@article { ISI:000371693900021,
	title = {No promoter left behind (NPLB): learn de novo promoter architectures from genome-wide transcription start sites},
	journal = {Bioinformatics},
	volume = {32},
	number = {5},
	year = {2016},
	month = {MAR},
	pages = {779-781},
	publisher = {OXFORD UNIV PRESS},
	address = {GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND},
	abstract = {<p>Promoters have diverse regulatory architectures and thus activate genes differently. For example, some have a TATA-box, many others do not. Even the ones with it can differ in its position relative to the transcription start site (TSS). No Promoter Left Behind (NPLB) is an efficient, organism-independent method for characterizing such diverse architectures directly from experimentally identified genome-wide TSSs, without relying on known promoter elements. As a test case, we show its application in identifying novel architectures in the fly genome.</p>},
	issn = {1367-4803},
	doi = {10.1093/bioinformatics/btv645},
	author = {Mitra, Sneha and Narlikar, Leelavati}
}
