Abstract
Three-dimensional (3D) conformation of the chromatin is crucial to stringently regulate gene expression patterns and DNA replication in a cell-type specific manner. Hi-C is a key technique for measuring 3D chromatin interactions genome wide. Estimating and predicting the resolution of a library is an essential step in any Hi-C experimental design. Here, we present the mathematical concepts to estimate the resolution of a dataset and predict whether deeper sequencing would enhance the resolution. We have developed HiCRes, a docker pipeline, by applying these concepts to several Hi-C libraries.
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CITATION STYLE
Marchal, C., Singh, N., Corso-Díaz, X., & Swaroop, A. (2022). HiCRes: a computational method to estimate and predict the genomic resolution of Hi-C libraries. Nucleic Acids Research, 50(6), E35. https://doi.org/10.1093/nar/gkab1235
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