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Becchi, T.

Publications and source records attributed to Becchi, T..

2 recordsLinked to original sources

KDM: embedding DNA/RNA motifs and sequences in a shared k-mer space for unified discovery, analysis and binding prediction

Motif discovery and binding-site prediction in DNA and RNA sequences are central tasks in regulatory genomics, yet the methodological landscape is split between interpretable but rigid position weight matrices (PWMs) and high-performing but opaque machine-learning models. We present KDM, a unifying framework in which both motifs and sequences are represented as probability distributions over a shared k-mer dictionary, embedded via the Hellinger transformation. This common geometry enables motif-sequence scoring, motif-motif comparison, de novo discovery, and binding prediction with a single primitive, the Bhattacharyya coefficient. We instantiate four tools on this representation: KDMMap for positional enrichment analysis, KDMMatch for information-content-aware motif matching, KDMFind for unsupervised motif discovery via projective non-negative matrix factorization, and KDM-LRLM for binding prediction with Lasso-regularized logistic regression. Across 1,324 transcription-factor ChIP-seq and 161 RBP eCLIP experiments, KDMMap matches CentriMos motif rankings in 84% of TF and 79% of RBP experiments, and KDMMatch agrees with Tomtom on motif annotation in 74.5% of TFs. On binding prediction across four datasets covering 2,475 experiments, KDM-LRLM matches or exceeds eight deep-learning and three k-mer-based competitors. Notably, AI methods overtake k-mer methods only in the top quartile of training-set size, indicating that data scale, not architecture, drives the recent dominance of deep models. KDM provides a single interpretable representation across the full motif-analysis workflow.

bioinformatics↗

RNAMaRs: an interpretable framework for inferring multivalent RNA Motifs and cognate Regulators of Splicing

Alternative splicing expands proteomic diversity and is shaped by interactions between RNA-binding proteins (RBPs) and multivalent RNA motifs. Linking sequence elements to regulatory proteins remains difficult from sequence information alone. Here we present RNAMaRs, a interpretable statistical framework that combines motif discovery with in vivo binding and splicing responses to infer motif-RBP relationships. RNAMaRs learns RBP binding principles, weights signal quality, and optimizes motif discovery in an RBP-specific manner. Across ENCODE datasets RNAMaRs consistently prioritizes the perturbed regulator, especially for large splicing effects. Independent validation in prostate cancer cells recapitulates HNRNPK binding signatures, supporting transferability across an unseen cellular context.

molecular biology↗