William L. Trimble
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
William L. Trimble has a total of 170 co-authors. Here are the top co-authors by number of shared publications:
- Folker Meyer
Institute for AI in Medicine, University Hospital Essen, University of Duisburg-Essen, Essen, Germany
16 shared publications S. Gulick
Department of Physics, McGill University, Montreal, Quebec H3A 2T8, Canada
10 shared publicationsF. Buchinger
Department of Physics, McGill University, Montreal, Quebec H3A 2T8, Canada
9 shared publicationsG. Savard
Physics Division, Argonne National Laboratory, Argonne, Illinois 60439, USA
9 shared publicationsZ. Zhou
Physics Division, Argonne National Laboratory, Argonne, Illinois 60439, USA
8 shared publicationsJ. Vaz
Physics Division, Argonne National Laboratory, Argonne, IL 60439, USA
7 shared publications
Latest Publications
- Open Access
- 8 November 2019
- Published by Springer Nature in BMC Bioinformatics
- Vol. 20 (1) , 1-8
The MG-RAST API explorer: an on-ramp for RESTful query composition
Background: The MG-RAST API provides search capabilities and delivers organism and function data as well as raw or annotated sequence data via the web interface and its RESTful API. For casual users, however, RESTful APIs are hard to learn and work with. Results: We created the graphical MG-RAST API explorer to help researchers more easily build and export API queries; understand the data abstractions and indices available in MG-RAST; and use the results presented in-browser for exploration, development, and debugging. Conclusions: The API explorer lowers the barrier to entry for occasional or first-time MG-RAST API users.
- 8 November 2019
- Published by Springer Nature in BMC Bioinformatics
- Vol. 20 (1) , 1-8
Open AccessThe MG-RAST API explorer: an on-ramp for RESTful query composition
Background: The MG-RAST API provides search capabilities and delivers organism and function data as well as raw or annotated sequence data via the web interface and its RESTful API. For casual users, however, RESTful APIs are hard to learn and work with. Results: We created the graphical MG-RAST API explorer to help researchers more easily build and export API queries; understand the data abstractions and indices available in MG-RAST; and use the results presented in-browser for exploration, development, and debugging. Conclusions: The API explorer lowers the barrier to entry for occasional or first-time MG-RAST API users.
- Open Access
- 26 September 2017
- Published by Oxford University Press (OUP) in Briefings in Bioinformatics
- Vol. 20 (4) , 1151-1159
MG-RAST version 4—lessons learned from a decade of low-budget ultra-high-throughput metagenome analysis
As technologies change, MG-RAST is adapting. Newly available software is being included to improve accuracy and performance. As a computational service constantly running large volume scientific workflows, MG-RAST is the right location to perform benchmarking and implement algorithmic or platform improvements, in many cases involving trade-offs between specificity, sensitivity and run-time cost. The work in [Glass EM, Dribinsky Y, Yilmaz P, et al. ISME J 2014;8:1–3] is an example; we use existing well-studied data sets as gold standards representing different environments and different technologies to evaluate any changes to the pipeline. Currently, we use well-understood data sets in MG-RAST as platform for benchmarking. The use of artificial data sets for pipeline performance optimization has not added value, as these data sets are not presenting the same challenges as real-world data sets. In addition, the MG-RAST team welcomes suggestions for improvements of the workflow. We are currently working on versions 4.02 and 4.1, both of which contain significant input from the community and our partners that will enable double barcoding, stronger inferences supported by longer-read technologies, and will increase throughput while maintaining sensitivity by using Diamond and SortMeRNA. On the technical platform side, the MG-RAST team intends to support the Common Workflow Language as a standard to specify bioinformatics workflows, both to facilitate development and efficient high-performance implementation of the community’s data analysis tasks.
