Publications by authors named "Olivier Tremblay Savard"

Article Synopsis
  • A study found that many patients with kidney failure experience increased hospital visits before starting dialysis, prompting the need for better remote health monitoring.
  • The VIEWER trial focused on using a telemonitoring system to keep track of patients' vitals and evaluate both adherence and acceptance in a population at high risk for advancing kidney disease.
  • While the first phase showed higher adherence rates (77.17%) compared to the second phase (36%), participants recognized benefits like better health awareness but also faced challenges such as connectivity issues and health-related anxieties.
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Classical compartmental models of infectious disease assume that spread occurs through a homogeneous population. This produces poor fits to real data, because individuals vary in their number of epidemiologically-relevant contacts, and hence in their ability to transmit disease. In particular, network theory suggests that super-spreading events tend to happen more often at the beginning of an epidemic, which is inconsistent with the homogeneity assumption.

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Background: Glomerulonephritis (GN) represents a common cause of chronic kidney disease, and treatment to slow or prevent progression of GN is associated with significant morbidity. Large patient registries have improved the understanding of risk stratification, treatment selection, and definitions of treatment response in GN, but can be resource-intensive, with incomplete patient capture.

Objective: To describe the creation of a comprehensive clinicopathologic registry for all patients undergoing kidney biopsy in Manitoba, using natural language processing software for data extraction from pathology reports, as well as to describe cohort characteristics and outcomes.

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Clustering is a central task in many data analysis applications. However, there is no universally accepted metric to decide the occurrence of clusters. Ultimately, we have to resort to a consensus between experts.

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In phylogenetic networks, picking a cherry consists of removing a leaf that shares a parent with another leaf, or removing a reticulate edge whose endpoints are parents of leaves. Cherry-picking operations were recently shown to have several structural and algorithmic applications in the study of networks, for instance in determining their reconstructibility or in solving the network hybridization and network containment problems. In particular, some networks within certain classes are isomorphic if they can be reduced to a single node by the same sequence of cherry-picking operations.

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We present BOPAL 2.0, an improved version of the BOPAL algorithm for the evolutionary history inference of tRNA and rRNA genes in bacterial genomes. Our approach can infer complete evolutionary scenarios and ancestral gene orders on a phylogeny and considers a wide range of events such as duplications, deletions, substitutions, inversions and transpositions.

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Background: In bacterial genomes, rRNA and tRNA genes are often organized into operons, i.e. segments of closely located genes that share a single promoter and are transcribed as a single unit.

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Background: Secondary structures form the scaffold of multiple sequence alignment of non-coding RNA (ncRNA) families. An accurate reconstruction of ancestral ncRNAs must use this structural signal. However, the inference of ancestors of a single ncRNA family with a single consensus structure may bias the results towards sequences with high affinity to this structure, which are far from the true ancestors.

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Article Synopsis
  • OrthoAlign is a new algorithm designed to tackle the gene order alignment problem, specifically for orthologs, by considering key evolutionary events like duplications and rearrangements.
  • When applied to the tRNA gene repertoires of 50 bacteria from the Bacillus genus, it revealed that gene duplications and losses are more common than rearrangements.
  • The study found that the rates of gene duplications and losses in Bacillus are significantly lower than in E. coli, indicating strong selective pressures on the tRNA genes in this genus.
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Understanding the history of a gene family that evolves through duplication, speciation, and loss is a fundamental problem in comparative genomics. Features such as function, position, and structural similarity between genes are intimately connected to this history; relationships between genes such as orthology (genes related through a speciation event) or paralogy (genes related through a duplication event) are usually correlated with these features. For example, recent work has shown that in human and mouse there is a strong connection between function and inparalogs, the paralogs that were created since the speciation event separating the human and mouse lineages.

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Background: Tandemly Arrayed Gene (TAG) clusters are groups of paralogous genes that are found adjacent on a chromosome. TAGs represent an important repertoire of genes in eukaryotes. In addition to tandem duplication events, TAG clusters are affected during their evolution by other mechanisms, such as inversion and deletion events, that affect the order and orientation of genes.

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Given a phylogenetic tree involving whole genome duplication events, we contribute to solving the problem of computing the rearrangement and double cut-and-join (DCJ) distances on a branch of the tree linking a duplication node d to a speciation node or a leaf s. In the case of a genome G at s containing exactly two copies of each gene, the genome halving problem is to find a perfectly duplicated genome D at d minimizing the rearrangement distance with G. We generalize the existing exact linear-time algorithm for genome halving to the case of a genome G with missing gene copies.

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