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                "secondary-accession": "ERP021973",
                "centre-name": "UNIVERSITY OF CALGARY",
                "public-release-date": null,
                "study-abstract": "In this study we compared methods for quantifying taxonomic composition of microbial communities. The compared methods included metagenomics, 16S rRNA amplicon sequencing and metaproteomics. This ENA study contains the metagenomic and the 16S rRNA amplicon data. The metaproteomic data is available from ProteomeXchange via the PRIDE repository(PXD006118). For the comparison of the methods we analyzed three types of mock communities with all three methods. The communities contain between 28 to 32 species and strains of bacteria, archaea, eukaryotes and bacteriophage. For each community type 4 biological replicate communities were generated. All four replicates were analyzed by 16S rRNA sequencing. Three replicates of each community type were analyzed with metagenomics. The \"C\" type communities have same cell/phage particle number for all community members (C1 to C4). The \"P\" type communities have the same protein content for all community members (P1 to P4). The \"U\" (uneven) type communities cover a large range of protein amounts and cell numbers (U1 to U4). The 16S rRNA libraries were sequenced twice in independent runs. The prefixes \"rep1_\" and \"rep2_\" indicate the two individual runs. The 16S rRNA read files without prefix are rep1 and rep2 merged.",
                "study-name": "Quantification of mock microbial communities with metagenomes, 16S rRNA gene amplicons and metaproteomics",
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                "secondary-accession": "ERP127780",
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                "study-abstract": "The Third Party Annotation (TPA) assembly was derived from the primary whole genome shotgun (WGS) data set PRJEB19901, and was assembled with metaSPAdes v3.14.1. This project includes samples from the following biomes: root:Engineered:Modeled:Simulated communities (microbial mixture).",
                "study-name": "EMG produced TPA metagenomics assembly of PRJEB19901 data set (Quantification of mock microbial communities with metagenomes, 16S rRNA gene amplicons and metaproteomics).",
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            "type": "studies",
            "id": "MGYS00005461",
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                "accession": "MGYS00005461",
                "bioproject": "PRJEB31430",
                "samples-count": 8,
                "is-private": false,
                "last-update": "2020-05-22T08:52:58",
                "secondary-accession": "ERP113991",
                "centre-name": "EMG",
                "public-release-date": null,
                "study-abstract": "The Third Party Annotation (TPA) assembly was derived from the primary whole genome shotgun (WGS) data set: PRJEB6941.  This project includes samples from the following biomes: root:Engineered:Modeled:Simulated communities (microbial mixture).",
                "study-name": "EMG produced TPA metagenomics assembly of the PRJEB6941 data set (Evaluation of methods to purify virus-like particles for the sequencing of intestinal viromes).",
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                "accession": "MGYS00005462",
                "bioproject": "PRJEB6941",
                "samples-count": 7,
                "is-private": false,
                "last-update": "2020-05-22T03:34:08",
                "secondary-accession": "ERP006614",
                "centre-name": "UT SOUTHWESTERN MEDICAL CENTER",
                "public-release-date": null,
                "study-abstract": "In this study we used an in vitro assembled microbiota sample to evaluate the efficiency and biases of purification methods used to purify virus-like particles from gut content for metagenome sequencing. The artificial microbiome sample contained six bacteriophages (P22, phiVPE25, phi6, T3, T7 and M13)two bacterial strains (gr+: Listeria monocytogenes EGD-e and gr-: Bacteroides thetaiotaomicron VPI5482), which were mixed into feces from germ-free mice.  Three purification methods were tested: (1) Filtration + DNase (FD), (2) DTT treatment + filtration + DNase (DTT), (3) filtration + DNase + CsCl density gradient (CsCl). Additionally, metagenomes of the complete microbiome sample were sequenced (MG). Each treatment was done in duplicate.",
                "study-name": "Evaluation of methods to purify virus-like particles for the sequencing of intestinal viromes",
                "data-origination": "SUBMITTED"
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            "id": "MGYS00002999",
            "attributes": {
                "accession": "MGYS00002999",
                "bioproject": "PRJNA182065",
                "samples-count": 22,
                "is-private": false,
                "last-update": "2019-11-07T16:14:20",
                "secondary-accession": "SRP017282",
                "centre-name": "IOCAS",
                "public-release-date": null,
                "study-abstract": "Study the bacterial community structure and discuss the environmental relatedness.  Collected from seawater and sediment from the ECS.",
                "study-name": "Synthetic marine metagenome high-throughput sequencing",
                "data-origination": "HARVESTED"
            },
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        },
