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Zafeiropoulos, H.

Publications and source records attributed to Zafeiropoulos, H..

6 recordsLinked to original sources

μGrowthDB: querying, visualizing, and sharing microbial growth curve data

Microbial growth curve data contain valuable information about microorganisms physiology and metabolism. However, they are currently reported in various formats scattered across publications. A generic resource that allows querying and comparing microbial growth curve data is currently missing. For this reason, we developed GrowthDB, an open repository designed to store, visualize, analyze, and share quantitative measurements of species abundances and metabolite profiles from monocultures and communities of known composition. GrowthDB is designed to accommodate a range of experimental designs and measurement techniques. In addition to querying microbial growth curves by organism or metabolite, GrowthDB supports comparative visualisation of growth curves and offers a guided data submission process intended to make data upload as easy as possible. GrowthDB is available at: https://mgrowthdb.gbiomed.kuleuven.be/.

microbiology↗

microbetag: simplifying microbial network interpretation through annotation, enrichment tests and metabolic complementarity analysis

Microbial co-occurrence network inference is often hindered by low accuracy and tool dependency. We introduce microbetag, a comprehensive software ecosystem designed to enhance network annotation. Nodes (taxa) are enriched with phenotypic traits, while edges represent metabolic complementarities, highlighting potential cross-feeding relationships. microbetags online version relies on microbetagDB, a database of 34,608 high-quality genomes with detailed annotations. A stand-alone tool allows users to apply microbetag to custom reference genomes/bins/MAGs. Additionally, MGG, a CytoscapeApp, offers a streamlined, user-friendly interface for network retrieval and visualization. microbetag effectively identified known metabolic interactions and serves as a robust hypothesis-generating tool.

systems biology↗

A long-term ecological research data set from the marine genetic monitoring programme ARMS-MBON 2018-2020

Molecular methods such as DNA/eDNA metabarcoding have emerged as useful tools to document biodiversity of complex communities over large spatio-temporal scales. We established an international Marine Biodiversity Observation Network (ARMS-MBON) combining standardised sampling using autonomous reef monitoring structures (ARMS) with metabarcoding for genetic monitoring of marine hard-bottom benthic communities. Here, we present the data of our first sampling campaign comprising 56 ARMS units deployed in 2018-2019 and retrieved in 2018-2020 across 15 observatories along the coasts of Europe and adjacent regions. We describe the open-access data set (image, genetic, and metadata) and explore the genetic data to show its potential for marine biodiversity monitoring and ecological research. Our analysis shows that ARMS recovered more than 60 eukaryotic phyla capturing diversity of up to [~]5,500 amplicon sequence variants and [~]1,800 operational taxonomic units, and up to [~]250 and [~]50 species per observatory using the cytochrome c oxidase subunit I (COI) and 18S rRNA marker genes, respectively. Further, ARMS detected threatened, vulnerable and non-indigenous species often targeted in biological monitoring. We show that while deployment duration does not drive diversity estimates, sampling effort and sequencing depth across observatories do. We recommend that ARMS should be deployed for at least three to six months during the main growth season to use resources as efficiently as possible and that post-sequencing curation is applied to enable statistical comparison of spatio-temporal entities. We suggest that ARMS should be used in biological monitoring programmes and long-term ecological research and encourage the adoption of our ARMS-MBON protocols.

ecology↗

dingo: a Python package for metabolic flux sampling

SummaryWe present dingo, a Python package that supports a variety of methods to sample from the flux space of metabolic models, based on state-of-the-art random walks and rounding methods. For uniform sampling dingos implementation of the Multiphase Monte Carlo Sampling algorithm, provides a significant speed-up and outperforms existing software. Indicatively, dingo can sample from the flux space of the largest metabolic model up to now (Recon3D) in less than 30 hours using a personal computer, under several statistical guarantees; this computation is out of reach for other similar software. In addition, supports common analysis methods, such as Flux Balance Analysis (FBA) and Flux Variability Analysis (FVA), and visualization components. dingo contributes to the arsenal of tools in metabolic modeling by enabling flux sampling in high dimensions (in the order of thousands). Availability and implementationhttps://github.com/GeomScale/dingo Contacttolis.chal@gmail.gr, haris.zafeiropoulos@kuleuven.be

bioinformatics↗

Bacteria are everywhere, even in your COI marker gene data!

