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Thomas, E.

Publications and source records attributed to Thomas, E..

2 recordsLinked to original sources

A Bayesian inference tool for identifying artifactual calls from differential transcript abundance analyses

Relative transcript abundance has proven to be a valuable tool for inferring the phenotype of biological systems from genetic material. Several methods for the analysis of differential transcript abundance have been developed, and some of the most popular are based on negative binomial models. Although most genes are fitted reasonably well by the negative binomial distribution, the presence of outlier observations that do not fit such models can lead to artifactual identification of significant changes in transcription. Identifying those transcripts for the correct interpretation of results is extremely important. A robust and automated tool for detecting sample/transcript pairs that do not fit a negative binomial regression model is currently lacking. Here we propose ppcseq, a robust statistical framework that models hierarchically sample- and gene-wise features such as sequencing depth bias, the association between mean transcript abundance and its over-dispersion, and provides a theoretical transcript abundance distribution, on which the observed transcript abundance can be tested for outliers. We show using a publicly available data set where nearly 10% of differentially abundant transcripts had fold change inflated by the presence of outliers. This method has broad utility in filtering artifactual results of differential transcript abundance analyses based on a negative binomial framework.

bioinformatics

A novel real-time PCR assay panel for detection of common respiratory pathogens in a convenient, strip-tube array format

Commercial multiplex assays, built on different chemistries and platforms are widely available for simultaneous detection of pathogens that cause respiratory infections. However, these tests are often difficult to implement in a resource limited setting because of high cost. In this study, we developed and validated a method for simultaneous testing of common respiratory pathogens (Respanel) by real-time PCR in a convenient, strip-tube array format. Primers and probes for sixteen PCR assays were selected from the literature or newly designed. Following optimization of individual PCR assays, strip-tube arrays were prepared by dispensing primer-probe mixes (PPM) into two sets of 8-tube strips. Nucleic acid extracts from specimens were mixed with PCR master mix, and dispensed column-wise into 2X8-wells of a 96-well plate. PPMs from strip-tubes were then added to the wells using a multichannel pipette for real-time PCR. Individual PCR assays were optimized using previously known specimens (n=397) with 91%-100% concordance with culture, DFA or PCR results. Respanel was then tested in a routine manner at two different sites using specimens (n=147) previously tested by Qiagen Resplex I&II or Fast-Track Diagnostics Respiratory Pathogens 21 assays. The sensitivity, specificity and accuracy of Respanel were 94%, 95% and 95%, respectively, against Resplex and 88%, 100% and 99%, respectively, against FTDRP21. Respanel detected 48% more pathogens (p<0.05) than Resplex but the rate of pathogen detection was not significantly different from FTDRP21. Respanel is a convenient and inexpensive assay that is more sensitive than Resplex and comparable to FTDRP21 for the detection of common respiratory pathogens.

pathology