Search bioRxivSearch

bioRxiv · 10.1101/155150

Not All Experimental Questions Are Created Equal: Accelerating Biological Data to Knowledge Transformation (BD2K) via Science Informatics, Active Learning and Artificial Intelligence

Abstract

Pablo Picasso, when first told about computers, famously quipped \"Computers are useless. They can only give you answers.\" Indeed, the majority of effort in the first half-century of computational research has focused on methods for producing answers. Incredible progress has been achieved in computational modeling, simulation and optimization, across domains as diverse as astrophysics, climate studies, biomedicine, architecture, and chess. However, the use of computers to pose new questions, or prioritize existing ones, has thus far been quite limited.\n\nPicassos comment highlights the point that good questions can sometimes be more elusive than good answers. The history of science offers numerous examples of the impact of good questions. Paul Erd[o]s, the wandering monk of mathematical graph theory, offered small prizes for anyone who could prove conjectures he identified as important (1). The prizes varied in cash amounts based on the perceived complexity of the problem posed by Erd[o]s.\n\nPosing technical questions and allocating resources to answer them has taken on a new guise in the Internet age. The X-Prize foundation (http://www.xprize.org/) offers multi-million dollar bounties for grand technological goals, including goals for sequencing genomes or space exploration. Several companies provide portals where customers can place cash bounties on educational, scientific or technological challenges, while potential problem solvers can compete to produce the best solutions for these problems. Amazons Turk site (https://www.mturk.com/mturk/welcome) links people requesting performance of intellectual tasks to people willing to work on them for a fee. Such crowd-sourcing systems create markets of questions and answers, and can help allocate resources and capabilities efficiently.\n\nThis paradigm suggests a number of interesting questions for scientific research. In a resource limited environment, can funds and research capacity be allocated more efficiently? Can knowledge demand provide an alternative or complementary mechanism to traditional investigator-initiated research grants?\n\nThe fathers of Artificial Intelligence (AI) and Herbert Simon in particular envisioned the application of AI to Scientific Discovery in different forms and styles (focusing on physics). We follow on these early dreams and describe a novel approach aimed at remodeling of the biomedical research infrastructure and catalyze gene function determination. We aim to start a bold discussion of new ideas aimed towards increasing the efficiency of the allocation of research capacities, reproducibility, provenance tracking, removing redundancy and catalyzing knowledge gain with each experiment. In particular, we describe a tractable computational framework and infrastructure that can help researchers assess the potential information gain of millions of experiments before conducting them. The utility of experiments in this case is modeled as the predictive knowledge (formalized as information) to be gained as a result of performing the experiment. The experimentalist would then be empowered to select experiments that maximized information gain if they wished, recognizing that there are frequently other considerations, such as a specific technological or medical utility, that might over-ride the priority of maximizing information gain. The conceptual approach we develop is general, and here we apply it to the study of gene function.

Explore related subjects

Keep this discovery

BibTeXRIS

Kasif, S., Letovsky, S., Roberts, R. J., Steffen, M.. 2017-06-25. Not All Experimental Questions Are Created Equal: Accelerating Biological Data to Knowledge Transformation (BD2K) via Science Informatics, Active Learning and Artificial Intelligence. https://doi.org/10.1101/155150

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

spatialMET: an open and scalable framework for spatial metabolomics analysis

Mass spectrometry imaging (MSI) enables spatially resolved metabolomics in intact tissue sections, but analysis remains challenging at scale. Existing MSI workflows often require users to combine multiple software tools, while others rely on proprietary vendor software that limits interoperability and reproducibility. To address these challenges, we developed spatialMET, an open-source framework that provides an end-to-end workflow for MSI analysis. spatialMET provides a unified platform for preprocessing, spatial domain detection, and visualization. Downstream analyses include differential abundance testing, spatial autocorrelation and gradient analysis, dimensionality reduction, and correlation network analysis. Spatial domain detection uses hcdist, a C-based hierarchical clustering implementation that substantially reduces runtime and memory use relative to existing R-based approaches. spatialMET can be run through an interactive R Shiny application or as a standalone command-line workflow for larger datasets or high-performance computing environments. Applied to mouse small cell lung cancer MALDI-MSI data containing 284,673 pixels, spatialMET identified tumor-associated, stromal, and adjacent lung spatial domains that aligned with matched histology. Differential abundance analysis identified 117 m/z features that differed between tumor and stromal regions, while spatial autocorrelation analyses revealed spatially structured abundance patterns. Applying spatialMET to mouse lung adenocarcinoma data from an entire lung lobe containing 338,477 pixels further demonstrated scalability and captured spatial heterogeneity across tumor and surrounding lung tissue. In summary, spatialMET provides a scalable, open-source framework for end-to-end spatial metabolomics analysis, and it is distributed as a Docker container for reproducible deployment. Source code and installation instructions are available at https://github.com/biodatalab/spatialMET.

bioinformatics

Probing the transcriptome response to shivering in skeletal muscle using a multilayered bioinformatics approach

Cold acclimation holds therapeutic potential for improving metabolic health. We previously demonstrated that repeated cold-induced shivering enhances insulin sensitivity in humans. However, the molecular pathways that underlie the skeletal muscle shivering response, and how these relate to beneficial physiological effects, remain poorly understood. In this study, we combined complementary bioinformatics approaches to allow in-depth analysis of the transcriptomic response of human skeletal muscle to repeated shivering. We identified a robust transcriptional signature and show a sex-specific component in the shivering skeletal muscle response, which seemed to diminish following cold adaptation. Our findings provide mechanistic insights into cold-induced muscle adaptations, shed light on potential interesting molecular targets for further investigation, and emphasize the importance of including both sexes in future cold acclimation studies.

bioinformatics

An Information Geometry approach to model topological trajectories and Gene Expression Radius from UMAP geometry.

Understanding the relationship between gene expression dynamics and cellular identity remains a central challenge in single cell biology. Here, we introduce a novel computational and mathematical framework that integrates information geometry, fuzzy topology, and UMAP analysis to model gene expression landscapes derived from single cell RNA sequencing data. We formalize gene expression data as a fuzzy topological space, where interactions between expression points are governed by probabilistic distributions inspired by manifold learning approaches such as UMAP. Within this framework, we define an information geometric structure through a Fisher metric induced by these distributions, enabling the computation of geodesic trajectories that capture cellular differentiation processes. A key contribution of this work is the derivation of analytical conditions, expressed as expression radius formulas, that characterize local neighborhoods in gene expression space. These conditions allow for the identification of genes associated with stem cell states and predictions in transitional cell types in future work. Application of the proposed framework to single cell datasets reveals biologically meaningful gene sets enriched in key regulatory pathways and transcription factors, demonstrating the capacity of our approach to uncover latent structure in complex gene expression data. Our results suggest that integrating differential geometry with statistical learning theory offers a powerful paradigm for modeling genotype and phenotype relationships and cellular state transitions, with potential implications for precision medicine and systems biology.

bioinformatics