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Biology subjects

Selby, K.

Publications and source records attributed to Selby, K..

3 recordsLinked to original sources

Bayesian model-based method for clustering gene expression time series with multiple replicates

In this study, we introduce a Bayesian model-based method for clustering transcriptomics time series data with multiple replicates. This technique is based on sampling Gaussian processes (GPs) within an infinite mixture model from a Dirichlet process (DP). Our method uses multiple GP models to accommodate for multiple differently behaving experimental replicates within each cluster. We call it multiple models Dirichlet process Gaussian process (MMDPGP). We compare our method with state-of-the-art model-based clustering approaches for handling gene expression time series with multiple replicates. We present a case study where all methods are applied for clustering RNA-Seq time series of Clostridium botulinum with three different experimental replicates. The results obtained from the gene enrichment analysis showed that the number of significantly enriched sets of genes is larger in the clusters produced by MMDPGP. To demonstrate the accuracy of our method we use it to cluster synthetically generated data sets. The clusters produced by our method on the synthetic data had a significantly higher purity score compared to the state-of-the-art approaches. By modelling each replicate with a separate GP, our method can use the natural variability between experimental replicates to learn more about the underlying biology. Author summaryIn our manuscript we introduce a method called multiple models Dirichlet process Gaussian process (MMDPGP), a novel Bayesian approach for clustering gene expression time series data. Our method stands out by accounting for the variability among multiple experimental replicates within each cluster, a feature that is often overlooked in existing model-based clustering approaches. This allows us to capture the natural variability between replicates as opposed to the crude method of simply averaging the replicates which discards interesting information in the data. By integrating multiple Gaussian process models within an infinite mixture model derived from a Dirichlet process, MMDPGP offers a more nuanced and accurate representation of the biological data. We benchmarked MMDPGP against state-of-the-art methods, by applying them for the purpose of clustering recently collected RNA-Seq time series of the bacterium Clostridium botulinum and performing a gene enrichment analysis on the generated clusters. Additionally, we test the accuracy of our method in comparison with other methods using synthetic data sets. The superior performance of our method in terms of finding significantly enriched gene sets and the clustering accuracy on synthetic data underscore its robustness and potential for broad applicability in computational biology. Our study addresses a critical gap in the analysis of transcriptomics time series data by explicitly modeling the natural variability across experimental replicates. This advancement not only enhances the accuracy of clustering results but also provides deeper insights into the underlying biological processes. By leveraging Bayesian methods and Gaussian processes, our approach offers a powerful tool that can be adapted and extended for various types of omics data, inspiring further methodological developments in the field. Competing interestsWe declare no competing interests related to this work. Code availability and implementationThe Python code for implementing our method is publicly available in Zenodo through the following DOI link: https://doi.org/10.5281/zenodo.11202145. DataThe RNA-Seq data used to validate our method in the paper are deposited in GEO at the following link: https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE248529.

bioinformatics↗

Temperate grass allergy season defined by spatio-temporal shifts in airborne pollen communities

Grass pollen is the worlds most harmful outdoor aeroallergen and sensitivity varies between species. Different species of grass flower at different times, but it is not known how airborne communities of grass pollen change in time and space. Persistence and high mobility of grass pollen could result in increasingly diverse seasonal pollen communities. Conversely, if grass pollen does not persist for an extended time in the air, shifting pollen communities would be predicted throughout the summer months. Here, using targeted high throughput sequencing, we tracked the seasonal progression of airborne Poaceae pollen biodiversity across Britain, throughout the grass allergy season. All grass genera displayed discrete, temporally restricted peaks of pollen incidence which varied with latitude, revealing that the taxonomic composition of grass pollen exposure changes substantially across the allergy season. By developing more refined aeroallergen profiling, we predict that our findings will facilitate the exploration of links between taxon-specific exposure of harmful grass pollen and disease, with concomitant socio-economic benefits.

ecology↗

Diagnostic Yield And Treatment Impact Of Targeted Exome Sequencing In Early-Onset Epilepsy

BackgroundTo examine the impact on diagnosis, treatment and cost with early use of targeted whole-exome sequencing (WES) in early-onset epilepsy.\n\nMethodsWES was performed on 50 patients with early-onset epilepsy ([&le;] 5 years) of unknown cause. Patients were classified as retrospective (epilepsy diagnosis > 6 months) or prospective (epilepsy diagnosis < 6 months). WES was performed on an Ion ProtonTM and variant reporting was restricted to the sequences of 565 known epilepsy genes. Diagnostic yield and time to diagnosis were calculated. An analysis of cost and impact on treatment was also performed.\n\nResultsA likely/definite diagnosis was made in 17/50 patients (34%) with immediate treatment implications in 8/17 (47%). A possible diagnosis was identified in 9 additional patients (18%) for whom supporting evidence is pending. Time from epilepsy onset to genetic diagnosis was faster when WES was performed early in the diagnostic process (mean: 143 days prospective versus 2,172 days retrospective). Costs of prior negative tests averaged $8,344 in the retrospective group, suggesting savings of up to $5,110 per patient.\n\nInterpretationThese results support the clinical utility and potential cost-effectiveness of using targeted WES early in the diagnostic workup of patients with unexplained early-onset epilepsy. The costs and clinical benefits are likely to continue to improve. Advances in precision medicine and further studies regarding impact on long-term clinical outcome will be important.

genetics↗