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Biology subjects

Gruening, B.

Publications and source records attributed to Gruening, B..

17 recordsLinked to original sources

Verifiable Agentic Science on Public Infrastructure

Autonomous artificial intelligence agents are transforming the practice of science. Across every discipline, researchers are handing data analysis to coding agents that can design and execute complex studies from a single prompt. Yet this revolution carries a threat. When agents improvise in local environments, they leave no verifiable record, ultimately risking a wave of irreproducible science. Solving this crisis requires moving agentic science onto public infrastructure where every action leaves an examinable trail. Here we connect autonomous coding agents to shared computing resources, turning ephemeral prompts into auditable scientific records. After showing that 30 unguided local agents splinter into 18 incompatible pipelines on the same dataset, we conduct an agentic reproduction and discovery study on a large scale---reproducing a large, diverse array of studies with every workflow, history, and intermediate dataset publicly accessible. This complete provenance trail exposes unstated modeling choices, reference mismatches, and subsampled tutorial inputs in published studies, and establishes a new foundation where human scientists can understand, steer, and trust AI-driven discovery.

bioinformatics↗

Prioritizing DNA methylation biomarkers using graph neural networks and explainable AI

DNA methylation is a significant epigenetic modification involving the addition of a methyl group to the position 5' of the cytosine residues. The modification is responsible for disease progression, immune response, and outcomes in diseases such as breast cancer (BC) and acute myeloid leukemia (AML). Illuminas HumanMethylation450 BeadChip (450K) and EPIC BeadChip (850K) methylation arrays are heavily used for such cancer studies to determine differentially expressed and differentially methylated genomic regions. Many of these are biomarkers used effectively for exploring therapeutic targets. Several studies report a few potential biomarkers, but the enormous numbers of largely unexplored probe-level (CpG sites) methylation signals may contain additional significant biomarkers. To prioritise the under-explored and disease-specific CpG sites from DNA methylation arrays and potentially uncover novel biomarkers, we present the novel approach GraphMeX-plain, a graph neural network (GNN)-based approach with explainable AI module. The underlying graph neural network is a principal neighbourhood aggregation (PNA). The approach uses the biomarkers reported in recent studies to rank biomarkers from the unexplored set. A similarity graph between CpG sites (known and unexplored sets) is constructed using DNA methylation {beta} values from arrays, producing an interaction graph. Biomarkers from recent studies are used as seeds and from the unexplored CpG sites, highly-variable ones (excluding the seeds) are selected that vary significantly between conditions (BC patients and normal controls for breast cancer arrays). Using the combination of seed and highly-variable CpG sites, a positive-unlabeled approach, network-informed adaptive positive-unlabeled learning (NIAPU), is utilized to assign a set of soft labels to unknown CpG sites such as likely positive, weakly negative, likely negative, and reliable negative in the descending order of likelihood of CpG sites being potential biomarkers. The graph neural network, a multi-layer PNA, refines the soft label assignments and achieves a high F1 classification score (weighted) of 0.93 for BC and 0.91 for AML. The most likely set of CpG sites, classified under "likely positive", are further explored using GNNExplainer, an explainable AI approach. Subgraphs for likely positive CpG sites, predicted with high probabilities, are computed and their proximities to the original seed CpG sites are analysed. The CpG sites which are predicted as likely positives have close interactions to the seeds. The top likely positive CpG site for BC is cg13265740 (C6orf115) where gene C6orf115 is strongly associated with BC. For AML, the top likely positive predicted CpG site is cg23281527 (KLHDC7A) where gene KLHDC7A plays a strong role in the mechanism of AML. A high percentage of these likely positive predicted CpG sites for both BC and AML, which remained unseen by the GNN model during training, are highly relevant to them and can serve as potential therapeutic targets and prognostic values.

bioinformatics↗

microGalaxy: A gateway to tools, workflows, and training for reproducible and FAIR analysis of microbial data