- 26 September 2017
- Published by Oxford University Press (OUP) in Briefings in Bioinformatics
- Vol. 20 (4) , 1151-1159
Open AccessMG-RAST version 4—lessons learned from a decade of low-budget ultra-high-throughput metagenome analysis
As technologies change, MG-RAST is adapting. Newly available software is being included to improve accuracy and performance. As a computational service constantly running large volume scientific workflows, MG-RAST is the right location to perform benchmarking and implement algorithmic or platform improvements, in many cases involving trade-offs between specificity, sensitivity and run-time cost. The work in [Glass EM, Dribinsky Y, Yilmaz P, et al. ISME J 2014;8:1–3] is an example; we use existing well-studied data sets as gold standards representing different environments and different technologies to evaluate any changes to the pipeline. Currently, we use well-understood data sets in MG-RAST as platform for benchmarking. The use of artificial data sets for pipeline performance optimization has not added value, as these data sets are not presenting the same challenges as real-world data sets. In addition, the MG-RAST team welcomes suggestions for improvements of the workflow. We are currently working on versions 4.02 and 4.1, both of which contain significant input from the community and our partners that will enable double barcoding, stronger inferences supported by longer-read technologies, and will increase throughput while maintaining sensitivity by using Diamond and SortMeRNA. On the technical platform side, the MG-RAST team intends to support the Common Workflow Language as a standard to specify bioinformatics workflows, both to facilitate development and efficient high-performance implementation of the community’s data analysis tasks.
- 3 June 2016
- Published by Springer Nature
- p. 291-312
Metagenomic Design and Sequencing
- Open Access
- 9 December 2015
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 44 (D1) , D590-D594
The MG-RAST metagenomics database and portal in 2015
MG-RAST (http://metagenomics.anl.gov) is an open-submission data portal for processing, analyzing, sharing and disseminating metagenomic datasets. The system currently hosts over 200 000 datasets and is continuously updated. The volume of submissions has increased 4-fold over the past 24 months, now averaging 4 terabasepairs per month. In addition to several new features, we report changes to the analysis workflow and the technologies used to scale the pipeline up to the required throughput levels. To show possible uses for the data from MG-RAST, we present several examples integrating data and analyses from MG-RAST into popular third-party analysis tools or sequence alignment tools.
- 9 December 2015
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 44 (D1) , D590-D594
Open AccessThe MG-RAST metagenomics database and portal in 2015
MG-RAST (http://metagenomics.anl.gov) is an open-submission data portal for processing, analyzing, sharing and disseminating metagenomic datasets. The system currently hosts over 200 000 datasets and is continuously updated. The volume of submissions has increased 4-fold over the past 24 months, now averaging 4 terabasepairs per month. In addition to several new features, we report changes to the analysis workflow and the technologies used to scale the pipeline up to the required throughput levels. To show possible uses for the data from MG-RAST, we present several examples integrating data and analyses from MG-RAST into popular third-party analysis tools or sequence alignment tools.
- Open Access
- 1 July 2015
- Published by American Society for Microbiology in mBio
- Vol. 6 (3) , e00552-15-15
Eco-Evolutionary Dynamics of Episomes among Ecologically Cohesive Bacterial Populations
Although plasmids and other episomes are recognized as key players in horizontal gene transfer among microbes, their diversity and dynamics among ecologically structured host populations in the wild remain poorly understood. Here, we show that natural populations of marine Vibrionaceae bacteria host large numbers of families of episomes, consisting of plasmids and a surprisingly high fraction of plasmid-like temperate phages. Episomes are unevenly distributed among host populations, and contrary to the notion that high-density communities in biofilms act as hot spots of gene transfer, we identified a strong bias for episomes to occur in free-living as opposed to particle-attached cells. Mapping of episomal families onto host phylogeny shows that, with the exception of all phage and a few plasmid families, most are of recent evolutionary origin and appear to have spread rapidly by horizontal transfer. Such high eco-evolutionary turnover is particularly surprising for plasmids that are, based on previously suggested categorization, putatively nontransmissible, indicating that this type of plasmid is indeed frequently transferred by currently unknown mechanisms. Finally, analysis of recent gene transfer among plasmids reveals a network of extensive exchange connecting nearly all episomes. Genes functioning in plasmid transfer and maintenance are frequently exchanged, suggesting that plasmids can be rapidly transformed from one category to another. The broad distribution of episomes among distantly related hosts and the observed promiscuous recombination patterns show how episomes can offer their hosts rapid assembly and dissemination of novel functions. IMPORTANCE Plasmids and other episomes are an integral part of bacterial biology in all environments, yet their study is heavily biased toward their role as vectors for antibiotic resistance genes. This study presents a comprehensive analysis of all episomes within several coexisting bacterial populations of Vibrionaceae from the coastal ocean and represents the largest-yet genomic survey of episomes from a single bacterial family. The host population framework allows analysis of the eco-evolutionary dynamics at unprecedented resolution, yielding several unexpected results. These include (i) discovery of novel, nonintegrative temperate phages, (ii) revision of a class of episomes, previously termed “nontransmissible,” as highly transmissible, and (iii) surprisingly high evolutionary turnover of episomes, manifest as frequent birth, spread, and loss.
