Metal & Tolerance

9 projects
metal tolerance environmental resistance atlas

BacDive Isolation Environment × Metal Tolerance Prediction

Completed

Do bacteria isolated from metal-contaminated environments have higher predicted metal tolerance scores than bacteria from uncontaminated environments?

BacDive Phenotype Signatures of Metal Tolerance

Completed

Can BacDive-measured bacterial phenotypes (Gram stain, oxygen tolerance, metabolite utilization, enzyme activities) predict metal tolerance as measure...

Counter Ion Effects on Metal Fitness Measurements

Completed

When bacteria are exposed to metal salts (CoCl₂, NiCl₂, CuCl₂), how much of the observed fitness effect is caused by the metal cation versus the count...

Gene-Resolution Metal Cross-Resistance Across Diverse Bacteria

Completed

Is the genetic architecture of metal cross-resistance conserved across phylogenetically diverse bacteria, or is it rewired species by species?

Pan-Bacterial Metal Fitness Atlas

Completed

Across diverse bacteria subjected to genome-wide fitness profiling under metal stress, what is the genetic architecture of metal tolerance — is it enc...

Global Biogeography of Environmental Bacterial Metal Resistance and Spatial Sampling Gaps

Completed

Where on Earth are metal-resistant environmental bacteria most abundant, and where are the gaps in public metagenomic sampling that prevent us from kn...

Metal-Specific vs General Stress Genes in the Metal Fitness Atlas

Completed

Among the 12,838 metal-important genes identified by the Metal Fitness Atlas, which are specifically required for metal tolerance vs general stress su...

Metal Resistance Ecology: Phylogenetic Conservation vs. Environmental Selection

Completed

Do metal-resistance functions in the global microbiome reflect phylogenetic constraint (conserved in lineages) or environmental selection (enriched in...

Soil Metal Concentrations Drive Functional Gene Shifts in the Environmental Microbiome

Completed

Which microbial functional gene categories (COGs) are significantly associated with soil metal concentrations at global scale, and do these associatio...

Essential & Core

6 projects
essential core conserved conservation metabolome

Openness & Open

4 projects
openness open closed metabolic patterns

Metabolic & Capability

3 projects
metabolic capability dependency annotation gapfilling

Modules & Core

3 projects
modules core module functional conservation

Environmental & Environment

3 projects
environmental environment alphaearth embeddings ecotype

Resistance & Antibiotic

2 projects
resistance antibiotic prophage predict microbial

Subsurface & Clay

2 projects
subsurface clay confined deep phylum

Functional & Differentiation

2 projects
functional differentiation differ core category

Distribution & Berdl

2 projects
distribution berdl environmental core accessory

Environmental & Resistance

2 projects
environmental resistance resistome antimicrobial scale

Resistance & Antimicrobial

2 projects
resistance antimicrobial cost support networks

Field & Effects

2 projects
field effects under predict ridge

Core & Paradox

2 projects
core paradox burdensome likely positive

Explorer & Kescience

2 projects
explorer kescience collection contain organisms

Dark & Them

2 projects
dark them unknown after annotation

Independent Studies

27 projects

Acinetobacter baylyi ADP1 Data Explorer

Completed

What is the scope and structure of a comprehensive ADP1 database, and how do its annotations, metabolic models, and phenotype data intersect with BERD...

ADP1 Deletion Collection Phenotype Analysis

Completed

What is the condition-dependent structure of gene essentiality in *Acinetobacter baylyi* ADP1, as revealed by the de Berardinis single-gene deletion c...

ADP1 Triple Essentiality Concordance

In Progress

Among genes that TnSeq says are dispensable in *Acinetobacter baylyi* ADP1, does FBA correctly predict which ones have growth defects? Can direct muta...

AlphaFold MSA Depth as a Lens on the Bacterial Annotation Gap

Completed

Does AlphaFold MSA depth predict functional annotation richness in the bacterial pangenome, and is structural novelty (low MSA depth) systematically e...

Within-Species AMR Strain Variation

Completed

Within a species, how does the AMR repertoire vary between strains, and what drives that variation?

Aromatic Catabolism Support Network in ADP1

Completed

Why does aromatic catabolism in *Acinetobacter baylyi* ADP1 require Complex I (NADH dehydrogenase), iron acquisition, and PQQ biosynthesis when growth...

BERDL Data Atlas — Inventory, Topic Map, and Cross-Reference Synergies

Completed

What data is available in BERDL (across tenants, agencies, and programs), what biological topics does it cover, and where do datasets amplify each oth...