        {
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            "id": "MGYS00001765",
            "attributes": {
                "accession": "MGYS00001765",
                "bioproject": "PRJNA318988",
                "samples-count": 10,
                "is-private": false,
                "last-update": "2019-11-07T16:14:18",
                "secondary-accession": "SRP073604",
                "centre-name": "Uppsala University",
                "public-release-date": null,
                "study-abstract": "Sequencing a mock community consisting of T. roseus DSM 18391, C. akajimensis DSM 45221, P. stutzeri DSM 4166, P. inhibens DSM17395, and G. obscurus DSM 43160 for a comparative analysis of multiple displacement amplification performed in standard bulk reactions or in emulsions. Samples also include unamplified controls and no template negative controls.",
                "study-name": "5 bacterial species mock community genome sequencing",
                "data-origination": "HARVESTED"
            },
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            "id": "MGYS00001675",
            "attributes": {
                "accession": "MGYS00001675",
                "bioproject": "PRJNA267701",
                "samples-count": 240,
                "is-private": false,
                "last-update": "2019-11-07T16:14:16",
                "secondary-accession": "SRP050185",
                "centre-name": "Virginia Commonwealth University",
                "public-release-date": null,
                "study-abstract": "The goals of this project are to quantify and characterize bias in 16S rRNA Studies due to a particular choice of DNA extraction, PCR amplification, and sequencing and taxonomic classification protocols. Labs will make choices in protocol based on the environment of interest, but bias will always remain. This experiment is designed to quantify the differences between actual and observed community compositions when equal numbers of 1) cells, 2) DNA, and 3) PCR product are blended. By comparing the results of the experiments, one can quantify the contribution to bias of each step. Also, one can build models to predict true community composition based on the observed community composition.",
                "study-name": "Quantifying Bias in 16S rRNA Experiments due to DNA Extraction, PCR Amplification, and Sequencing and Classification",
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            "id": "MGYS00003675",
            "attributes": {
                "accession": "MGYS00003675",
                "bioproject": "PRJEB30057",
                "samples-count": 12,
                "is-private": false,
                "last-update": "2018-12-14T11:07:50",
                "secondary-accession": "ERP112442",
                "centre-name": "UNIVERSITY OF LAUSANNE",
                "public-release-date": null,
                "study-abstract": "To study which genes are specifically induced during the different growth phases in toluene, which could indicate the changes in BTEX metabolism as well as the biological processes affected during the different growth phases, a controlled RNA-seq transcriptome analysis was carried out. Gene expression levels were analyzed from cultures upon inoculation (T0), after 4(T4) and 24(T24) hours after inoculation in minimal medium with toluene.",
                "study-name": "Growth phase-associated changes in the transcriptome of Pseudomonas veronii 1YdBTEX2 in minimal media with toluene.",
                "data-origination": "SUBMITTED"
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        },
        {
            "type": "studies",
            "id": "MGYS00003509",
            "attributes": {
                "accession": "MGYS00003509",
                "bioproject": "PRJEB24936",
                "samples-count": 280,
                "is-private": false,
                "last-update": "2018-11-26T14:55:22",
                "secondary-accession": "ERP106804",
                "centre-name": "INRA-UM2",
                "public-release-date": null,
                "study-abstract": "Entomopathogenic nematodes from the genus Steinernema are used in biological control of insect pests. The free form of the nematode (infective juvenile) is in closed symbiotic association with the intestinal bacteria Xenorhabdus (Enterobacteriaceae). In the well-studied Steinernema carpocapsae - Xenorhabdus nematophila couple, it was largely shown that the bacterial symbiont played an important role in the death of the insect and in the elimination of the microbial competitors inside the insect cadaver. However, in addition to symbiotic bacteria, other cultivable bacteria have been regularly isolated from infective juveniles nematodes.In this study,we used both culture-dependent and multigenic metabarcoding methods to obtain a comprehensive survey of S. carpocapsae bacterial microbiota. We used two markers, the V3-V4 region of the 16S rRNA gene and a region of the rpoB gene, for which a database was built. We identified a core-microbiota of about 10 OTUs that were present in more than 70% of the samples. Representative bacterial strains of the core-microbiota were tested for their insecticidal performances and their ability to produce antimicrobial molecules.",
                "study-name": "Description of the bacterial microbiota of EntomoPathogenic Nematodes (EPNs)of Steinernema genus",
                "data-origination": "SUBMITTED"
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