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Boucoiran, I.

Publications and source records attributed to Boucoiran, I..

3 recordsLinked to original sources

KmerSignificance Score: A discriminative and biologically-informed framework for viral k-mer prioritization

Distinguishing closely related viral strains requires identifying genomic regions where subtle sequence differences carry biological significance. While k-mer-based approaches offer computational efficiency for genome analysis, existing methods lack standardized frameworks for evaluating which k-mers are most informative. Current selection strategies focus primarily on statistical discriminative power without integrating biological relevance. We introduce KmerSignificance Score (KSS), a k-mer prioritization framework combining three components: an information-theoretic method measuring strain-distinguishing capacity, an optimized amino acid substitution matrix (MIYATA EVO) for mutation impact assessment, and protein-level functional importance scoring derived from UniProt annotations. KSS produces standardized scores in the [0, 1] interval, enabling direct cross-dataset comparison. The discriminative component achieved classification performance comparable or superior to all tested alternatives (mean F1 = 0.880 vs. 0.718-0.877 for six established methods) while additionally providing bounded scores with consistent empirical distributions for cross-dataset comparability. MIYATA EVO, optimized via genetic algorithm, improved biophysical property correlations by 28.4% over the original MIYATA matrix. Protein scoring on 17,470 viral proteins showed robust agreement with UniProt annotation scores (Kendall{tau} = 0.777) while revealing finer functional distinctions. Literature validation on SARS-CoV-2 (278,738 sequences, 19 variants), HIV-1 (12,223 sequences, 15 subtypes), and human cytomegalovirus (HCMV; 399-646 sequences, 4-8 genotypes) confirmed that high-scoring k-mers consistently map to established variant-defining mutations, subtype-specific polymorphisms, and genotype markers. KSS provides a standardized framework for viral k-mer prioritization with applications in variant surveillance, molecular epidemiology, and functional annotation. The tool is available at https://github.com/bioinfoUQAM/KmerSignificanceScore. Author summaryIdentifying genetic differences between closely related viral strains is essential for pandemic preparedness, vaccine development, and understanding disease outbreaks. With millions of viral genomes now sequenced, researchers need tools that can rapidly pinpoint which genomic differences matter most biologically, not just which are statistically distinctive. Current k-mer-based approaches identify patterns that distinguish viral strains but cannot assess whether those differences affect protein function or disease phenotype. We developed KmerSignificance Score (KSS), a framework that we designed to rank short genomic sequences by combining three types of evidence: how well they distinguish viral strains, how much the encoded amino acid changes affect protein properties, and how functionally important the affected protein is. We standardized the resulting scores on a 0-to-1 scale, allowing direct comparison across different viruses and studies. We validated our framework on three major human pathogens (SARS-CoV-2, HIV-1, and human cytomegalovirus) and found that top-scoring positions consistently correspond to sites with documented roles in immune evasion, drug resistance, viral fitness, and strain classification. Our framework can help prioritize genomic features for surveillance of emerging variants, guide experimental validation, and support molecular epidemiology.

bioinformatics↗

Machine learning-based approach KEVOLVE efficiently identifies SARS-CoV-2 variant-specific genomic signatures

Machine learning was shown to be effective at identifying distinctive genomic signatures among viral sequences. These signatures are defined as pervasive motifs in the viral genome that allow discrimination between species or variants. In the context of SARS-CoV-2, the identification of these signatures can assist in taxonomic and phylogenetic studies, improve in the recognition and definition of emerging variants, and aid in the characterization of functional properties of polymorphic gene products. In this paper, we assess KEVOLVE, an approach based on a genetic algorithm with a machine-learning kernel, to identify multiple genomic signatures based on minimal sets of k-mers. In a comparative study, in which we analyzed large SARS-CoV-2 genome dataset, KEVOLVE was more effective at identifying variant-discriminative signatures than several gold-standard statistical tools. Subsequently, these signatures were characterized using a new extension of KEVOLVE (KANALYZER) to highlight variations of the discriminative signatures among different classes of variants, their genomic location, and the mutations involved. The majority of identified signatures were associated with known mutations among the different variants, in terms of functional and pathological impact based on available literature. Here we showed that KEVOLVE is a robust machine learning approach to identify discriminative signatures among SARS-CoV-2 variants, which are frequently also biologically relevant, while bypassing multiple sequence alignments. The source code of the method and additional resources are available at: https://github.com/bioinfoUQAM/KEVOLVE.

bioinformatics↗

Robust Tobacco Smoking Self-Report in two Cohorts of Vulnerable Pregnant Women and Adults

BackgroundStigma associated with tobacco smoking, especially during pregnancy, may lead to underreporting and possible bias in studies relying on self-reported smoking data. Cotinine, a nicotine metabolite with a [~]20h half-life in blood, is often used as a biomarker of smoking. The objective of this study was to examine the concordance between self-reported smoking and plasma cotinine concentration among participants enrolled in two related cohorts of vulnerable individuals: human immunodeficiency virus (HIV)-positive and HIV-negative pregnant women enrolled in the CARMA-PREG cohort and HIV-positive and HIV-negative non-pregnant women and men enrolled in the CARMA-CORE cohort. MethodsFor HIV-positive (n=76) and negative (n=24) pregnant women, plasma cotinine was measured by ELISA in specimens collected during the third trimester, between 28 and 38 weeks of gestation. Plasma cotinine was also measured in HIV-positive (n=43) and negative (n=57) women and men enrolled in the CARMA-CORE cohort. ResultsSelf-reported smokers were more likely to have low income (p<0.001) in both cohorts, and to deliver preterm (p=0.007) in CARMA-PREG. In the CARMA-PREG cohort, concordance between plasma cotinine was 95% for self-reported smoking, and 89% for self-reported non-smoking. In the CARMA-CORE cohort we observed similarly high concordances of 96% and 92% for self-reported smoking and non-smoking, respectively. In this sample, the odds of discordance between self-reported smoking status and cotinine levels were not significantly different between self-reported smokers and non-smokers, nor between pregnant women and others. Taken together, the overall concordance between plasma cotinine and self-reported data was 94% with a Cohens kappa coefficient of 0.860 among all participants. ConclusionsGiven the high proportion of vulnerable people in the CARMA-PREG and CARMA-CORE cohorts, our results may not be fully generalizable to the general population. However, they demonstrate that participant surveying in a non-judgemental context can lead to accurate and robust self-report data. ImplicationsReliable self-reported smoking data is necessary to account for smoking status in subsequent studies. Our results suggest that future studies should ensure that study participants feel sale to speak candidly to non-judgemental research staff to obtain reliable self-report data.

pathology↗