scholarly journals Robust Integration of Biodiversity Data by Process- and State-based Representation of Object Histories and Modular Application Architecture

Author(s):  
Christian Bölling ◽  
Satpal Bilkhu ◽  
Christian Gendreau ◽  
Falko Glöckler ◽  
James Macklin ◽  
...  

Biodiversity data is obtained by a variety of methodological approaches—including observation surveys, environmental sampling and biological object collection—employing diverse sample processing protocols and data transformations. While complete and accurate accounts of these data-generating processes are important to enable integration and informed reuse of data, the structure and content of published biodiversity data currently are often shaped by specific application goals. For example, data publishers that export specimen-based data from collection management systems for inclusion in aggregations like those in the Global Biodiversity Information Facility (GBIF) must frequently relax their internal models and produce unnatural joins to fit GBIF’s occurrences-based data structure. Third-party assertions over these aggregated data therefore assume the risk of irreproducibility or concept drift. Here we introduce process- and state-based representation of object histories as the main organizing principle for data about specimens and samples in Digital Information System for Natural History Data (DINA, Glöckler et al. 2020)-compliant collection management software (Fig. 1). Specimens, samples and objects in general are subjected to a variety of processes, including planned actions involving the object, e.g., collecting, preparing, subsampling, loaning. Object states are any particular mode of being of an object at a certain point in time. For example, any one intermediate step in preparing a collected specimen for long-term conservation in a collection would constitute an individual object state. An object’s history is the entire chain of these interrelated processes and states. We argue that using object histories as main conceptual modeling paradigm in DINA offers the generality required to accommodate a diverse, open set of use cases in biodiversity data representation, yet also offers the versatility to serve as basis for use-case specific data aggregation and presentation. Specifically, a representation based on object histories provides a coherent structure for documenting individual processes and states for any given object and for linking this documentation (e.g., textual descriptions or images pertaining to a given process or state), a natural representational structure of the real-world sequence of processes an object participates in and for the data generated in these processes (e.g., a DNA-extraction procedure and sequence information generated on its basis), a straightforward structure to link data about related objects (e.g., tissue samples, the biological specimen a bone is derived from) in a network of connected object histories. a coherent structure for documenting individual processes and states for any given object and for linking this documentation (e.g., textual descriptions or images pertaining to a given process or state), a natural representational structure of the real-world sequence of processes an object participates in and for the data generated in these processes (e.g., a DNA-extraction procedure and sequence information generated on its basis), a straightforward structure to link data about related objects (e.g., tissue samples, the biological specimen a bone is derived from) in a network of connected object histories. The approach is designed to be embedded in DINA’s modular application architecture, so that information on object histories can be accessed via corresponding APIs either through its own interfaces (Fig. 2) or by integration with external web services (Fig. 3). Viewing collection management tasks as part of object histories also informs delineation of modules to support these tasks with specialized functions and interfaces. It also admits the use of persistent, dereferencable identifiers for individual processes and states in object histories and for linking their representations to elements in ontologies and controlled vocabularies. In this contribution to the symposium, DINA's object histories as a main organizing principle for collection object data will be discussed and the utility of using it in the context of modular application architecture, data federation, and data integration in projects like BiCIKL will be illustrated.

2021 ◽  
Vol 39 (15_suppl) ◽  
pp. e16532-e16532
Author(s):  
Ralph M. Wirtz ◽  
Richard Watts ◽  
Ronny Kellner ◽  
Reinhard Ortmann ◽  
Torsten Horns ◽  
...  