- 1 July 2015
- Published by American Society for Microbiology in mBio
- Vol. 6 (3) , e00552-15-15
Open AccessEco-Evolutionary Dynamics of Episomes among Ecologically Cohesive Bacterial Populations
Although plasmids and other episomes are recognized as key players in horizontal gene transfer among microbes, their diversity and dynamics among ecologically structured host populations in the wild remain poorly understood. Here, we show that natural populations of marine Vibrionaceae bacteria host large numbers of families of episomes, consisting of plasmids and a surprisingly high fraction of plasmid-like temperate phages. Episomes are unevenly distributed among host populations, and contrary to the notion that high-density communities in biofilms act as hot spots of gene transfer, we identified a strong bias for episomes to occur in free-living as opposed to particle-attached cells. Mapping of episomal families onto host phylogeny shows that, with the exception of all phage and a few plasmid families, most are of recent evolutionary origin and appear to have spread rapidly by horizontal transfer. Such high eco-evolutionary turnover is particularly surprising for plasmids that are, based on previously suggested categorization, putatively nontransmissible, indicating that this type of plasmid is indeed frequently transferred by currently unknown mechanisms. Finally, analysis of recent gene transfer among plasmids reveals a network of extensive exchange connecting nearly all episomes. Genes functioning in plasmid transfer and maintenance are frequently exchanged, suggesting that plasmids can be rapidly transformed from one category to another. The broad distribution of episomes among distantly related hosts and the observed promiscuous recombination patterns show how episomes can offer their hosts rapid assembly and dissemination of novel functions. IMPORTANCE Plasmids and other episomes are an integral part of bacterial biology in all environments, yet their study is heavily biased toward their role as vectors for antibiotic resistance genes. This study presents a comprehensive analysis of all episomes within several coexisting bacterial populations of Vibrionaceae from the coastal ocean and represents the largest-yet genomic survey of episomes from a single bacterial family. The host population framework allows analysis of the eco-evolutionary dynamics at unprecedented resolution, yielding several unexpected results. These include (i) discovery of novel, nonintegrative temperate phages, (ii) revision of a class of episomes, previously termed “nontransmissible,” as highly transmissible, and (iii) surprisingly high evolutionary turnover of episomes, manifest as frequent birth, spread, and loss.
