung cancer (IGDB.NSCLC, http://igdb.nsclc.ibms.sinica.edu.tw). We collected data sets derived from hundreds of human NSCLC (lung adenocarcinomas and/or squamous cell carcinomas) to illustrate genomic alterations [chromosomal regions with copy number alterations (CNAs), gain/loss and loss of heterozygosity], aberrant expressed genes and microRNAs, somatic mutations and experimental evidence and clinical information of alterations retrieved from literatures. IGDB.NSCLC provides user friendly interfaces and searching functions to display multiple layers of evidence especially emphasizing on concordant alterations of CNAs with co-localized altered gene expression, aberrant microRNAs expression, somatic mutations or genes with associated clinicopathological features. These significant concordant alterations in NSCLC are graphically or tabularly presented to facilitate and prioritize as the putative cancer targets for pathological and mechanistic studies of lung tumorigenesis and for developing new strategies in clinical interventions.
机译:肺癌是与癌症相关的死亡的最常见原因,全球每年有140万以上的死亡。为了寻找肺癌的重大体细胞改变,我们分析,整合和手动整理了各种数据集和文献,以提供非小细胞肺癌的整合基因组数据库(IGDB.NSCLC,http://igdb.nsclc.ibms。 sinica.edu.tw)。我们收集了数百种人类NSCLC(肺腺癌和/或鳞状细胞癌)的数据集,以说明基因组变化[具有拷贝数变化(CNA)的染色体区域,杂合性的增/减和损失],异常表达的基因和microRNA,体细胞突变和实验证据以及从文献中检索到的改变的临床信息。 IGDB.NSCLC提供用户友好的界面和搜索功能,以显示多层证据,尤其强调与共同定位的改变的基因表达,异常的microRNA表达,体细胞突变或具有相关临床病理特征的基因一致的CNA改变。以图形或表格形式显示了NSCLC中这些显着一致的变化,以促进肺癌发生的病理学和机制研究以及在临床干预中制定新的策略,并以此作为推定的癌症靶标。

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