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      DRAM for distilling microbial metabolism to automate the curation of microbiome function

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          Abstract

          Microbial and viral communities transform the chemistry of Earth's ecosystems, yet the specific reactions catalyzed by these biological engines are hard to decode due to the absence of a scalable, metabolically resolved, annotation software. Here, we present DRAM ( Distilled and Refined Annotation of Metabolism), a framework to translate the deluge of microbiome-based genomic information into a catalog of microbial traits. To demonstrate the applicability of DRAM across metabolically diverse genomes, we evaluated DRAM performance on a defined, in silico soil community and previously published human gut metagenomes. We show that DRAM accurately assigned microbial contributions to geochemical cycles and automated the partitioning of gut microbial carbohydrate metabolism at substrate levels. DRAM-v, the viral mode of DRAM, established rules to identify virally-encoded auxiliary metabolic genes (AMGs), resulting in the metabolic categorization of thousands of putative AMGs from soils and guts. Together DRAM and DRAM-v provide critical metabolic profiling capabilities that decipher mechanisms underpinning microbiome function.

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          Community structure and metabolism through reconstruction of microbial genomes from the environment.

          Microbial communities are vital in the functioning of all ecosystems; however, most microorganisms are uncultivated, and their roles in natural systems are unclear. Here, using random shotgun sequencing of DNA from a natural acidophilic biofilm, we report reconstruction of near-complete genomes of Leptospirillum group II and Ferroplasma type II, and partial recovery of three other genomes. This was possible because the biofilm was dominated by a small number of species populations and the frequency of genomic rearrangements and gene insertions or deletions was relatively low. Because each sequence read came from a different individual, we could determine that single-nucleotide polymorphisms are the predominant form of heterogeneity at the strain level. The Leptospirillum group II genome had remarkably few nucleotide polymorphisms, despite the existence of low-abundance variants. The Ferroplasma type II genome seems to be a composite from three ancestral strains that have undergone homologous recombination to form a large population of mosaic genomes. Analysis of the gene complement for each organism revealed the pathways for carbon and nitrogen fixation and energy generation, and provided insights into survival strategies in an extreme environment.
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            DFAST: a flexible prokaryotic genome annotation pipeline for faster genome publication

            Abstract Summary We developed a prokaryotic genome annotation pipeline, DFAST, that also supports genome submission to public sequence databases. DFAST was originally started as an on-line annotation server, and to date, over 7000 jobs have been processed since its first launch in 2016. Here, we present a newly implemented background annotation engine for DFAST, which is also available as a standalone command-line program. The new engine can annotate a typical-sized bacterial genome within 10 min, with rich information such as pseudogenes, translation exceptions and orthologous gene assignment between given reference genomes. In addition, the modular framework of DFAST allows users to customize the annotation workflow easily and will also facilitate extensions for new functions and incorporation of new tools in the future. Availability and implementation The software is implemented in Python 3 and runs in both Python 2.7 and 3.4—on Macintosh and Linux systems. It is freely available at https://github.com/nigyta/dfast_core/under the GPLv3 license with external binaries bundled in the software distribution. An on-line version is also available at https://dfast.nig.ac.jp/. Contact yn@nig.ac.jp Supplementary information Supplementary data are available at Bioinformatics online.
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              KofamKOALA: KEGG Ortholog assignment based on profile HMM and adaptive score threshold

              Abstract Summary KofamKOALA is a web server to assign KEGG Orthologs (KOs) to protein sequences by homology search against a database of profile hidden Markov models (KOfam) with pre-computed adaptive score thresholds. KofamKOALA is faster than existing KO assignment tools with its accuracy being comparable to the best performing tools. Function annotation by KofamKOALA helps linking genes to KEGG resources such as the KEGG pathway maps and facilitates molecular network reconstruction. Availability and implementation KofamKOALA, KofamScan and KOfam are freely available from GenomeNet (https://www.genome.jp/tools/kofamkoala/). Supplementary information Supplementary data are available at Bioinformatics online.
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                Author and article information

                Contributors
                Journal
                Nucleic Acids Res
                Nucleic Acids Res
                nar
                Nucleic Acids Research
                Oxford University Press
                0305-1048
                1362-4962
                18 September 2020
                07 August 2020
                07 August 2020
                : 48
                : 16
                : 8883-8900
                Affiliations
                Department of Soil and Crop Sciences, Colorado State University , Fort Collins, CO 80523, USA
                Department of Soil and Crop Sciences, Colorado State University , Fort Collins, CO 80523, USA
                Department of Soil and Crop Sciences, Colorado State University , Fort Collins, CO 80523, USA
                Department of Microbiology, The Ohio State University , Columbus, OH 43210, USA
                Faculty of Biosciences, Norwegian University of Life Sciences , Aas 1432, Norway
                Department of Microbiology, The Ohio State University , Columbus, OH 43210, USA
                Department of Soil and Crop Sciences, Colorado State University , Fort Collins, CO 80523, USA
                Department of Soil and Crop Sciences, Colorado State University , Fort Collins, CO 80523, USA
                Department of Soil and Crop Sciences, Colorado State University , Fort Collins, CO 80523, USA
                Department of Microbiology, The Ohio State University , Columbus, OH 43210, USA
                Department of Microbiology, The Ohio State University , Columbus, OH 43210, USA
                Department of Soil and Crop Sciences, Colorado State University , Fort Collins, CO 80523, USA
                Department of Microbiology, Radboud University , Nijmegen 6525, Netherlands
                Department of Microbiology, The Ohio State University , Columbus, OH 43210, USA
                Faculty of Biosciences, Norwegian University of Life Sciences , Aas 1432, Norway
                Department of Microbiology, The Ohio State University , Columbus, OH 43210, USA
                Joint Genome Institute, Lawrence Berkeley National Laboratory , Berkeley, CA 94720, USA
                Department of Soil and Crop Sciences, Colorado State University , Fort Collins, CO 80523, USA
                Author notes
                To whom correspondence should be addressed. Tel: +1 970 491 6517; Email: kwrighton@ 123456gmail.com

                The authors wish it to be known that, in their opinion, the first two authors should be regarded as Joint First Authors.

                Author information
                http://orcid.org/0000-0001-9023-0018
                http://orcid.org/0000-0003-3527-8101
                http://orcid.org/0000-0003-0434-4217
                Article
                gkaa621
                10.1093/nar/gkaa621
                7498326
                32766782
                22746d82-5d04-445d-b8f7-6928f6fa4e63
                © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 21 July 2020
                : 29 June 2020
                : 24 March 2020
                Page count
                Pages: 18
                Funding
                Funded by: National Science Foundation, DOI 10.13039/100000001;
                Award ID: 1759874
                Award ID: 1750189
                Award ID: 1450032
                Funded by: Wrighton Laboratory;
                Funded by: National Institutes of Health, DOI 10.13039/100000002;
                Award ID: 007447-00002
                Funded by: U.S. Department of Energy, DOI 10.13039/100000015;
                Award ID: DE-SC0018022
                Award ID: DE-AC02-05CH11231
                Categories
                AcademicSubjects/SCI00010
                Narese/24
                Computational Biology

                Genetics
                Genetics

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