| Literature DB >> 33765283 |
Pieter Spealman1, Armaghan Naik2, Joel McManus3.
Abstract
The identification of upstream open reading frames (uORFs) using ribosome profiling data is complicated by several factors such as the noise inherent to the procedure, the substantial increase in potential translation initiation sites (and false positives) when one includes non-canonical start codons, and the paucity of molecularly validated uORFs. Here we present uORF-seqr, a novel machine learning algorithm that uses ribosome profiling data, in conjunction with RNA-seq data, as well as transcript aware genome annotation files to identify statistically significant AUG and near-cognate codon uORFs.Entities:
Keywords: Alternative translation initiation site; Near-cognate codon; Non-canonical start codon; Translational regulation; Upstream open reading frame; uORF
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Year: 2021 PMID: 33765283 DOI: 10.1007/978-1-0716-1150-0_15
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745