Probabilistic identification of bacterial essential genes via insertion density using TraDIS data with Tn5 libraries

Motivation: Probabilistic Identification of bacterial essential genes using transposon-directed insertion-site sequencing (TraDIS) data based on Tn5 libraries has received relatively little attention in the literature; most methods are designed for mariner transposon insertions. Analysis of Tn5 tran...

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Bibliographic Details
Main Authors: Chaudhuri, R.R (Author), Nlebedim, V.U (Author), Walters, K. (Author)
Format: Article
Language:English
Published: Oxford University Press 2021
Online Access:View Fulltext in Publisher
LEADER 02445nam a2200157Ia 4500
001 10.1093-bioinformatics-btab508
008 220427s2021 CNT 000 0 und d
020 |a 13674803 (ISSN) 
245 1 0 |a Probabilistic identification of bacterial essential genes via insertion density using TraDIS data with Tn5 libraries 
260 0 |b Oxford University Press  |c 2021 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1093/bioinformatics/btab508 
520 3 |a Motivation: Probabilistic Identification of bacterial essential genes using transposon-directed insertion-site sequencing (TraDIS) data based on Tn5 libraries has received relatively little attention in the literature; most methods are designed for mariner transposon insertions. Analysis of Tn5 transposon-based genomic data is challenging due to the high insertion density and genomic resolution. We present a novel probabilistic Bayesian approach for classifying bacterial essential genes using transposon insertion density derived from transposon insertion sequencing data. We implement a Markov chain Monte Carlo sampling procedure to estimate the posterior probability that any given gene is essential. We implement a Bayesian decision theory approach to selecting essential genes. We assess the effectiveness of our approach via analysis of both simulated data and three previously published Escherichia coli, Salmonella Typhimurium and Staphylococcus aureus datasets. These three bacteria have relatively well characterized essential genes which allows us to test our classification procedure using receiver operating characteristic curves and area under the curves. We compare the classification performance with that of Bio-Tradis, a standard tool for bacterial gene classification. Results: Our method is able to classify genes in the three datasets with areas under the curves between 0.967 and 0.983. Our simulated synthetic datasets show that both the number of insertions and the extent to which insertions are tolerated in the distal regions of essential genes are both important in determining classification accuracy. Importantly our method gives the user the option of classifying essential genes based on the user-supplied costs of false discovery and false non-discovery. © 2021 The Author(s) 2021. Published by Oxford University Press. 
700 1 |a Chaudhuri, R.R.  |e author 
700 1 |a Nlebedim, V.U.  |e author 
700 1 |a Walters, K.  |e author 
773 |t Bioinformatics