e16532 Background: The objective of the present study was to assess FGFR mutattions and fusions from matched urine and tissue samples from patients suspicious of bladder cancer and undergoing first TURB at the pilot center of the multicentric BRIDGister RealWorld Experience trial Methods: For this pilot study paraffin fixed pretreatment tissue samples from the first TURB of 28 pts participating in the BRIDGister trial and matched urine samples were prospectively collected and analyzed. RNA from FFPE tissues were extracted by commercial kits and analyzed by Therascreen FGFR IVD kit (Qiagen GmbH, Hilden). In addition urine samples were shipped for central isolation of extracellular vesicles and extraction of RNA (exoRNA.Exosome Diagnostics GmbH, Martinsried) and subsequently centrally analyzed by QIAcuity digital PCR (Qiagen, Hilden). Additional urine testing was performed by further technologies including central cytology. Concordance, Kruskal-Wallis, MannWhitney and Sensitivity/Specificity tests were analyzed by JMP 9.0.0 (SAS software). Results: The pilot cohort of the BRIDGister trial consisted of 28 patients (median age: 73, male 71% vs female 29%) of diverse clinical stages (Benign lesions/no tumor 21%, pTa 32%, pT1 21%, pT2 21%) and WHO 1973 grade (G1 7%, G2 43%, G3 21%). Based on FFPE tissue testing using Therascreen FGFR IVD kit 9 out of 28 patients exhibited FGFR alterations (32%). Based on exosomal RNA (exoRNA) and subsequent dPCR testing 8 out of 21 matched urine sampels were FGFR positive (38%). Comparison with tissue testing as probable gold standard revealed 71% sensitivity, 78% specificity, 63% PPV and 85%NPV. There were 3 patients being FGFR positive for exoRNA from urine with no mutation found in the corresponding TUR biopsy. One of these mutations could be validated by independent urine test. Furthermore one tumor harbored two tissue mutations (R248C, Y373C) but three urine mutations (R248C, Y373C, G370C) indicating substantial tumor heterogeneity. One FGFR3-TACC3 fusion was detected from a benign lesion, which was not found by the exosomal urine test. Conclusions: Extraction of exosomal RNA from urine followed by highly sensitive dPCR mutation testing is feasible with good concordance to matched tissue testing. Urine testing bears the potential of detecting additional mutations in a real world setting and might evolve as alternative approach for FGFR3 screening in a non invasive fashion without the need of transurethral biopsy. Discordant cases are further followed up and might reveal validation of mutation status in upcoming recurrences.Further exploration is warranted and includes the potential of monitoring patients with FGFR before and after therapeutic intervention. By the time of the congress an update of the data with approximately 50 matched pairs will be presented.


2018 ◽  
Vol 2 ◽  
pp. e26083
Author(s):  
Teresa Mayfield

At an institution without a permanent collections manager or curators, who has time to publish data or research issues on that data? Collections with little or no institutional support often benefit from passionate volunteers who continually seek ways to keep them relevant. The University of Texas at El Paso Biodiversity Collections (UTEP-BC) has been cared for in this manner by a small group of dedicated faculty and emeritus curators who have managed with no budget to care for the specimens, perform and publish research about them, and publish a good portion of the collections data. An IMLS grant allowed these dedicated volunteers to hire a Collections Manager who would migrate the already published data from the collections and add unpublished specimen records from the in-house developed FileMaker Pro database to a new collection management system (Arctos) that would allow for better records management and ease of publication. Arctos is a publicly searchable web-based system, but most collections also see the benefit of participation with biodiversity data aggregators such as the Global Biodiversity Information Facility (GBIF), iDigBio, and a multitude of discipline-specific aggregators. Publication of biodiversity data to aggregators is loaded with hidden pathways, acronyms, and tech-speak with which a curator, registrar, or collections manager may not be familiar. After navigating the process to publish the data the reward is feedback! Now data can be improved, and everyone wins, right? In the case of UTEP-BC data, the feedback sits idle as the requirements of the grant under which the Collection Manager was hired take precedence. It will likely remain buried until long after the grant has run its course. Fortunately, the selection of Arctos as a collection management system allowed the UTEP-BC Collection Manager to confer with others publishing biodiversity data to the data aggregators. Members of the Arctos Community have carried on multiple conversations about publishing to aggregators and how to handle the resulting data quality flags. These conversations provide a synthesis of the challenges experienced by collections in over 20 institutions when publishing biodiversity data to aggregators and responding (or not) to their data quality flags. This presentation will cover the experiences and concerns of one Collection Manager as well as those of the Arctos Community related to publishing data to aggregators, deciphering their data quality flags, and development of appropriate responses to those flags.


2011 ◽  
Vol 19 (1-2) ◽  
pp. 23-27 ◽  
Author(s):  
Dragan Milicevic ◽  
Milijan Jovanovic ◽  
Vesna Matekalo-Sverak ◽  
Tatjana Radicevic ◽  
Milan Petrovic ◽  
...  

Background: Toxicological investigations of tissues of normally slaughtered chickens were carried out to provide preliminary evaluation of the incidence of OTA in chicken tissues (n=90). Majority of tissue samples were not found to contain measurable amounts of OTA, while in general, the OTA levels found in the analyzed tissue were low. Methods: The presence of OTA in tissue samples was determined by HPLC-FL after liquid-liquid extraction procedure. Method validation was performed according to the Commission Decision 2002/657/EC. Results: Of the 90 liver, kidney and gizzard samples originating from chicken farms located in the different agricultural areas of Serbia, OTA was reported in 23 (38.33%), 17 (28.3%) and 16 (26.6%) samples, respectively, with levels ranging from 0.14 to 3.9 ng/g in liver, 0.1 to 7.02 ng/g in kidneys and 0.25 to 9.94 ng/g in gizzard. None of the tissue samples contained more than the maximum level (10 ng/g) recommended by the European Commission. Conclusion: Low OTA results also suggested that chicken meat available in the retail market is unlikely to pose an adverse health risk to the consumers in respect to OTA toxicity.


