Show simple item record

dc.contributor.authorNanda, Sumit
dc.contributor.authorChen, Hanbo
dc.contributor.authorDas, Ravi
dc.contributor.authorBhattacharjee, Shatabdi
dc.contributor.authorCuntz, Hermann
dc.contributor.authorTorben-Nielsen, Benjamin
dc.contributor.authorPeng, Hanchuan
dc.contributor.authorCox, Daniel N.
dc.contributor.authorSchutter, Erik De
dc.contributor.authorAscoli, Giorgio A.
dc.date.accessioned2018-06-07T16:14:59Z
dc.date.available2018-06-07T16:14:59Z
dc.date.issued2018-01-23
dc.identifier.citationNanda , S , Chen , H , Das , R , Bhattacharjee , S , Cuntz , H , Torben-Nielsen , B , Peng , H , Cox , D N , Schutter , E D & Ascoli , G A 2018 , ' Design and implementation of multi-signal and time-varying neural reconstructions ' , Scientific Data , vol. 5 , 170207 . https://doi.org/10.1038/sdata.2017.207
dc.identifier.otherPURE: 13379239
dc.identifier.otherPURE UUID: af9e9cf0-9aeb-4f71-ab0b-e4f52f752752
dc.identifier.otherScopus: 85040984305
dc.identifier.urihttp://hdl.handle.net/2299/20164
dc.descriptionOpen Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
dc.description.abstractSeveral efficient procedures exist to digitally trace neuronal structure from light microscopy, and mature community resources have emerged to store, share, and analyze these datasets. In contrast, the quantification of intracellular distributions and morphological dynamics is not yet standardized. Current widespread descriptions of neuron morphology are static and inadequate for subcellular characterizations. We introduce a new file format to represent multichannel information as well as an open-source Vaa3D plugin to acquire this type of data. Next we define a novel data structure to capture morphological dynamics, and demonstrate its application to different time-lapse experiments. Importantly, we designed both innovations as judicious extensions of the classic SWC format, thus ensuring full back-compatibility with popular visualization and modeling tools. We then deploy the combined multichannel/time-varying reconstruction system on developing neurons in live Drosophila larvae by digitally tracing fluorescently labeled cytoskeletal components along with overall dendritic morphology as they changed over time. This same design is also suitable for quantifying dendritic calcium dynamics and tracking arbor-wide movement of any subcellular substrate of interest.en
dc.language.isoeng
dc.relation.ispartofScientific Data
dc.subjectStatistics and Probability
dc.subjectInformation Systems
dc.subjectEducation
dc.subjectComputer Science Applications
dc.subjectStatistics, Probability and Uncertainty
dc.subjectLibrary and Information Sciences
dc.titleDesign and implementation of multi-signal and time-varying neural reconstructionsen
dc.contributor.institutionUniversity of Hertfordshire
dc.description.statusPeer reviewed
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=85040984305&partnerID=8YFLogxK
rioxxterms.versionVoR
rioxxterms.versionofrecordhttps://doi.org/10.1038/sdata.2017.207
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record