The explosion of microbial omics data has outpaced the ability of many researchers to analyze it, with complex tools and limited computational resources creating barriers to discovery. To address this gap, we present the Microbiology Galaxy Lab: a free, globally accessible, community-supported platform that combines state-of-the-art analytical power with user-friendly accessibility. Supported by the Galaxy and global microbiology communities, this platform integrates over 315 tool suites and 115 curated workflows, enabling comprehensive metabarcoding, (meta)genomic, (meta)transcriptomic, and (meta)proteomic data analysis within a FAIR-aligned environment. It also supports research in the health and infectious disease sectors, as well as in environmental microbiology. The platforms utility is exemplified through various use cases, including antimicrobial resistance tracking, biomarker prediction, microbiome classification, and functional annotation of key microbes. Built on reproducibility and community engagement, it supports creation, sharing, and updating of best-practice workflows. Over 35 tutorials and learning paths empower scientists, fostering an ecosystem that keeps resources at the forefront of microbial science. The Microbiology Galaxy Lab enables collective analysis, democratising research, thereby accelerating discovery across the global microbiology community (microbiology.usegalaxy.org, microbiology.usegalaxy.eu, microbiology.usegalaxy.org.au, microbiology.usegalaxy.fr).

bioinformatics↗

varVAMP: automated pan-specific primer design for tiled full genome sequencing and qPCR of highly diverse viral pathogens.

Time- and cost-saving surveillance of viral pathogens is achieved by tiled sequencing in which a viral genome is amplified in overlapping PCR amplicons and qPCR. However, designing pan-specific primers for viral pathogens that have high genomic variability represents a major challenge. Here, we present a bioinformatics command-line tool, called varVAMP (variable virus amplicons). It relies on multiple sequence alignments of highly variable virus sequences and enables automatic pan-specific primer design for qPCR or tiled amplicon whole genome sequencing. The varVAMP software guarantees pan-specificity by two means: it designs primers in regions with minimal variability and introduces degenerate nucleotides into primer sequences to compensate for common sequence variations. We demonstrate varVAMPs utility by designing and evaluating novel pan-specific primer schemes suitable for sequencing the genomes of SARS-CoV-2, Hepatitis E virus, rat Hepatitis E virus, Hepatitis A virus, Borna-disease-virus-1, and Poliovirus. Moreover, we established highly sensitive and specific Poliovirus qPCR assays that could potentially simplify current Poliovirus surveillance. Importantly, wet-lab and bioinformatic techniques established for SARS-CoV-2 tiled amplicon sequencing were readily transferable to these new primer schemes and will allow sequencing laboratories to extend their established methodology to other human pathogens.

bioinformatics↗

Activator-blocker model of transcriptional regulation by pioneer-like factors

Zygotic genome activation (ZGA) in the development of flies, fish, frogs and mammals depends on pioneer-like transcription factors (TFs). Those TFs create open chromatin regions, promote histone acetylation on enhancers, and activate transcription. Here, we use the panel of single, double and triple mutants for zebrafish genome activators Pou5f3, Sox19b and Nanog, multi-omics and mathematical modeling to investigate the combinatorial mechanisms of genome activation. We show that Pou5f3 and Nanog act differently on synergistic and antagonistic enhancer types. Pou5f3 and Nanog both bind as pioneer-like TFs on synergistic enhancers, promote histone acetylation and activate transcription. Antagonistic enhancers are activated by binding of one of these factors. The other TF binds as non-pioneer-like TF, competes with the activator and blocks all its effects, partially or completely. This activator-blocker mechanism mutually restricts widespread transcriptional activation by Pou5f3 and Nanog and prevents premature expression of late developmental regulators in the early embryo.

developmental biology↗

Transformer-based tool recommendation system in Galaxy

Galaxy is a web-based open-source platform for scientific analyses. Researchers use thousands of high-quality tools and workflows for their respective analyses. Tool recommender system predicts a collection of tools that can be used to extend an analysis. In this work, a tool recommender system is developed by training a Transformer-based neural network on workflows available on Galaxy Europe. Compared to the existing tool recommender system on Galaxy Europe that trains a recurrent neural network, the transformer-based neural network achieves two times faster convergence, has a four times lower model usage (model loading + prediction) time and shows a better generalisation that goes beyond training workflows. The scripts to create the recommendation model are available under MIT licence at https://github.com/anuprulez/galaxy_tool_recommendation_transformers.