2019 ◽  
Vol 221 (Supplement_4) ◽  
pp. S383-S388
Author(s):  
Claude Kwe Yinda ◽  
Stephanie N Seifert ◽  
Philip Macmenamin ◽  
Neeltje van Doremalen ◽  
Lewis Kim ◽  
...  

Abstract Viruses in the genus Henipavirus encompass 2 highly pathogenic emerging zoonotic pathogens, Hendra virus (HeV) and Nipah virus (NiV). Despite the impact on human health, there is currently limited full-genome sequence information available for henipaviruses. This lack of full-length genomes hampers our ability to understand the molecular drivers of henipavirus emergence. Furthermore, rapidly deployable viral genome sequencing can be an integral part of outbreak response and epidemiological investigations to study transmission chains. In this study, we describe the development of a reverse-transcription, long-range polymerase chain reaction (LRPCR) assay for efficient genome amplification of NiV, HeV, and a related non-pathogenic henipavirus, Cedar virus (CedPV). We then demonstrated the utility of our method by amplifying partial viral genomes from 6 HeV-infected tissue samples from Syrian hamsters and 4 tissue samples from a NiV-infected African green monkey with viral loads as low as 52 genome copies/mg. We subsequently sequenced the amplified genomes on the portable Oxford Nanopore MinION platform and analyzed the data using a newly developed field-deployable bioinformatic pipeline. Our LRPCR assay allows amplification and sequencing of 2 or 4 amplicons in semi-nested reactions. Coupled with an easy-to-use bioinformatics pipeline, this method is particularly useful in the field during outbreaks in resource-poor environments.


2021 ◽  
pp. 146906672110027
Author(s):  
Shovkatjon Akhunov ◽  
Khatam Ashurov ◽  
Sherzod Axmedov ◽  
Beknazar Kasimov ◽  
Vladimir Rotshteyn ◽  
...  

This paper demonstrates direct detection of stimulants such as amphetamine, methamphetamine and cocaine spiked with untreated urine and a real world sample using surface ionization mass spectrometry. Spiked samples were analyzed without preliminary chromatographic separation and extraction procedure using the developed method. Moreover, in order to check the analytical capabilities of the method non-extracted real world sample was analyzed. After liquid–liquid extraction, the same sample was analyzed using the method for comparative study. Limit of detection of spiked samples was in the range of 10 pg (10 ng/ml) to 100 pg (100 ng/ml). Linear ranges of samples were two orders of magnitude or more than two orders of magnitude. It was revealed these spiked samples and real world sample can be analyzed without preliminary chromatographic separation and preliminary extraction procedure due to high selectivity of the method and the presence of the indicator lines of studied analytes in the mass spectra. The surface ionization mass spectrometry data was attested by the GC/MS analysis of these samples.


2021 ◽  
Vol 5 ◽  
Author(s):  
Damian M. Menning ◽  
Hunter A. Gravley ◽  
Melissa N. Cady ◽  
Daniel Pepin ◽  
Sandy Wyllie-Echeverria ◽  
...  

Seagrass meadows provide important ecological services to the marine environment but are declining worldwide. Although eelgrass meadows in the north Pacific are thought to be relatively healthy, few studies have assessed the presence of known disease pathogens in these meadows. In a pilot study to test the efficacy of the methods and to provide foundational disease biodiversity data in the north Pacific, we leveraged metabarcoding of environmental DNA extracted from water, sediment, and eelgrass tissue samples collected from five widely distributed eelgrass meadows in Alaska and one in Japan and uncovered wide prevalence of two classes of pathogenic organisms – Labyrinthula zosterae and other associated strains of Labyrinthula, and the Phytophthora/Halophytophthora blight species complex – known to have caused decline in eelgrass (Zostera marina) elsewhere in the species’ global distribution. Although the distribution of these disease organisms is not well understood in the north Pacific, we uncovered the presence of at least one eelgrass pathogen at every locality sampled.


2015 ◽  
Vol 24 (1) ◽  
pp. 1-16
Author(s):  
MTA Chowdhury ◽  
L Nesa ◽  
SM Imamul Huq

The phytoavailability of copper (Cu) and nickel (Ni) in soils from Bangladesh was assessed. The uptake by Ipomoea aquatica and Oryza sativa L. was measured and a range of extractants tested on soils and plant tissue samples. Extractants tested were distilled water, 1 M NH4Cl, 0.01 M CaCl2, 0.005 M diethylenetriamine penta‐acetic acid (DTPA), 0.1 M ethylenediamine tetraacetic acid (EDTA), 0.1 M HCl and 1 M HCl. The extractability of the metals varied depending on the metal species, the crop and the extractant used. The best extractant was 1 M HCl, which extracted the highest amount of the heavy metals and correlated most strongly with their plant uptake measures. The use of 1 M HCl is, therefore, recommended for first‐level screening of soils contaminated with heavy metals if only one extractant is to be used. Sequential extraction showed that Cu was associated mostly with the 0.005 M DTPA and 0.1 M EDTA extractable fractions, while Ni was associated with the 0.1 M HCl and 1 M HCl fractions in most cases. The fractions of metals extracted using the sequential extraction procedure varied compared to single extractions for all soil types. Dhaka Univ. J. Biol. Sci. 24(1): 1-16, 2015 (January)