- 21 April 2014
- Published by Wiley in Environmental Microbiology
- Vol. 16 (11) , 3443-3462
The complete genome sequence for putative H 2 ‐ and S ‐oxidizer C andidatus Sulfuricurvum sp., assembled de novo from an aquifer‐derived metagenome
Summary: We reconstructed the complete 2.4 Mb‐long genome of a previously uncultivated epsilonproteobacterium, C andidatus Sulfuricurvum sp. RIFRC ‐1, via assembly of short‐read shotgun metagenomic data using a complexity reduction approach. Genome‐based comparisons indicate the bacterium is a novel species within the S ulfuricurvum genus, which contains one cultivated representative, S . kujiense . Divergence between the species appears due in part to extensive genomic rearrangements, gene loss and chromosomal versus plasmid encoding of certain (respiratory) genes by RIFRC ‐1. Deoxyribonucleic acid for the genome was obtained from terrestrial aquifer sediment, in which RIFRC ‐1 comprised ∼ 47% of the bacterial community. Genomic evidence suggests RIFRC ‐1 is a chemolithoautotrophic diazotroph capable of deriving energy for growth by microaerobic or nitrate‐/nitric oxide‐dependent oxidation of S 0 , sulfide or sulfite or H 2 oxidation. Carbon may be fixed via the reductive tricarboxylic acid cycle. Consistent with these physiological attributes, the local aquifer was microoxic with small concentrations of available nitrate, small but elevated concentrations of reduced sulfur and NH 4 + / NH 3 ‐limited. Additionally, various mechanisms for heavy metal and metalloid tolerance and virulence point to a lifestyle well‐adapted for metal(loid)‐rich environments and a shared evolutionary past with pathogenic E psilonproteobacteria . Results expand upon recent findings highlighting the potential importance of sulfur and hydrogen metabolism in the terrestrial subsurface.
- 21 April 2014
- Published by Wiley in Environmental Microbiology
- Vol. 16 (11) , 3443-3462
The complete genome sequence for putative H 2 ‐ and S ‐oxidizer C andidatus Sulfuricurvum sp., assembled de novo from an aquifer‐derived metagenome
Summary: We reconstructed the complete 2.4 Mb‐long genome of a previously uncultivated epsilonproteobacterium, C andidatus Sulfuricurvum sp. RIFRC ‐1, via assembly of short‐read shotgun metagenomic data using a complexity reduction approach. Genome‐based comparisons indicate the bacterium is a novel species within the S ulfuricurvum genus, which contains one cultivated representative, S . kujiense . Divergence between the species appears due in part to extensive genomic rearrangements, gene loss and chromosomal versus plasmid encoding of certain (respiratory) genes by RIFRC ‐1. Deoxyribonucleic acid for the genome was obtained from terrestrial aquifer sediment, in which RIFRC ‐1 comprised ∼ 47% of the bacterial community. Genomic evidence suggests RIFRC ‐1 is a chemolithoautotrophic diazotroph capable of deriving energy for growth by microaerobic or nitrate‐/nitric oxide‐dependent oxidation of S 0 , sulfide or sulfite or H 2 oxidation. Carbon may be fixed via the reductive tricarboxylic acid cycle. Consistent with these physiological attributes, the local aquifer was microoxic with small concentrations of available nitrate, small but elevated concentrations of reduced sulfur and NH 4 + / NH 3 ‐limited. Additionally, various mechanisms for heavy metal and metalloid tolerance and virulence point to a lifestyle well‐adapted for metal(loid)‐rich environments and a shared evolutionary past with pathogenic E psilonproteobacteria . Results expand upon recent findings highlighting the potential importance of sulfur and hydrogen metabolism in the terrestrial subsurface.
- Open Access
- 8 August 2013
- Published by Springer Nature in BMC Genomics
- Vol. 14 (1) , 537
Rapid quantification of sequence repeats to resolve the size, structure and contents of bacterial genomes
Background: The numerous classes of repeats often impede the assembly of genome sequences from the short reads provided by new sequencing technologies. We demonstrate a simple and rapid means to ascertain the repeat structure and total size of a bacterial or archaeal genome without the need for assembly by directly analyzing the abundances of distinctk-mers among reads.Results: The sensitivity of this procedure to resolve variation within a bacterial species is demonstrated: genome sizes and repeat structure of five environmental strains ofE. colifrom shortIlluminareads were estimated by this method, and total genome sizes corresponded well with those obtained for the same strains by pulsed-field gel electrophoresis. In addition, this approach was applied to read-sets for completed genomes and shown to be accurate over a wide range of microbial genome sizes.Conclusions: Application of these procedures, based solely onk-mer abundances in short read data sets, allows aspects of genome structure to be resolved that are not apparent from conventional short read assemblies. This knowledge of the repetitive content of genomes provides insights into genome evolution and diversity.
