rbf-tss identification of transcription start site in human using radial basis functions network and oligonucleotide positional frequenciesrbf-tss转录开始网站的识别在人类使用径向基函数网络和寡核苷酸位置频率.pdfVIP
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rbf-tss identification of transcription start site in human using radial basis functions network and oligonucleotide positional frequenciesrbf-tss转录开始网站的识别在人类使用径向基函数网络和寡核苷酸位置频率
RBF-TSS: Identification of Transcription Start Site
in Human Using Radial Basis Functions Network
and Oligonucleotide Positional Frequencies
Rami N. Mahdi, Eric C. Rouchka*
Department of Computer Engineering and Computer Science, University of Louisville, Louisville, Kentucky, United States of America
Abstract
Accurate identification of promoter regions and transcription start sites (TSS) in genomic DNA allows for a more complete
understanding of the structure of genes and gene regulation within a given genome. Many recently published methods
have achieved high identification accuracy of TSS. However, models providing more accurate modeling of promoters and
TSS are needed. A novel identification method for identifying transcription start sites that improves the accuracy of TSS
recognition for recently published methods is proposed. This method incorporates a metric feature based on
oligonucleotide positional frequencies, taking into account the nature of promoters. A radial basis function neural
network for identifying transcription start sites (RBF-TSS) is proposed and employed as a classification algorithm. Using non-
overlapping chunks (windows) of size 50 and 500 on the human genome, the proposed method achieves an area under the
Receiver Operator Characteristic curve (auROC) of 94.75% and 95.08% respectively, providing increased performance over
existing TSS prediction methods.
Citation: Mahdi RN, Rouchka EC (2009) RBF-TSS: Identification of Transcription Start Site in Human Using Radial Basis Functions Network and Oligonucleotide
Positional Frequencies. PLoS ONE 4(3): e4878. doi:10.1371/journal.pone.0004878
Editor: Darren P. Martin, Institute of Infectious Disease and Molecular Medicine, South Africa
Received October 23, 2008; Accepted February 20, 2009; Published March 16, 2009
Copyright: 20
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