Show simple item record

dc.contributor.authorLynch, Joshua
dc.contributor.authorTang, Karen
dc.contributor.authorPriya, Sambhawa
dc.contributor.authorSands, Joanna
dc.contributor.authorSands, Margaret
dc.contributor.authorTang, Evan
dc.contributor.authorMukherjee, Sayan
dc.contributor.authorKnights, Dan
dc.contributor.authorBlekhman, Ran
dc.date.accessioned2018-02-12T16:43:07Z
dc.date.available2018-02-12T16:43:07Z
dc.date.issued2017-11-08
dc.identifier.citationHOMINID: a framework for identifying associations between host genetic variation and microbiome composition 2017, 6 (12):1 GigaScienceen
dc.identifier.issn2047-217X
dc.identifier.doi10.1093/gigascience/gix107
dc.identifier.urihttp://hdl.handle.net/10150/626556
dc.description.abstractRecent studies have uncovered a strong effect of host genetic variation on the composition of host-associated microbiota. Here, we present HOMINID, a computational approach based on Lasso linear regression, that given host genetic variation and microbiome taxonomic composition data, identifies host single nucleotide polymorphisms (SNPs) that are correlated with microbial taxa abundances. Using simulated data, we show that HOMINID has accuracy in identifying associated SNPs and performs better compared with existing methods. We also show that HOMINID can accurately identify the microbial taxa that are correlated with associated SNPs. Lastly, by using HOMINID on real data of human genetic variation and microbiome composition, we identified 13 human SNPs in which genetic variation is correlated with microbiome taxonomic composition across body sites. In conclusion, HOMINID is a powerful method to detect host genetic variants linked to microbiome composition and can facilitate discovery of mechanisms controlling host-microbiome interactions.
dc.description.sponsorshipUniversity of Minnesota College of Biological Sciences; Randy Shaver Cancer Research and Community Fund; American Cancer Society [124166-IRG-58-001-55-IRG53]; Alfred P. Sloan Foundationen
dc.language.isoenen
dc.publisherOXFORD UNIV PRESSen
dc.relation.urlhttp://academic.oup.com/gigascience/article/6/12/1/4602854en
dc.rights© The Author(s) 2017. Published by Oxford University Press. This is an Open Access article distributed under the terms of the Creative Commons Attribution License.en
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectmicrobiomeen
dc.subjecthost geneticsen
dc.subjectassociationen
dc.subjectmachine learningen
dc.titleHOMINID: a framework for identifying associations between host genetic variation and microbiome compositionen
dc.typeArticleen
dc.contributor.departmentUniv Arizona, Dept Agr & Biosyst Engnen
dc.identifier.journalGigaScienceen
dc.description.noteOpen Access Journal.en
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.en
dc.eprint.versionFinal published versionen
refterms.dateFOA2018-07-14T11:38:58Z
html.description.abstractRecent studies have uncovered a strong effect of host genetic variation on the composition of host-associated microbiota. Here, we present HOMINID, a computational approach based on Lasso linear regression, that given host genetic variation and microbiome taxonomic composition data, identifies host single nucleotide polymorphisms (SNPs) that are correlated with microbial taxa abundances. Using simulated data, we show that HOMINID has accuracy in identifying associated SNPs and performs better compared with existing methods. We also show that HOMINID can accurately identify the microbial taxa that are correlated with associated SNPs. Lastly, by using HOMINID on real data of human genetic variation and microbiome composition, we identified 13 human SNPs in which genetic variation is correlated with microbiome taxonomic composition across body sites. In conclusion, HOMINID is a powerful method to detect host genetic variants linked to microbiome composition and can facilitate discovery of mechanisms controlling host-microbiome interactions.


Files in this item

Thumbnail
Name:
gix107.pdf
Size:
1.746Mb
Format:
PDF
Description:
Final Published Version

This item appears in the following Collection(s)

Show simple item record

© The Author(s) 2017. Published by Oxford University Press. This is an Open Access article distributed under the terms of the Creative Commons Attribution License.
Except where otherwise noted, this item's license is described as © The Author(s) 2017. Published by Oxford University Press. This is an Open Access article distributed under the terms of the Creative Commons Attribution License.