bioinformatics↗

An accessible infrastructure for artificial intelligence using a docker-based Jupyterlab in Galaxy

Artificial intelligence (AI) programs that train on a large amount of data require powerful compute infrastructure. Jupyterlab notebook provides an excellent framework for developing AI programs but it needs to be hosted on a powerful infrastructure to enable AI programs to train on large data. An open-source, docker-based, and GPU-enabled jupyterlab notebook infrastructure has been developed that runs on the public compute infrastructure of Galaxy Europe for rapid prototyping and developing end-to-end AI projects. Using such a notebook, long-running AI model training programs can be executed remotely. Trained models, represented in a standard open neural network exchange (ONNX) format, and other resulting datasets are created in Galaxy. Other features include GPU support for faster training, git integration for version control, the option of creating and executing pipelines of notebooks, and the availability of multiple dashboards for monitoring compute resources. These features make the jupyterlab notebook highly suitable for creating and managing AI projects. A recent scientific publication that predicts infected regions of COVID-19 CT scan images is reproduced using multiple features of this notebook. In addition, colabfold, a faster implementation of alphafold2, can also be accessed in this notebook to predict the 3D structure of protein sequences. Jupyterlab notebook is accessible in two ways - first as an interactive Galaxy tool and second by running the underlying docker container. In both ways, long-running training can be executed on Galaxys compute infrastructure. The scripts to create the docker container are available under MIT license at https://github.com/anuprulez/ml-jupyter-notebook. Contactkumara@informatik.uni-freiburg.de anup.rulez@gmail.com

bioinformatics↗

Democratizing Data-Independent Acquisition Proteomics Analysis on Public Cloud Infrastructures Via The Galaxy Framework

Data-independent acquisition (DIA) has become an important approach in global, mass spectrometric proteomic studies because it provides in-depth insights into the molecular variety of biological systems. However, DIA data analysis remains challenging due to the high complexity and large data and sample size, which require specialized software and large computing infrastructures. Most available open-source DIA software necessitate basic programming skills and cover only a fraction of the analysis steps, often yielding a complex of multiple software tools, severely limiting usability and reproducibility. To overcome this hurdle, we have integrated a suite of DIA tools in the Galaxy framework for reproducible and version-controlled data processing. The DIA suite includes OpenSwath, PyProphet, diapysef and swath2stats. We have compiled functional Galaxy pipelines for DIA processing, which provide a web-based graphical user interface to these pre-installed and pre-configured tools for their usage on freely accessible, powerful computational resources of the Galaxy framework. This approach also enables seamless sharing workflows with full configuration in addition to sharing raw data and results. We demonstrate usability of the all-in-one DIA pipeline in Galaxy by the analysis of a spike-in case study dataset. Additionally, extensive training material is provided, to further increase access for the proteomics community.

bioinformatics↗

Loop detection using Hi-C data with HiCExplorer

Chromatin loops are an important factor in the structural organization of the genome. The detection of chromatin loops in Hi-C interaction matrices is a challenging and compute intensive task. The presented approach shows a chromatin loop detection algorithm which applies a strict candidate selection based on continuous negative binomial distributions and performs a Wilcoxon rank-sum test to detect enriched Hi-C interactions.

bioinformatics↗

Approximate k-nearest neighbors graph for single-cell Hi-C dimensional reduction with MinHash

Single-cell Hi-C interaction matrices are high dimensional and very sparse. To cluster thousands of single-cell Hi-C interaction matrices they are flattened and compiled into one matrix. This matrix can, depending on the resolution, have a few millions or even billions of features and any computation with it is therefore memory demanding. A common approach to reduce the number of features is to compute a nearest neighbors graph. However, the exact euclidean distance computation is in O(n2) and therefore we present an implementation of an approximate nearest neighbors method based on local sensitive hashing running in O(n). The presented method is able to process a 10kb single-cell Hi-C data set with 2500 cells and needs 53 GB of memory while the exact k-nearest neighbors approach is not computable with 1 TB of memory.

