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JAFARI, M.

Publications and source records attributed to JAFARI, M..

2 recordsLinked to original sources

SOORENA: Self-lOOp containing or autoREgulatory Nodes in biological network Analysis

Autoregulatory mechanisms, in which proteins regulate their own activity or expression, are fundamental to biological networks but are challenging to identify systematically from literature. To address this gap, we present SOORENA (https://soorena.it.helsinki.fi/soorena/), a two-stage transformer model that predicts and classifies protein autoregulation in PubMed abstracts. SOORENA was trained on 1,332 experimentally validated abstracts and achieved 96.0 percent accuracy and 97.8 percent precision in stage one, with stage two achieving 95.5 percent accuracy and 96.2 percent macro-F1 across seven mechanistic classes. Applied to 3.34 million abstracts, SOORENA identified 85,145 publications containing autoregulatory mechanisms, yielding 97,657 protein-specific records. Integration with curated databases generated 100,065 comprehensive entries accessible via an interactive Shiny application. By systematically cataloging self-regulatory interactions, which often act as bottlenecks in dynamic network modeling, SOORENA provides a resource that supports mechanistic interpretation, model reduction, and predictive systems-level analyses. These results demonstrate that domain-specific language models can scale the discovery and curation of biologically essential self-regulatory mechanisms, bridging literature mining and systems biology.

bioinformatics↗

Missing Values Are Valuable: Shifting Focus from Amount to Form of Missing Data

Missing data is often treated as a nuisance, routinely imputed or excluded from statistical analyses, especially in nominal datasets where its structure cannot be easily modeled. However, the form of missingness itself can reveal hidden relationships, substructures, and biological or operational constraints within a dataset. In this study, we present a graph-theoretic approach that reinterprets missing values not as gaps to be filled, but as informative signals. By representing nominal variables as nodes and encoding observed or missing associations as edges, we construct both weighted and unweighted bipartite graphs to analyze modularity, nestedness, and projection-based similarities. This framework enables downstream clustering and structural characterization of nominal data based on the topology of observed and missing associations; edge prediction via multiple imputation strategies is included as an optional downstream analysis to evaluate how well inferred values preserve the structure identified in the non-missing data. Across a series of biological, ecological, and social case studies, including proteomics data, the BeatAML drug screening dataset, ecological pollination networks, and HR analytics, we demonstrate that the structure of missing values can be highly informative. These configurations often reflect meaningful constraints and latent substructures, providing signals that help distinguish between data missing at random and not at random. When analyzed with appropriate graph-based tools, these patterns can be leveraged to improve the structural understanding of data and provide complementary signals for downstream tasks such as clustering and similarity analysis. Our findings support a conceptual shift: missing values are not merely analytical obstacles but valuable sources of insight that, when properly modeled, can enrich our understanding of complex nominal systems across domains. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=107 SRC="FIGDIR/small/670516v2_ufig1.gif" ALT="Figure 1"> View larger version (24K): org.highwire.dtl.DTLVardef@99c5eaorg.highwire.dtl.DTLVardef@1909d8corg.highwire.dtl.DTLVardef@1578c93org.highwire.dtl.DTLVardef@ce2e90_HPS_FORMAT_FIGEXP M_FIG C_FIG Shiny app address https://ehsan-zangene.shinyapps.io/nimaa_app/

bioinformatics↗