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Casiraghi, E.

Publications and source records attributed to Casiraghi, E..

3 recordsLinked to original sources

Node-degree aware edge sampling mitigates inflated classification performance in biomedical graph representation learning

Graph representation learning is a family of related approaches that learn low-dimensional vector representations of nodes and other graph elements called embeddings. Embeddings approximate characteristics of the graph and can be used for a variety of machine-learning tasks such as novel edge prediction. For many biomedical applications, partial knowledge exists about positive edges that represent relationships between pairs of entities, but little to no knowledge is available about negative edges that represent the explicit lack of a relationship between two nodes. For this reason, classification procedures are forced to assume that the vast majority of unlabeled edges are negative. Existing approaches to sampling negative edges for training and evaluating classifiers do so by uniformly sampling pairs of nodes. We show here that this sampling strategy typically leads to sets of positive and negative edges with imbalanced edge degree distributions. Using representative homogeneous and heterogeneous biomedical knowledge graphs, we show that this strategy artificially inflates measured classification performance. We present a degree-aware node sampling approach for sampling negative edge examples that mitigates this effect and is simple to implement.

bioinformatics↗

An algorithmic framework for isoform-specific functional analysis

Gene Ontology (GO) overrepresentation analysis characterizes the biological mechanisms common to sets of differentially expressed genes identified by high-throughput experiments. To date, GO overrepresentation analysis has mainly been used to evaluate differentially expressed genes, but short- and long-read RNA-seq technologies now allow increasingly accurate identification of differential alternative splicing. The function of most splice isoforms remain unknown, but if acccurate predictions could be made, overrepresentation analysis could be applied to differentially spliced isoforms to assess the functional implications of alternative splicing in RNA-seq experiments. We present isopret (Isoform Interpretation), a new paradigm for isoform function prediction based on the expectation-maximization framework. isopret leverages the relationships between sequence and functional isoform similarity to infer isoform specific functions in a highly accurate fashion. This enabled us to adapt GO overrepresentation analysis, which to date has been limited to differential gene expression, to be extended to assess overrepresentation of GO annotations in differentially spliced isoforms. An analysis of 100 RNA-seq studies including investigations of development, cancer, and common disease demonstrated that expression and splicing regulate different sets of biological functions. We make isopret predictions freely available in a desktop application that can be used to analyze differential expression and splicing in any bulk RNA-seq dataset.

bioinformatics↗

Supervised learning with word embeddings derived from PubMed captures latent knowledge about protein kinases and cancer

Inhibiting protein kinases (PKs) that cause cancers has been an important topic in cancer therapy for years. So far, almost 8% of more than 530 PKs have been targeted by FDA-approved medications and around 150 protein kinase inhibitors (PKIs) have been tested in clinical trials. We present an approach based on natural language processing and machine learning to the relations between PKs and cancers, predicting PKs whose inhibition would be efficacious to treat a certain cancer. Our approach represents PKs and cancers as semantically meaningful 100-dimensional vectors based on co-occurrence patterns in PubMed abstracts. We use information about phase I-IV trials in ClinicalTrials.gov to construct a training set for random forest classification. In historical data, associations between PKs and specific cancers could be predicted years in advance with good accuracy. Our model may be a tool to predict the relevance of inhibiting PKs with specific cancers.

bioinformatics↗