bioinformatics↗

Tool recommender system in Galaxy using deep learning

Galaxy is a web-based and open-source scientific data-processing platform. Researchers compose pipelines in Galaxy to analyse scientific data. These pipelines, also known as workflows, can be complex and difficult to create from thousands of tools, especially for researchers new to Galaxy. To make creating workflows easier, faster and less error-prone, a predictive system is developed to recommend tools facilitating further analysis. A model is created to recommend tools by analysing workflows, composed by researchers on the European Galaxy server, using a deep learning approach. The higher-order dependencies in workflows, represented as directed acyclic graphs, are learned by training a gated recurrent units (GRU) neural network, a variant of a recurrent neural network (RNN). The weights of tools used in the neural network training are derived from their usage frequencies over a period of time. The hyper-parameters of the neural network are optimised using Bayesian optimisation. An accuracy of 97% in predicting tools is achieved by the model for precision@1, precision@2 and precision@3 metrics. It is accessed by a Galaxy API to recommend tools in real-time. Multiple user interface (UI) integrations on the server communicate with this API to apprise researchers of these recommended tools interactively. Contactkumara@informatik.uni-freiburg.de gruening@informatik.uni-freiburg.de backofen@informatik.uni-freiburg.de

bioinformatics↗

Accessible and reproducible mass spectrometry imaging data analysis in Galaxy

BackgroundMass spectrometry imaging is increasingly used in biological and translational research as it has the ability to determine the spatial distribution of hundreds of analytes in a sample. Being at the interface of proteomics/metabolomics and imaging, the acquired data sets are large and complex and often analyzed with proprietary software or in-house scripts, which hinder reproducibility. Open source software solutions that enable reproducible data analysis often require programming skills and are therefore not accessible to many MSI researchers.\n\nFindingsWe have integrated 18 dedicated mass spectrometry imaging tools into the Galaxy framework to allow accessible, reproducible, and transparent data analysis. Our tools are based on Cardinal, MALDIquant, and scikit-image and enable all major MSI analysis steps such as quality control, visualization, preprocessing, statistical analysis, and image co-registration. Further, we created hands-on training material for use cases in proteomics and metabolomics. To demonstrate the utility of our tools, we re-analyzed a publicly available N-linked glycan imaging dataset. By providing the entire analysis history online, we highlight how the Galaxy framework fosters transparent and reproducible research.\n\nConclusionThe Galaxy framework has emerged as a powerful analysis platform for the analysis of MSI data with ease of use and access together with high levels of reproducibility and transparency.

bioinformatics↗

Empowering the annotation and discovery of structured RNAs with scalable and accessible integrative clustering

RNA plays essential regulatory roles in all known forms of life. Clustering RNA sequences with common sequence and structure is an essential step towards studying RNA function. With the advent of high-throughput sequencing techniques, experimental and genomic data are expanding to complement the predictive methods. However, the existing methods do not effectively utilize and cope with the immense amount of data becoming available. Here we present GraphClust2, a comprehensive approach for scalable clustering of RNAs based on sequence and structural similarities. GraphClust2 provides an integrative solution by incorporating diverse types of experimental and genomic data in an accessible fashion via the Galaxy framework. We demonstrate that the tasks of clustering and annotation of structured RNAs can be considerably improved, through a scalable methodology that also supports structure probing data. Based on this, we further introduce an off-the-shelf procedure to identify locally conserved structure candidates in long RNAs. In this way, we suggest the presence and the sparsity of phylogenetically conserved local structures in some long non-coding RNAs. Furthermore, we demonstrate the advantage of a scalable clustering for discovering structured motifs under inherent and experimental biases and uncover prominent targets of the double-stranded RNA binding protein Roquin-1 that are evolutionary conserved.

bioinformatics↗

Galaxy-Kubernetes integration: scaling bioinformatics workflows in the cloud

Making reproducible, auditable and scalable data-processing analysis workflows is an important challenge in the field of bioinformatics. Recently, software containers and cloud computing introduced a novel solution to address these challenges. They simplify software installation, management and reproducibility by packaging tools and their dependencies. In this work we implemented a cloud provider agnostic and scalable container orchestration setup for the popular Galaxy workflow environment. This solution enables Galaxy to run on and offload jobs to most cloud providers (e.g. Amazon Web Services, Google Cloud or OpenStack, among others) through the Kubernetes container orchestrator. AvailabilityAll code has been contributed to the Galaxy Project and is available (since Galaxy 17.05) at https://github.com/galaxyproject/ in the galaxy and galaxy-kubernetes repositories. https://public.phenomenal-h2020.eu/ is an example deployment. Suppl. InformationSupplementary Files are available online. Contactpmoreno@ebi.ac.uk, European Molecular Biology Laboratory, EMBL-EBI, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SD, UK, Tel: +44-1223-494267, Fax: +44-1223-484696.

