Paul D. Donovan

dblp:309/3634 · DBLP profile ↗
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1ranked-venue papers
1as first author
1since 2021 · last 2021
0000-0002-3927-8961ORCID · reported

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author · 1 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › gene expression analysis
differential expression analysis
0.512021
tsRNAsearch: a pipeline for the identification of tRNA and ncRNA fragments from small RNA-sequencing data · Bioinform. 2021
Bioinformatics and computational biology › transcriptomics
non-coding RNA analysis
0.512021
tsRNAsearch: a pipeline for the identification of tRNA and ncRNA fragments from small RNA-sequencing data · Bioinform. 2021
Bioinformatics and computational biology › transcriptomics
RNA-seq analysis
0.512021
tsRNAsearch: a pipeline for the identification of tRNA and ncRNA fragments from small RNA-sequencing data · Bioinform. 2021
Bioinformatics and computational biology
biomarker discovery
0.112021
tsRNAsearch: a pipeline for the identification of tRNA and ncRNA fragments from small RNA-sequencing data · Bioinform. 2021

Methods — techniques the papers use, named apart from their topics

nextflow pipeline · 0.5
YearPublicationVenuePosition
2021 tsRNAsearch: a pipeline for the identification of tRNA and ncRNA fragments from small RNA-sequencing data
abstract
MOTIVATION: tRNAs were originally considered uni-functional RNA molecules involved in the delivery of amino acids to growing peptide chains on the ribosome. More recently, the liberation of tRNA fragments from tRNAs via specific enzyme cleavage has been characterized. Detection of tRNA fragments in sequencing data is difficult due to tRNA sequence redundancy and the short length of both tRNAs and their fragments. RESULTS: Here, we introduce tsRNAsearch, a Nextflow pipeline for the identification of differentially abundant tRNA fragments and other non-coding RNAs from small RNA-sequencing data. tsRNAsearch is intended for use when comparing two groups of datasets, such as control and treatment groups. tsRNAsearch comparatively searches for tRNAs and ncRNAs with irregular read distribution profiles (a proxy for RNA cleavage) using a combined score made up of four novel methods and a differential expression analysis, and reports the top ranked results in simple PDF and TEXT files. In this study, we used publicly available small RNA-seq data to replicate the identification of tsRNAs from chronic hepatitis-infected liver tissue data. In addition, we applied tsRNAsearch to pancreatic ductal adenocarcinoma (PDAC) and matched healthy pancreatic tissue small RNA-sequencing data. Our results support the identification of miR135b from the original study as a potential biomarker of PDAC and identify other potentially stronger miRNA biomarkers of PDAC. AVAILABILITY AND IMPLEMENTATION: https://github.com/GiantSpaceRobot/tsRNAsearch. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Paul D. Donovan, Natalie M. McHale, Morten T. Venø, Jochen H. M. Prehn
Bioinform.1