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- W2102496723 abstract "Ribosome profiling is a technique that permits genome-wide, quantitative analysis of translation and has found broad application in recent years. Here we describe a modified profiling protocol and software package designed to benefit more broadly the translation community in terms of simplicity and utility. The protocol, applicable to diverse organisms, including organelles, is based largely on previously published profiling methodologies, but uses duplex-specific nuclease (DSN) as a convenient, species-independent way to reduce rRNA contamination. We show that DSN-based depletion compares favorably with other commonly used rRNA depletion strategies and introduces little bias. The profiling protocol typically produces high levels of triplet periodicity, facilitating the detection of coding sequences, including upstream, downstream, and overlapping open reading frames (ORFs) and an alternative ribosome conformation evident during termination of protein synthesis. In addition, we provide a software package that presents a set of methods for parsing ribosomal profiling data from multiple samples, aligning reads to coding sequences, inferring alternative ORFs, and plotting average and transcript-specific aspects of the data. Methods are also provided for extracting the data in a form suitable for differential analysis of translation and translational efficiency." @default.
- W2102496723 created "2016-06-24" @default.
- W2102496723 creator A5003756828 @default.
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- W2102496723 creator A5046652547 @default.
- W2102496723 creator A5050195392 @default.
- W2102496723 creator A5056217079 @default.
- W2102496723 date "2015-08-18" @default.
- W2102496723 modified "2023-10-12" @default.
- W2102496723 title "The use of duplex-specific nuclease in ribosome profiling and a user-friendly software package for Ribo-seq data analysis" @default.
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- W2102496723 doi "https://doi.org/10.1261/rna.052548.115" @default.
- W2102496723 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4574750" @default.
- W2102496723 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26286745" @default.
- W2102496723 hasPublicationYear "2015" @default.