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FisHiCal: an R package for iterative FISH-based calibration of Hi-C data

机译:FisHiCal:R包,用于基于FISH的Hi-C数据的迭代校准

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摘要

The fluorescence in situ hybridization (FISH) method has been providing valuable information on physical distances between loci (via image analysis) for several decades. Recently, high-throughput data on nearby chemical contacts between and within chromosomes became available with the Hi-C method. Here, we present FisHiCal, an R package for an iterative FISH-based Hi-C calibration that exploits in full the information coming from these methods. We describe here our calibration model and present 3D inference methods that we have developed for increasing its usability, namely, 3D reconstruction through local stress minimization and detection of spatial inconsistencies. We next confirm our calibration across three human cell lines and explain how the output of our methods could inform our model, defining an iterative calibration pipeline, with applications for quality assessment and meta-analysis
机译:荧光原位杂交(FISH)方法几十年来一直提供有关基因座之间物理距离的有价值的信息(通过图像分析)。最近,通过Hi-C方法可以获得有关染色体之间和内部的附近化学接触的高通量数据。在这里,我们介绍FisHiCal,这是一个用于基于FISH的迭代Hi-C校准的R软件包,该软件包完全利用了来自这些方法的信息。我们在这里描述我们的校准模型,并介绍为提高其可用性而开发的3D推理方法,即通过局部应力最小化和空间不一致性检测进行3D重构。接下来,我们将确认在三种人类细胞系中的校准,并说明方法的输出如何为我们的模型提供信息,定义迭代校准管道,以及用于质量评估和荟萃分析的应用程序

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