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MaLiAmPi enables generalizable and taxonomy-independent microbiome features from technically diverse 16S-based microbiome studies
For studies using microbiome data, the ability to robustly combine data from technically and biologically distinct microbiome studies is a crucial means of supporting more robust and clinically relevant inferences. Formidable technical challenges arise when attempting to combine data from technicall...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10694490/ https://www.ncbi.nlm.nih.gov/pubmed/37939711 http://dx.doi.org/10.1016/j.crmeth.2023.100639 |
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author | Minot, Samuel S. Garb, Bailey Roldan, Alennie Tang, Alice S. Oskotsky, Tomiko T. Rosenthal, Christopher Hoffman, Noah G. Sirota, Marina Golob, Jonathan L. |
author_facet | Minot, Samuel S. Garb, Bailey Roldan, Alennie Tang, Alice S. Oskotsky, Tomiko T. Rosenthal, Christopher Hoffman, Noah G. Sirota, Marina Golob, Jonathan L. |
author_sort | Minot, Samuel S. |
collection | PubMed |
description | For studies using microbiome data, the ability to robustly combine data from technically and biologically distinct microbiome studies is a crucial means of supporting more robust and clinically relevant inferences. Formidable technical challenges arise when attempting to combine data from technically diverse 16S rRNA gene variable region amplicon sequencing (16S) studies. Closed operational taxonomic units and taxonomy are criticized as being heavily dependent upon reference sets and with limited precision relative to the underlying biology. Phylogenetic placement has been demonstrated to be a promising taxonomy-free manner of harmonizing microbiome data, but it has lacked a validated count-based feature suitable for use in machine learning and association studies. Here we introduce a phylogenetic-placement-based, taxonomy-independent, compositional feature of microbiota: phylotypes. Phylotypes were predictive of clinical outcomes such as obesity or pre-term birth on technically diverse independent validation sets harmonized post hoc. Thus, phylotypes enable the rigorous cross-validation of 16S-based clinical prognostic models and associative microbiome studies. |
format | Online Article Text |
id | pubmed-10694490 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-106944902023-12-05 MaLiAmPi enables generalizable and taxonomy-independent microbiome features from technically diverse 16S-based microbiome studies Minot, Samuel S. Garb, Bailey Roldan, Alennie Tang, Alice S. Oskotsky, Tomiko T. Rosenthal, Christopher Hoffman, Noah G. Sirota, Marina Golob, Jonathan L. Cell Rep Methods Article For studies using microbiome data, the ability to robustly combine data from technically and biologically distinct microbiome studies is a crucial means of supporting more robust and clinically relevant inferences. Formidable technical challenges arise when attempting to combine data from technically diverse 16S rRNA gene variable region amplicon sequencing (16S) studies. Closed operational taxonomic units and taxonomy are criticized as being heavily dependent upon reference sets and with limited precision relative to the underlying biology. Phylogenetic placement has been demonstrated to be a promising taxonomy-free manner of harmonizing microbiome data, but it has lacked a validated count-based feature suitable for use in machine learning and association studies. Here we introduce a phylogenetic-placement-based, taxonomy-independent, compositional feature of microbiota: phylotypes. Phylotypes were predictive of clinical outcomes such as obesity or pre-term birth on technically diverse independent validation sets harmonized post hoc. Thus, phylotypes enable the rigorous cross-validation of 16S-based clinical prognostic models and associative microbiome studies. Elsevier 2023-11-07 /pmc/articles/PMC10694490/ /pubmed/37939711 http://dx.doi.org/10.1016/j.crmeth.2023.100639 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Minot, Samuel S. Garb, Bailey Roldan, Alennie Tang, Alice S. Oskotsky, Tomiko T. Rosenthal, Christopher Hoffman, Noah G. Sirota, Marina Golob, Jonathan L. MaLiAmPi enables generalizable and taxonomy-independent microbiome features from technically diverse 16S-based microbiome studies |
title | MaLiAmPi enables generalizable and taxonomy-independent microbiome features from technically diverse 16S-based microbiome studies |
title_full | MaLiAmPi enables generalizable and taxonomy-independent microbiome features from technically diverse 16S-based microbiome studies |
title_fullStr | MaLiAmPi enables generalizable and taxonomy-independent microbiome features from technically diverse 16S-based microbiome studies |
title_full_unstemmed | MaLiAmPi enables generalizable and taxonomy-independent microbiome features from technically diverse 16S-based microbiome studies |
title_short | MaLiAmPi enables generalizable and taxonomy-independent microbiome features from technically diverse 16S-based microbiome studies |
title_sort | maliampi enables generalizable and taxonomy-independent microbiome features from technically diverse 16s-based microbiome studies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10694490/ https://www.ncbi.nlm.nih.gov/pubmed/37939711 http://dx.doi.org/10.1016/j.crmeth.2023.100639 |
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