bioinformatics↗

Pou5f3, SoxB1 and Nanog remodel chromatin on High Nucleosome Affinity Regions at Zygotic Genome Activation

The zebrafish embryo is mostly transcriptionally quiescent during the first 10 cell cycles, until the main wave of Zygotic Genome Activation (ZGA) occurs, accompanied by fast chromatin remodeling. At ZGA, homologs of mammalian stem cell transcription factors (TFs) Pou5f3, Nanog and Sox19b bind to thousands of developmental enhancers to initiate transcription. So far, how these TFs influence chromatin dynamics at ZGA has remained unresolved. To address this question, we analyzed nucleosome positions in wild-type and Maternal-Zygotic (MZ) mutants for pou5f3 and nanog by MNase-seq. We show that Nanog, Sox19b and Pou5f3 bind to the High Nucleosome Affinity Regions (HNARs). HNARs are spanning over 600 bp, featuring high in vivo and predicted in vitro nucleosome occupancy and high predicted propeller twist DNA shape value. We suggest a two-step nucleosome destabilization-depletion model, where the same intrinsic DNA properties of HNAR promote both high nucleosome occupancy and differential binding of TFs. In the first step, already prior to ZGA, Pou5f3 and Nanog destabilize nucleosomes on HNAR centers genome-wide. In the second step, post-ZGA, Nanog, Pou5f3 and SoxB1 maintain open chromatin state on the subset of HNARs, acting synergistically. Nanog binds to the HNAR center, while the Pou5f3 stabilizes the flanks. The HNAR model will provide a useful tool for genome regulatory studies in the variety of biological systems.

developmental biology↗

Parkour LIMS: facilitating high-quality sample preparation in next generation sequencing

SummaryThis paper presents Parkour, a software package for sample processing and quality management of next generation sequencing data and samples. Starting with user requests, Parkour allows tracking and assessing samples based on predefined quality criteria through different stages of the sample preparation workflow. Ideally suited for academic core laboratories, the software aims to maximize efficiency and reduce turnaround time by intelligent sample grouping and a clear assignment of staff to work units. Tools for automated invoicing, interactive statistics on facility usage and simple report generation minimize administrative tasks. Provided as a web application, Parkour is a convenient tool for both deep sequencing service users and laboratory personal. A set of web APIs allow coordinated information sharing with local and remote bioinformaticians. The flexible structure allows workflow customization and simple addition of new features as well as the expansion to other domains.\n\nAvailability and implementationThe code and documentation are available at https://github.com/maxplanck-ie/parkour\n\nContactboenisch@ie-freiburg.mpg.de

genomics↗

Strategies for analyzing bisulfite sequencing data

DNA methylation is one of the main epigenetic modifications in the eukaryotic genome; it has been shown to play a role in cell-type specific regulation of gene expression, and therefore cell-type identity. Bisulfite sequencing is the gold-standard for measuring methylation over the genomes of interest. Here, we review several techniques used for the analysis of high-throughput bisulfite sequencing. We introduce specialized short-read alignment techniques as well as pre/post-alignment quality check methods to ensure data quality. Furthermore, we discuss subsequent analysis steps after alignment. We introduce various differential methylation methods and compare their performance using simulated and real bisulfite sequencing datasets. We also discuss the methods used to segment methylomes in order to pinpoint regulatory regions. We introduce annotation methods that can be used for further classification of regions returned by segmentation and differential methylation methods. Finally, we review software packages that implement strategies to efficiently deal with large bisulfite sequencing datasets locally and we discuss online analysis workflows that do not require any prior programming skills. The analysis strategies described in this review will guide researchers at any level to the best practices of bisulfite sequencing analysis.

bioinformatics↗