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dc.contributor.authorBarber, DG
dc.contributor.authorDavies, CA
dc.contributor.authorHartley, IP
dc.contributor.authorTennant, RK
dc.date.accessioned2024-10-01T15:21:52Z
dc.date.issued2024-09-19
dc.date.updated2024-10-01T14:21:20Z
dc.description.abstractMetatranscriptomic analysis of the soil microbiome has the potential to reveal molecular mechanisms that drive soil processes regulated by the microbial community. Therefore, RNA samples must be of sufficient yield and quality to robustly quantify differential gene expression. While short-read sequencing technology is often favoured for metatranscriptomics, long-read sequencing has the potential to provide several benefits over short-read technologies. The ability to resolve complete transcripts on a portable sequencing platform for a relatively low capital expenditure makes Oxford Nanopore Technology an attractive prospect for addressing many of the challenges of soil metatranscriptomics. To fully enable long-read metatranscriptomic analysis of the functional molecular pathways expressed in these diverse habitats, RNA purification methods from soil must be optimised for long-read sequencing. Here we compare RNA samples purified using five commercially available extraction kits designed for use with soil. We found that the Qiagen RNeasy PowerSoil Total RNA Kit performed the best across RNA yield, quality and purity and was robust across different soil types. We found that sufficient sequencing depth can be achieved to characterise the active community for total RNA samples using Oxford Nanopore Technology, and discuss its current limitations for differential gene expression analysis in soil studies.en_GB
dc.description.sponsorshipShell Research Ltd.en_GB
dc.identifier.citationVol. 10(9), article 001298en_GB
dc.identifier.doihttps://doi.org/10.1099/mgen.0.001298
dc.identifier.grantnumberCW648947-PT34767en_GB
dc.identifier.urihttp://hdl.handle.net/10871/137584
dc.identifierORCID: 0000-0003-3033-1858 (Tennant, Richard K)
dc.language.isoenen_GB
dc.publisherMicrobiology Societyen_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/39298196en_GB
dc.rights© 2024 The Authors. This is an open-access article distributed under the terms of the Creative Commons Attribution License.en_GB
dc.subjectOxford Nanoporeen_GB
dc.subjectRNAen_GB
dc.subjectmetatranscriptomicsen_GB
dc.subjectsoilen_GB
dc.subjectkit comparisonen_GB
dc.subjectmicrobiomeen_GB
dc.titleEvaluation of commercial RNA extraction kits for long-read metatranscriptomics in soilen_GB
dc.typeArticleen_GB
dc.date.available2024-10-01T15:21:52Z
dc.identifier.issn2057-5858
exeter.place-of-publicationEngland
dc.descriptionThis is the final version. Available on open access from the Microbiology Society via the DOI in this recorden_GB
dc.descriptionData Summary: The datasets generated during the current study are available in the NCBI Sequence Read Archive repository, PRJNA1079547en_GB
dc.identifier.eissn2057-5858
dc.identifier.journalMicrobial Genomicsen_GB
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2024-09-03
dcterms.dateSubmitted2024-04-02
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2024-09-19
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2024-10-01T15:20:17Z
refterms.versionFCDVoR
refterms.dateFOA2024-10-01T15:22:01Z
refterms.panelCen_GB
refterms.dateFirstOnline2024-09-19
exeter.rights-retention-statementNo


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© 2024 The Authors. This is an open-access article distributed under the terms of the Creative Commons Attribution License.
Except where otherwise noted, this item's licence is described as © 2024 The Authors. This is an open-access article distributed under the terms of the Creative Commons Attribution License.