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Pendleton, S. C.

Publications and source records attributed to Pendleton, S. C..

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Klarigi: Explanations for Semantic Groupings

BackgroundAnnotation of biomedical entities with ontology classes provides for formal semantic analysis and mobilisation of background knowledge in determining their relationships. To date enrichment analysis has been routinely employed to identify classes that are over-represented in annotations across sets of groups, such as biosample gene expression profiles or patient phenotypes. These approaches, however, usually consider only univariate relationships, make limited use of the semantic features of ontologies, and provide limited information and evaluation of the explanatory power of both singular and grouped candidate classes. Moreover, they do not solve the problem of deriving cohesive, characteristic, and discriminatory sets of classes for entity groups. ResultsWe have developed a new method, Klarigi, which introduces multiple scoring heuristics for identification of classes that are both compositional and discriminatory for groups of entities annotated with ontology classes. The tool includes a novel algorithm for derivation of multivariable semantic explanations for entity groups, makes use of semantic inference through live use of an ontology reasoner, and includes a classification method for identifying the discriminatory power of candidate sets. We describe the design and implementation of Klarigi, and evaluate its use in two test cases, comparing and contrasting methods and results with literature and enrichment analysis methods. ConclusionsWe demonstrate that Klarigi produces characteristic and discriminatory explanations for groups of biomedical entities in two settings. We also show that these explanations recapitulate and extend the knowledge held in existing biomedical databases and literature for several diseases. We conclude that Klarigi provides a distinct and valuable perspective on biomedical datasets when compared with traditional enrichment methods, and therefore constitutes a new method by which biomedical datasets can be explored, contributing to improved insight into semantic data.

bioinformatics↗

An analysis of current state of the art software on nanopore metagenomic data

ContextOur insight into DNA is controlled through a process called sequencing. Until recently, it was only possible to sequence DNA into short strings called \"reads\". Nanopore is a new sequencing technology to produce significantly longer reads. Using nanopore sequencing, a single molecule of DNA can be sequenced without the need for time consuming PCR amplification (polymerase chain reaction is a technique used in molecular biology to amplify a single copy or a few copies of a segment of DNA across several orders of magnitude).\n\nAimsMetagenomics is the study of genetic material recovered from environmental samples. A research team from IBERS (Institute of Biological, Environmental & Rural Sciences) at Aberystwyth University have sampled metagenomes from a coal mine in South Wales using the Nanopore MinION and given initial taxonomic (classification of organisms) summaries of the contents of the microbial community.\n\nMethodsUsing various new software aimed for metagenomic data, we are interested to discover how well current bioinformatics software works with the data-set. We will conduct analysis and research into how well these new state of the art software works with this new long read data and try out some recent new developments for such analysis.\n\nResultsMost of the software we used worked very well: we gained understanding of the ACGT count and quality of the data. However some software for bioinformatics dont seem to work with nanopore data. Furthermore, we can conclude that low quality nanopore data may actually be quite average.

bioinformatics↗