2021 ◽  
Vol 39 (15_suppl) ◽  
pp. e16533-e16533
Author(s):  
Ralph M. Wirtz ◽  
Frank Friedersdorff ◽  
Elke Veltrup ◽  
Ergin Kilic ◽  
Richard Watts ◽  
...  

e16533 Background: The objective of the present study was to identify molecular charactersitics associated with FGFR positive tumors in matched urine and TUR biopsy samples from patients being suspicious of bladder cancer and undergoing first TURB at the pilot center of the multicentric BRIDGister Real World Experience trial that are helpful for patient management and prognosis. Methods: For this pilot study paraffin fixed pretreatment tissue samples from the first TURB of 28 pts participating in the BRIDGister trial and matched urine samples were prospectively collected and analyzed. RNA from FFPE tissues were extracted by commercial kits and analyzed by Therascreen FGFR IVD kit (Qiagen GmbH, Hilden). Relative gene expression of subtyping markers (KRT5, KRT0) as well as FGFR1, FGFR2, FGFR3, FGFR4, ERBB2 was centrally tested by standardized test systems (STRATIFYER Molecular Pathology GmbH, Cologne). In addition urine samples were analyzed by commercially available urine tests (UBC Rapid, BTA stat, NMP22). Spearman correlation, Kruskal-Wallis, MannWhitney and Sensitivity/Specificity tests were done by JMP 9.0.0 (SAS software). Results: The pilot cohort of the BRIDGister trial consisted of 28 patients (median age: 73, male 71% vs female 29%) of diverse clinical stages (Benign lesions/no tumor 21%, pTa 32%, pT1 21%, pT2 21%) and WHO 1973 grade (G1 7%, G2 43%, G3 21%). Based on FFPE tissue testing using Therascreen FGFR IVD kit 9 out of 28 patients exhibited FGFR alterations (32%). FGFR positive tumors were associated with high expression of FGFR3 mRNA (r = 5.951, p = 0.0011) but low FGFR1 mRNA as well as FGFR4 mRNA (r = -0.3882, p = 0.0412 and r = -0.6305, p = 0.0004, respectively). Interestingly, FGFR alteration was positively associated with the basal marker KRT5 (r = 0.3929, p = 0.0386), but not with luminal KRT20 mRNA expression (r = -0.0208, p = 0.9179). Moreover FGFR3 altered bladder cancer was associated with elevated NMP22 levels in pretreatment urine (r = 0.3978, p = 0.0361). Conclusions: In early bladder cancer FGFR3 alterations are tightly associated with a characteristic FGFR mRNA signature. Mutation/Fusion of FGFR3 results in high FGFR3 but low FGFR1 and FGFR4 mRNA expression, which might be i.a. relevant for the response to FGFR inhibition and important to predict outcome of FGFR inhibitors. Morever FGFR alteration was associated with elevated NMP22 urine levels, which might be helpful for detecting and monitoring FGFR altered bladder cancer in a non invasive fashion. These results warrant further investigation and its impact on outcome prediction (BCG responsiveness, recurrence, proegression, etc) will be prospectively analyzed in the framework of the ongoing multicenter BRIDGister Real World Experience trial.


2020 ◽  
Vol 143 ◽  
pp. 02014
Author(s):  
Yixian Shao ◽  
Bangting Xie ◽  
Mengqi Li ◽  
Xiang Zhang ◽  
Hua Xiao

Soils, as well as paddy tissue samples, were collected in the Se-rich area of Jinhua County, Zhejiang Province, China. Sequential extraction procedure was used for selenium (Se) fractionation, including soluble Se, exchangeable Se, carbonate-bound Se, iron and manganese oxide-bound Se, humic acids-bound Se, organic matter-bound Se, and the residual Se fraction. The results showed that soluble Se, exchangeable Se, carbonate-bound Se, iron and manganese oxide-bound Se fractions accounted for less than 2% of the total Se, respectively. Organic matter-bound Se was the dominant fractions. The average concentrations (mg kg−1) of Se in the paddy tissues were 0.069 in seed, 0.263 in root, 0.09 in stalk, and 0.17 in leaf. The organic matter-bound Se had a significant indirect effect on Se accumulation in paddy tissues. In conclusion, organic matter-bound Se was an important fraction and source of plant Se in agricultural soil.


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