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We are analyzing https://link.springer.com/article/10.1186/s40168-018-0605-2.

Title:
Simple statistical identification and removal of contaminant sequences in marker-gene and metagenomics data | Microbiome
Description:
Background The accuracy of microbial community surveys based on marker-gene and metagenomic sequencing (MGS) suffers from the presence of contaminants—DNA sequences not truly present in the sample. Contaminants come from various sources, including reagents. Appropriate laboratory practices can reduce contamination, but do not eliminate it. Here we introduce decontam ( https://github.com/benjjneb/decontam ), an open-source R package that implements a statistical classification procedure that identifies contaminants in MGS data based on two widely reproduced patterns: contaminants appear at higher frequencies in low-concentration samples and are often found in negative controls. Results Decontam classified amplicon sequence variants (ASVs) in a human oral dataset consistently with prior microscopic observations of the microbial taxa inhabiting that environment and previous reports of contaminant taxa. In metagenomics and marker-gene measurements of a dilution series, decontam substantially reduced technical variation arising from different sequencing protocols. The application of decontam to two recently published datasets corroborated and extended their conclusions that little evidence existed for an indigenous placenta microbiome and that some low-frequency taxa seemingly associated with preterm birth were contaminants. Conclusions Decontam improves the quality of metagenomic and marker-gene sequencing by identifying and removing contaminant DNA sequences. Decontam integrates easily with existing MGS workflows and allows researchers to generate more accurate profiles of microbial communities at little to no additional cost.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Science
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Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {💸}

We're unsure if the website is profiting.

Not all websites focus on profit; some are designed to educate, connect people, or share useful tools. People create websites for numerous reasons. And this could be one such example. Link.springer.com might be cashing in, but we can't detect the method they're using.

Keywords {🔍}

decontam, dna, contaminants, samples, article, contaminant, sequencing, data, frequency, google, scholar, oral, scores, prevalence, sample, methods, sequences, classification, sequence, asvs, method, contamination, negative, microbiome, score, microbial, human, mgs, analysis, controls, fig, present, dataset, cas, identification, threshold, genera, assigned, true, markergene, rrna, gene, concentration, bacterial, metagenomics, amplicon, control, extraction, seq, removal,

Topics {✒️}

apparent high-prevalence false-negative high-throughput marker-gene cross-contamination—contaminant sequences arising high-frequency cross-talk sample bray-curtis dissimilarities low-biomass carbonate rock 16s rrna gene dsdna assay kit article download pdf false-positive contaminant identification picogreen fluorescence-based quant high-resolution sample inference clearest low-score peak symbiont-rich aphid genus dual-indexed mgs libraries io/decontammanuscript/analyses/oral_contamination unambiguous reference-based classifications prevalence-based contaminant identification frequency-based contaminant identification gel-based quality control log-transformed total dna extremely low-biomass samples marker-gene data analysis identifying cross-contaminants arising full size image metagenome-assembled-genomes simple statistical identification prevalence-based score statistic privacy choices/manage cookies low-biomass contaminant database frequency-based score statistic low-frequency taxa seemingly statistical classification procedure 16s amplicon reads developed receiver-operator-characteristic operational taxonomic units amplicon sequence variants single negative control illumina amplicon data genomics-based identification human subjects research illumina miseq data marker-gene sequencing identify contaminant-specific patterns marker-gene measurements sample relative abundance marker-gene dataset microbial community surveys creative commons license include research subjects

