Single-cell RNA sequencing of intramedullary canal tissue to improve methods for studying fracture repair biology

dc.contributor.authorDominguez, James M., II
dc.contributor.authorMoe, Sharon M.
dc.contributor.authorChen, Neal X.
dc.contributor.authorMcKinley, Todd O.
dc.contributor.authorBrown, Krista M.
dc.contributor.authorLiu, Yunlong
dc.contributor.authorGao, Hongyu
dc.contributor.authorNatoli, Roman M.
dc.contributor.departmentMedicine, School of Medicineen_US
dc.date.accessioned2023-02-08T19:08:21Z
dc.date.available2023-02-08T19:08:21Z
dc.date.issued2021-08
dc.description.abstractThe ability to study the bone microenvironment of failed fracture healing may lead to biomarkers for fracture nonunion. Herein the authors describe a technique for isolating individual cells suitable for single-cell RNA sequencing analyses from intramedullary canal tissue collected by reaming during surgery. The purpose was to detail challenges and solutions inherent to the collection and processing of intramedullary canal tissue samples. The authors then examined single-cell RNA sequencing data from fresh and reanimated samples to demonstrate the feasibility of this approach for prospective studies.en_US
dc.eprint.versionFinal published versionen_US
dc.identifier.citationDominguez, J. M., Moe, S. M., Chen, N. X., McKinley, T. O., Brown, K. M., Liu, Y., Gao, H., & Natoli, R. M. (2021). Single-cell RNA sequencing of intramedullary canal tissue to improve methods for studying fracture repair biology. BioTechniques, 71(2), 431–438. https://doi.org/10.2144/btn-2021-0002en_US
dc.identifier.urihttps://hdl.handle.net/1805/31180
dc.language.isoenen_US
dc.publisherFuture Scienceen_US
dc.relation.isversionof10.2144/btn-2021-0002en_US
dc.relation.journalBioTechniquesen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourcePublisheren_US
dc.subjectcell isolationen_US
dc.subjectcryopreservationen_US
dc.subjectfractureen_US
dc.titleSingle-cell RNA sequencing of intramedullary canal tissue to improve methods for studying fracture repair biologyen_US
dc.typeArticleen_US
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