The mitochondrial cytochrome C oxidase subunit I gene (COI) is commonly used in eDNA metabarcoding studies, especially for assessing metazoan diversity. Yet, a great number of COI operational taxonomic units or/and amplicon sequence variants are retrieved from such studies and referred to as "dark matter", and do not get a taxonomic assignment with a reference sequence. For a thorough investigation of this dark matter, we have developed the Dark mAtteR iNvestigator (DARN) software tool. A reference COI-oriented phylogenetic tree was built from 1,240 consensus sequences covering all the three domains of life, with more than 80% of those representing eukaryotic taxa. With respect to eukaryotes, consensus sequences at the family level were constructed from 183,330 retrieved from the Midori reference 2 database. Similarly, sequences from 559 bacterial genera and 41 archaeal were retrieved from the BOLD database. DARN makes use of the phylogenetic tree to investigate and quantify pre-processed sequences of amplicon samples to provide both a tabular and a graphical overview of phylogenetic assignments. To evaluate DARN, both environmental and bulk metabarcoding samples from different aquatic environments using various primer sets were analysed. We demonstrate that a large proportion of non-target prokaryotic organisms such as bacteria and archaea are also amplified in eDNA samples and we suggest bacterial COI sequences to be included in the reference databases used for the taxonomy assignment to allow for further analyses of dark matter. DARN source code is available on GitHub at https://github.com/hariszaf/darn and you may find it as a Docker at https://hub.docker.com/r/hariszaf/darn. Author summaryDARN is a software approach aiming to provide further insight in the COI amplicon data coming from environmental samples. Building a COI-oriented reference phylogeny tree is a challenging task especially considering the small number of microbial curated COI sequences deposited in reference databases; e.g ~4,000 bacterial and ~150 archaeal in BOLD. Apparently, as more and more such sequences are collated, the DARN approach improves. To provide a more interactive way of communicating both our approach and our results, we strongly suggest the reader to visit this Google Collab notebook where all steps are described step by step and also this GitHub page where our results are demonstrated. Our approach corroborates the known presence of microbial sequences in COI environmental sequencing samples and highlights the need for curated bacterial and archaeal COI sequences and their integration into reference databases (i.e. Midori, BOLD, etc). We argue that DARN will benefit researchers as a quality control tool for their sequenced samples in terms of distinguishing eukaryotic from non-eukaryotic OTUs/ASVs, but also in terms of understanding the unknown unknowns.

bioinformatics↗

PEMA: from the raw .fastq files of 16S rRNA and COI marker genes to the (M)OTU-table, a thorough metabarcoding analysis

BackgroundEnvironmental DNA (eDNA) and metabarcoding, allow the identification of a mixture of individuals and launch a new era in bio- and eco-assessment. A number of steps are required to obtain taxonomically assigned (Molecular) Operational Taxonomic Unit ((M)OTU) tables from raw data. For most of these, a plethora of tools is available; each tools execution parameters need to be tailored to reflect each experiments idiosyncrasy. Adding to this complexity, for such analyses, the computation capacity of High Performance Computing (HPC) systems is frequently required.\n\nSoftware containerization technologies ease the sharing and running of software packages across operating systems; thus, they strongly facilitate pipeline development and usage. Likewise are programming languages specialized for big data pipelines, incorporating features like roll-back checkpoints and on-demand partial pipeline execution.\n\nFindingsPEMA is a containerized assembly of key metabarcoding analysis tools with a low effort in setting up, running and customizing to researchers needs. Based on third party tools, PEMA performs reads pre-processing, clustering to (M)OTUs and taxonomy assignment for 16S rRNA and COI marker gene data. Due to its simplified parameterisation and checkpoint support, PEMA allows users to explore alternative algorithms for specific steps of the pipeline without the need of a complete re-execution. PEMA was evaluated against previously published datasets and achieved comparable quality results.\n\nConclusionsGiven its time-efficient performance and its quality results, it is suggested that PEMA can be used for accurate eDNA metabarcoding analysis, thus enhancing the applicability of next-generation biodiversity assessment studies.

bioinformatics↗