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胶质瘤恶性进展中的全面 RNA-seq 转录组特征分析。

Comprehensive RNA-seq transcriptomic profiling in the malignant progression of gliomas.

机构信息

Beijing Neurosurgical Institute, Beijing 100050, China.

School of Medicine, Tsinghua University, Beijing 100084, China.

出版信息

Sci Data. 2017 Mar 14;4:170024. doi: 10.1038/sdata.2017.24.

Abstract

Gliomas are the most common and lethal intracranial tumours. RNA sequencing technologies and advanced data analyses recently enabled the characterization of transcriptomic information, including protein-coding gene expression, non-coding gene expression, alternative splicing, and fusion gene detection, to facilitate detection of diseases and altered phenotypes. As a part of the Chinese Glioma Genome Atlas (CGGA) project, our aim was to delineate comprehensive transcriptome profiling in the malignant progression of human gliomas. Three hundred twenty five gliomas with different grades were collected over the past twelve years. Using the Illumina HiSeq 2,000 system, over 92 million high quality 101-bp paired-end reads were generated per sample, yielding a total of 30 billion reads. This comprehensive dataset will be useful to deepen the comprehensive understanding of gliomas, providing an opportunity to generate new therapies, diagnoses, and preventive strategies.

摘要

神经胶质瘤是最常见和最致命的颅内肿瘤。RNA 测序技术和先进的数据分析方法最近使得对转录组信息的特征描述成为可能,包括蛋白质编码基因表达、非编码基因表达、可变剪接和融合基因检测,从而有助于疾病和表型改变的检测。作为中国神经胶质瘤基因组图谱 (CGGA) 项目的一部分,我们的目标是描绘人类神经胶质瘤恶性进展过程中的全面转录组谱。在过去的十二年中,我们收集了 325 例不同分级的神经胶质瘤。使用 Illumina HiSeq 2000 系统,每个样本生成超过 9200 万个高质量的 101bp 配对末端读数,总共产生了 300 亿个读数。这个全面的数据集将有助于加深对神经胶质瘤的全面了解,为开发新的治疗方法、诊断方法和预防策略提供机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2643/5349247/abfb47415030/sdata201724-f1.jpg

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