Caulobacter Fur–Lipid A Loss

In Progress

Why does inactivation of *fur* (the ferric uptake regulator) permit the loss of lipid A in *Caulobacter crescentus*, when no equivalent connection to ...

CF Protective Microbiome Formulation Design

In Progress

Can we build a multi-criterion framework that explains measured *P. aeruginosa* PA14 inhibition from metabolic competition, growth kinetics, and patie...

ENIGMA Carbon Census 1

Completed

For 83 groundwater- and necromass-derived carbon compounds proposed for community enrichment and isolate phenotyping, what is known about (1) their en...

Contamination Gradient vs Functional Potential in ENIGMA Communities

Completed

Do high-contamination Oak Ridge groundwater communities show enrichment for taxa with higher inferred stress-related functional potential compared wit...

SSO Subsurface Community Ecology — Spatial Structure, Functional Gradients, and Hydrogeological Drivers

Completed

Does 16S community similarity across the 9 ENIGMA SSO wells (3x3 grid, ~4 m span at Oak Ridge) recapitulate the spatial arrangement in X, Y, and Z? Wh...

Metabolic Consistency of Pseudomonas FW300-N2E3

Completed

For *Pseudomonas fluorescens* FW300-N2E3 (ENIGMA groundwater isolate), how consistent are exometabolomic outputs (Web of Microbes), genome-wide gene f...

Gene Function Ecological Agora

Completed

Across the prokaryotic tree (GTDB r214; 293,059 genomes / 27,690 species), build a multi-resolution **innovation + acquisition-depth atlas of bacteria...

Genotype × Condition → Phenotype Prediction from ENIGMA Growth Curves

In Progress

Can we predict bacterial growth phenotype — at multiple resolutions from binary growth through continuous kinetics to complex dynamics — from genome c...

Harvard Forest Long-Term Warming — DNA vs RNA Functional Response

Completed

After ~25 years of +5°C experimental soil warming at the Harvard Forest Barre Woods plot, does the functional transcript pool (metatranscriptome KO/Pf...

Metagenome-Prioritized Phage Cocktails for Crohn's Disease and IBD

Completed

Which bacterial pathobionts are **enriched, ubiquitous, and non-protective** in IBD, UC, and Crohn's disease patients — considered both across indicat...

Lanthanide Methylotrophy Atlas

Completed

Across BERDL's 293K-genome pangenome, what is the phylogenomic distribution and cassette-completeness of the lanthanide-dependent methanol/ethanol oxi...

Lignin Enrichment and Ecological Memory in Microbial Communities

Completed

How does sequential enrichment on lignin, with or without labile carbon supplementation, shape bacterial and fungal community composition — and does e...

Community Metabolic Ecology via NMDC × Pangenome Integration

Completed

Do the GapMind-predicted pathway completeness profiles of community resident taxa predict or correlate with observed metabolomics profiles in NMDC env...

Polyhydroxybutyrate Granule Formation Pathways: Distribution Across Clades and Environmental Selection

Completed

How are polyhydroxybutyrate (PHB) granule-forming pathways distributed across bacterial clades and environments, and does this distribution support th...

Plant Microbiome Ecotypes

Completed

What is the genomic basis for plant-microbe associations across different plant compartments (rhizosphere, root, phyllosphere, endophyte)? Can we clas...

Prophage Gene Modules and Terminase-Defined Lineages Across Bacterial Phylogeny and Environmental Gradients

Completed

How are prophage gene modules and terminase-defined prophage lineages distributed across bacterial phylogeny and environmental gradients, and which mo...

Carbon Source Utilization Predicts Ecology and Lifestyle in Pseudomonas

Completed

Among free-living *Pseudomonas* clades, does the carbon source utilization profile predict the soil ecosystem type from which strains were isolated — ...

Condition-Specific Respiratory Chain Wiring in ADP1

Completed

How is *Acinetobacter baylyi* ADP1's branched respiratory chain wired across carbon sources — which NADH dehydrogenases and terminal oxidases are requ...

Soil Microbial Dark Matter: Genomic Frontiers and the Clay Shield Null Result

Completed

T4SS-CAZy Environmental HGT: Cross-Phylum Transfer of Carbohydrate-Active Enzyme Cassettes

Completed

Do Type IV secretion systems (T4SS) in environmental bacteria physically co-localise with carbohydrate-active enzyme (CAZy) genes in a manner consiste...