- 8 August 2013
- Published by Springer Nature in BMC Genomics
- Vol. 14 (1) , 537
Open AccessRapid quantification of sequence repeats to resolve the size, structure and contents of bacterial genomes
Background: The numerous classes of repeats often impede the assembly of genome sequences from the short reads provided by new sequencing technologies. We demonstrate a simple and rapid means to ascertain the repeat structure and total size of a bacterial or archaeal genome without the need for assembly by directly analyzing the abundances of distinctk-mers among reads.Results: The sensitivity of this procedure to resolve variation within a bacterial species is demonstrated: genome sizes and repeat structure of five environmental strains ofE. colifrom shortIlluminareads were estimated by this method, and total genome sizes corresponded well with those obtained for the same strains by pulsed-field gel electrophoresis. In addition, this approach was applied to read-sets for completed genomes and shown to be accurate over a wide range of microbial genome sizes.Conclusions: Application of these procedures, based solely onk-mer abundances in short read data sets, allows aspects of genome structure to be resolved that are not apparent from conventional short read assemblies. This knowledge of the repetitive content of genomes provides insights into genome evolution and diversity.
- 1 January 2013
- Published by Elsevier
- Vol. 531, 487-523
A Metagenomics Portal for a Democratized Sequencing World
- 1 January 2013
- Published by Elsevier
- Vol. 531, 487-523
A Metagenomics Portal for a Democratized Sequencing World
- Open Access
- 28 December 2012
- Published by American Physical Society (APS) in Physical Review C
- Vol. 86 (6) , 065503
Efficient, tightly-confined trapping ofRaWe demonstrate a technique for transferring Ra atoms from a three-dimensional magneto-optical trap (MOT) into a standing wave optical dipole trap (ODT) in an adjacent chamber. The resulting small trapping volume (120 m in diameter) allows for high control of the electric and magnetic fields applied to the atoms. The atoms are first transferred to a traveling-wave optical dipole trap, which is then translated 46 cm to a science chamber. The atoms are subsequently transferred into an orthogonal standing-wave ODT by application of a one-dimensional MOT along the traveling-wave axis. For each stage, transfer efficiencies exceeding 60 are demonstrated.- 28 December 2012
- Published by American Physical Society (APS) in Physical Review C
- Vol. 86 (6) , 065503
Open AccessEfficient, tightly-confined trapping ofRaWe demonstrate a technique for transferring Ra atoms from a three-dimensional magneto-optical trap (MOT) into a standing wave optical dipole trap (ODT) in an adjacent chamber. The resulting small trapping volume (120 m in diameter) allows for high control of the electric and magnetic fields applied to the atoms. The atoms are first transferred to a traveling-wave optical dipole trap, which is then translated 46 cm to a science chamber. The atoms are subsequently transferred into an orthogonal standing-wave ODT by application of a one-dimensional MOT along the traveling-wave axis. For each stage, transfer efficiencies exceeding 60 are demonstrated. - 15 December 2012
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 194 (24) , 6986-6987
Draft Genome Sequence of Agrobacterium albertimagni Strain AOL15
Agrobacterium albertimagni strain AOL15 is an alphaproteobacterium isolated from arsenite-oxidizing biofilms whose draft genome contains 5.1 Mb in 55 contigs with 61.2% GC content and includes a 21-gene arsenic gene island. This is the first available genome for this species and the second Agrobacterium arsenic gene island.
- 15 December 2012
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 194 (24) , 6986-6987
Draft Genome Sequence of Agrobacterium albertimagni Strain AOL15
Agrobacterium albertimagni strain AOL15 is an alphaproteobacterium isolated from arsenite-oxidizing biofilms whose draft genome contains 5.1 Mb in 55 contigs with 61.2% GC content and includes a 21-gene arsenic gene island. This is the first available genome for this species and the second Agrobacterium arsenic gene island.