RFECS: A Random-Forest Based Algorithm for Enhancer Identification from Chromatin State
Author(s) -
Nisha Rajagopal,
Wei Xie,
Yan Li,
Uli Wagner,
Wei Wang,
J Stamatoyannopoulos,
Jason Ernst,
Manolis Kellis,
Bing Ren
Publication year - 2013
Publication title -
plos computational biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.628
H-Index - 182
eISSN - 1553-7358
pISSN - 1553-734X
DOI - 10.1371/journal.pcbi.1002968
Subject(s) - enhancer , chromatin , computational biology , histone , biology , enhancer rnas , chia pet , epigenomics , genome , identification (biology) , random forest , regulation of gene expression , histone code , genetics , gene , chromatin remodeling , gene expression , computer science , nucleosome , artificial intelligence , dna methylation , botany
Transcriptional enhancers play critical roles in regulation of gene expression, but their identification in the eukaryotic genome has been challenging. Recently, it was shown that enhancers in the mammalian genome are associated with characteristic histone modification patterns, which have been increasingly exploited for enhancer identification. However, only a limited number of cell types or chromatin marks have previously been investigated for this purpose, leaving the question unanswered whether there exists an optimal set of histone modifications for enhancer prediction in different cell types. Here, we address this issue by exploring genome-wide profiles of 24 histone modifications in two distinct human cell types, embryonic stem cells and lung fibroblasts. We developed a Random-Forest based algorithm, RFECS ( R andom F orest based E nhancer identification from C hromatin S tates) to integrate histone modification profiles for identification of enhancers, and used it to identify enhancers in a number of cell-types. We show that RFECS not only leads to more accurate and precise prediction of enhancers than previous methods, but also helps identify the most informative and robust set of three chromatin marks for enhancer prediction.
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