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Identification and utilization of copy number information for correcting Hi-C contact map of cancer cell lines

机译:校正和利用校正癌细胞系Hi-C联系地图的拷贝数信息

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摘要

HiCNAtra pipeline and RD signal computation. a Block diagram of the HiCNAtra software showing different computational modules. b Schematic illustration of the RD signal computation methods using Hi-C (left) and 3C-seq (right) reads. Left: For Hi-C data, informative and non-informative (only dangling-end reads are shown) reads (top panel) mapped within the restriction fragment-end windows (second panel) are used for RD calculation. Then, the number of reads is counted for each window (third panel). Base counts are then estimated for each restriction fragment as the summation of the counts of its two fragment-end windows (bottom panel). Right: For 3C-seq data (top panel), genomic reads (middle panel) are exclusively used to compute the RD signal in an unbiased manner similar to WGS paired-end reads (bottom panel)
机译:HICNATRA管道和RD信号计算。显示不同计算模块的HICnatra软件的框图。 b使用Hi-C(左)和3C-SEQ(右)读取的RD信号计算方法的示意图。左:对于Hi-C数据,信息和非信息(仅显示悬挂端读取)映射在限制片段端窗口(第二面板)中的读取(顶面板)用于RD计算。然后,针对每个窗口(第三面板)计算读取的数量。然后针对每个限制片段估计基数作为其两个片段窗口窗口(底部面板)的数量的求和。右:对于3C-SEQ数据(顶部面板),基因组读取(中间板)专门用于以与WGS配对端读取的无偏见方式计算RD信号(底部面板)

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