Schema {🗺️}

WebPage:
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         headline:Simple statistical identification and removal of contaminant sequences in marker-gene and metagenomics data
         description:The accuracy of microbial community surveys based on marker-gene and metagenomic sequencing (MGS) suffers from the presence of contaminants—DNA sequences not truly present in the sample. Contaminants come from various sources, including reagents. Appropriate laboratory practices can reduce contamination, but do not eliminate it. Here we introduce decontam ( https://github.com/benjjneb/decontam ), an open-source R package that implements a statistical classification procedure that identifies contaminants in MGS data based on two widely reproduced patterns: contaminants appear at higher frequencies in low-concentration samples and are often found in negative controls. Decontam classified amplicon sequence variants (ASVs) in a human oral dataset consistently with prior microscopic observations of the microbial taxa inhabiting that environment and previous reports of contaminant taxa. In metagenomics and marker-gene measurements of a dilution series, decontam substantially reduced technical variation arising from different sequencing protocols. The application of decontam to two recently published datasets corroborated and extended their conclusions that little evidence existed for an indigenous placenta microbiome and that some low-frequency taxa seemingly associated with preterm birth were contaminants. Decontam improves the quality of metagenomic and marker-gene sequencing by identifying and removing contaminant DNA sequences. Decontam integrates easily with existing MGS workflows and allows researchers to generate more accurate profiles of microbial communities at little to no additional cost.
         datePublished:2018-12-17T00:00:00Z
         dateModified:2018-12-17T00:00:00Z
         pageStart:1
         pageEnd:14
         license:http://creativecommons.org/publicdomain/zero/1.0/
         sameAs:https://doi.org/10.1186/s40168-018-0605-2
         keywords:
            Microbiome
            Metagenomics
            Marker-gene
            16S rRNA gene
            DNA contamination
            Medical Microbiology
            Bioinformatics
            Microbial Ecology
            Microbiology
            Microbial Genetics and Genomics
            Virology
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                        name:Department of Population Health and Pathobiology, College of Veterinary Medicine, North Carolina State University, Raleigh, USA
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                     name:North Carolina State University
                     address:
                        name:Bioinformatics Research Center, North Carolina State University, Raleigh, USA
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ScholarlyArticle:
      headline:Simple statistical identification and removal of contaminant sequences in marker-gene and metagenomics data
      description:The accuracy of microbial community surveys based on marker-gene and metagenomic sequencing (MGS) suffers from the presence of contaminants—DNA sequences not truly present in the sample. Contaminants come from various sources, including reagents. Appropriate laboratory practices can reduce contamination, but do not eliminate it. Here we introduce decontam ( https://github.com/benjjneb/decontam ), an open-source R package that implements a statistical classification procedure that identifies contaminants in MGS data based on two widely reproduced patterns: contaminants appear at higher frequencies in low-concentration samples and are often found in negative controls. Decontam classified amplicon sequence variants (ASVs) in a human oral dataset consistently with prior microscopic observations of the microbial taxa inhabiting that environment and previous reports of contaminant taxa. In metagenomics and marker-gene measurements of a dilution series, decontam substantially reduced technical variation arising from different sequencing protocols. The application of decontam to two recently published datasets corroborated and extended their conclusions that little evidence existed for an indigenous placenta microbiome and that some low-frequency taxa seemingly associated with preterm birth were contaminants. Decontam improves the quality of metagenomic and marker-gene sequencing by identifying and removing contaminant DNA sequences. Decontam integrates easily with existing MGS workflows and allows researchers to generate more accurate profiles of microbial communities at little to no additional cost.
      datePublished:2018-12-17T00:00:00Z
      dateModified:2018-12-17T00:00:00Z
      pageStart:1
      pageEnd:14
      license:http://creativecommons.org/publicdomain/zero/1.0/
      sameAs:https://doi.org/10.1186/s40168-018-0605-2
      keywords:
         Microbiome
         Metagenomics
         Marker-gene
         16S rRNA gene
         DNA contamination
         Medical Microbiology
         Bioinformatics
         Microbial Ecology
         Microbiology
         Microbial Genetics and Genomics
         Virology
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                  address:
                     name:Department of Population Health and Pathobiology, College of Veterinary Medicine, North Carolina State University, Raleigh, USA
                     type:PostalAddress
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                  name:North Carolina State University
                  address:
                     name:Bioinformatics Research Center, North Carolina State University, Raleigh, USA
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         type:PostalAddress
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      address:
         name:Department of Statistics, Stanford University, Stanford, USA
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         type:PostalAddress
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      address:
         name:Department of Medicine, Stanford University School of Medicine, Stanford, USA
         type:PostalAddress
      name:Veterans Affairs Palo Alto Health Care System
      address:
         name:Infectious Diseases Section, Veterans Affairs Palo Alto Health Care System, Palo Alto, USA
         type:PostalAddress
      name:North Carolina State University
      address:
         name:Department of Population Health and Pathobiology, College of Veterinary Medicine, North Carolina State University, Raleigh, USA
         type:PostalAddress
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      address:
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      name:Nicole M. Davis
      affiliation:
            name:Stanford University School of Medicine
            address:
               name:Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, USA
               type:PostalAddress
            type:Organization
      name:Diana M. Proctor
      affiliation:
            name:Stanford University School of Medicine
            address:
               name:Department of Medicine, Stanford University School of Medicine, Stanford, USA
               type:PostalAddress
            type:Organization
            name:University of California, San Francisco School of Dentistry
            address:
               name:Department of Orofacial Sciences, University of California, San Francisco School of Dentistry, San Francisco, USA
               type:PostalAddress
            type:Organization
      name:Susan P. Holmes
      affiliation:
            name:Stanford University
            address:
               name:Department of Statistics, Stanford University, Stanford, USA
               type:PostalAddress
            type:Organization
      name:David A. Relman
      affiliation:
            name:Stanford University School of Medicine
            address:
               name:Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, USA
               type:PostalAddress
            type:Organization
            name:Stanford University School of Medicine
            address:
               name:Department of Medicine, Stanford University School of Medicine, Stanford, USA
               type:PostalAddress
            type:Organization
            name:Veterans Affairs Palo Alto Health Care System
            address:
               name:Infectious Diseases Section, Veterans Affairs Palo Alto Health Care System, Palo Alto, USA
               type:PostalAddress
            type:Organization
      name:Benjamin J. Callahan
      url:http://orcid.org/0000-0002-8752-117X
      affiliation:
            name:North Carolina State University
            address:
               name:Department of Population Health and Pathobiology, College of Veterinary Medicine, North Carolina State University, Raleigh, USA
               type:PostalAddress
            type:Organization
            name:North Carolina State University
            address:
               name:Bioinformatics Research Center, North Carolina State University, Raleigh, USA
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, USA
      name:Department of Medicine, Stanford University School of Medicine, Stanford, USA
      name:Department of Orofacial Sciences, University of California, San Francisco School of Dentistry, San Francisco, USA
      name:Department of Statistics, Stanford University, Stanford, USA
      name:Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, USA
      name:Department of Medicine, Stanford University School of Medicine, Stanford, USA
      name:Infectious Diseases Section, Veterans Affairs Palo Alto Health Care System, Palo Alto, USA
      name:Department of Population Health and Pathobiology, College of Veterinary Medicine, North Carolina State University, Raleigh, USA
      name:Bioinformatics Research Center, North Carolina State University, Raleigh, USA

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