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FANTOM5 CAGE profiles of human and mouse samples

机译:人类和小鼠样品的FANTOM5 CAGE配置文件

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摘要

In the FANTOM5 project, transcription initiation events across the human and mouse genomes were mapped at a single base-pair resolution and their frequencies were monitored by CAGE (Cap Analysis of Gene Expression) coupled with single-molecule sequencing. Approximately three thousands of samples, consisting of a variety of primary cells, tissues, cell lines, and time series samples during cell activation and development, were subjected to a uniform pipeline of CAGE data production. The analysis pipeline started by measuring RNA extracts to assess their quality, and continued to CAGE library production by using a robotic or a manual workflow, single molecule sequencing, and computational processing to generate frequencies of transcription initiation. Resulting data represents the consequence of transcriptional regulation in each analyzed state of mammalian cells. Non-overlapping peaks over the CAGE profiles, approximately 200,000 and 150,000 peaks for the human and mouse genomes, were identified and annotated to provide precise location of known promoters as well as novel ones, and to quantify their activities.
机译:在FANTOM5项目中,跨人类和小鼠基因组的转录起始事件以单个碱基对的分辨率进行定位,并通过CAGE(基因表达的上限分析)与单分子测序相结合来监测其频率。在细胞活化和发育过程中,大约三千个样本(包括各种原代细胞,组织,细胞系和时间序列样本)经历了统一的CAGE数据生成流程。分析流程首先测量RNA提取物以评估其质量,然后继续通过使用机器人或手动工作流程,单分子测序和计算处理来生成转录起始频率来进行CAGE文库生产。结果数据代表在每种分析的哺乳动物细胞状态下转录调控的结果。识别并注释了CAGE谱上的非重叠峰,即人类和小鼠基因组的大约200,000和150,000峰,以提供已知启动子和新启动子的精确位置,并对其活性进行定量。

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