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@ARTICLE{Eklund:154638,
author = {N. Eklund and N. H. Andrianarisoa and E. van Enckevort and
G. Anton and A. Debucquoy and H. Müller and L. Zaharenko
and C. Engels and L. Ebert$^*$ and M. Neumann and J.
Geeraert and V. T'Joen and H. Demski and É. Caboux and R.
Proynova$^*$ and B. Parodi and S. Mate and E. van Iperen and
R. Merino-Martinez and P. R. Quinlan and P. Holub and K.
Silander},
title = {{E}xtending the {M}inimum {I}nformation {A}bout {BI}obank
{D}ata {S}haring {T}erminology to {D}escribe {S}amples,
{S}ample {D}onors, and {E}vents.},
journal = {Biopreservation and biobanking},
volume = {18},
number = {3},
issn = {1947-5543},
address = {New Rochelle, NY},
publisher = {Liebert},
reportid = {DKFZ-2020-00905},
pages = {155-164},
year = {2020},
note = {2020 Jun;18(3):155-164},
abstract = {Introduction: The Minimum Information About BIobank data
Sharing (MIABIS) was initiated in 2012. MIABIS aims to
create a common biobank terminology to facilitate data
sharing in biobanks and sample collections. The MIABIS Core
terminology consists of three components describing
biobanks, sample collections, and studies, in which
information on samples and sample donors is provided at
aggregated form. However, there is also a need to describe
samples and sample donors at an individual level to allow
more elaborate queries on available biobank samples and
data. Therefore the MIABIS terminology has now been extended
with components describing samples and sample donors at an
individual level. Materials and Methods: The components were
defined according to specific scope and use cases by a large
group of experts, and through several cycles of reviews,
according to the new MIABIS governance model of BBMRI-ERIC
(Biobanking and Biomolecular Resources Research
Infrastructure-European Research Infrastructure Consortium).
The guiding principles applied in developing these
components included the following terms: model should
consider only samples of human origin, model should be
applicable to all types of samples and all sample donors,
and model should describe the current status of samples
stored in a given biobank. Results: A minimal set of
standard attributes for defining samples and sample donors
is presented here. We added an 'event' component to describe
attributes that are not directly describing samples or
sample donors but are tightly related to them. To better
utilize the generic data model, we suggest a procedure by
which interoperability can be promoted, using specific
MIABIS profiles. Discussion: The MIABIS sample and donor
component extensions and the new generic data model
complement the existing MIABIS Core 2.0 components, and
substantially increase the potential usability of this
terminology for better describing biobank samples and sample
donors. They also support the use of individual level data
about samples and sample donors to obtain accurate and
detailed biobank availability queries.},
cin = {E260},
ddc = {610},
cid = {I:(DE-He78)E260-20160331},
pnm = {315 - Imaging and radiooncology (POF3-315)},
pid = {G:(DE-HGF)POF3-315},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:32302498},
doi = {10.1089/bio.2019.0129},
url = {https://inrepo02.dkfz.de/record/154638},
}