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Updated: Jul 6, 2025

De novo Identification of Actively Translated Open Reading Frames with Ribosome Profiling Data
Published on: February 18, 2022
GTax: improving de novo transcriptome assembly by removing foreign RNA contamination
Roberto Vera Alvarez1, David Landsman2
1Computational Biology Branch, National Center for Biotechnology Information, Intramural Research Program, National Library of Medicine, NIH, Bethesda, MD, USA.
Abstract:
The cost and complexity of generating a complete reference genome means that many organisms lack an annotated reference. An alternative is to use a de novo reference transcriptome. This technology is cost-effective but is susceptible to off-target RNA contamination. In this manuscript, we present GTax, a taxonomy-structured database of genomic sequences that can be used with BLAST to detect and remove foreign contamination in RNA sequencing samples before assembly. In addition, we use a de novo transcriptome assembly of Solanum lycopersicum (tomato) to demonstrate that removing foreign contamination in sequencing samples reduces the number of assembled chimeric transcripts.
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