Journal:Design, implementation and operation of a multimodality research imaging informatics repository

From LIMSWiki
Revision as of 19:38, 12 January 2016 by Shawndouglas (talk | contribs) (Added content. Saving and adding more.)
Jump to navigationJump to search
Full article title Design, implementation and operation of a multimodality research imaging informatics repository
Journal Health Information Science and Systems
Author(s) Nguyen, Toan D.; Raniga, Parnesh; Barnes, David G.; Egan, Gary F.
Author affiliation(s) Monash University, CSIRO
Primary contact Email:
Year published 2015
Volume and issue 3 (Suppl 1)
Page(s) S6
DOI 10.1186/2047-2501-3-S1-S6
ISSN 2047-2501
Distribution license Creative Commons Attribution 4.0 International
Download (PDF)


Background: Biomedical imaging research increasingly involves acquiring, managing and processing large amounts of distributed imaging data. Integrated systems that combine data, meta-data and workflows are crucial for realising the opportunities presented by advances in imaging facilities.

Methods: This paper describes the design, implementation and operation of a multi-modality research imaging data management system that manages imaging data obtained from biomedical imaging scanners operated at Monash Biomedical Imaging (MBI), Monash University in Melbourne, Australia. In addition to Digital Imaging and Communications in Medicine (DICOM) images, raw data and non-DICOM biomedical data can be archived and distributed by the system. Imaging data are annotated with meta-data according to a study-centric data model and, therefore, scientific users can find, download and process data easily.

Results: The research imaging data management system ensures long-term usability, integrity inter-operability and integration of large imaging data. Research users can securely browse and download stored images and data, and upload processed data via subject-oriented informatics frameworks including the Distributed and Reflective Informatics System (DaRIS), and the Extensible Neuroimaging Archive Toolkit (XNAT).


Modern clinical and biomedical research is increasingly reliant on imaging across a range of electromagnetic and acoustic wavelengths.[1][2][3] Contemporary studies now routinely collect images from more than one type of instrumentation - multi-modal studies[4] - and strive to obtain high spatial and/or temporal resolution data. Multi-modal datasets provide complementary information[5] and enable sophisticated, multivariate analysis, while high-resolution datasets provide insight that was not possible only a few years ago. Extremely large multi-modal imaging studies can result in terabyte (TB) size data collections[6], although most research studies generate data in the megabyte (MB) to gigabyte (GB) range per subject.

The data volume per subject is multiplied by the increasing number of subjects per study. Many of today's high profile biomedical imaging studies have hundreds to thousands of participants.[7][8][9] Furthermore, many of these studies are longitudinal in nature and thus collect imaging data at multiple time points per subject. This multiplier effect results in a large collection of data that must be recorded per subject. Along with the imaging data, non-imaging and meta-data may also collected and should be stored and directly associated with the image data, especially if the data will be mined and/or shared.[10]

Clinical informatics systems such as clinical picture archiving and communication systems (PACS) are commonplace[11], but their design, specifically for clinical settings, precludes effective use in a research environment. For example, the majority of PACS store data only in the Digital Imaging and Communications in Medicine (DICOM) format. The DICOM format consists of a binary header of tag/value pairs. The tags (2 bytes) are keys but the descriptions of tags are stored independently in DICOM dictionaries and not in the data itself. The type of the value is contained in the tag/value pair, which enables the accurate reading of the data and meta-data. Binary data is stored as a tag/value pair.

Neuroimaging processing and analysis is however typically conducted using a myriad of proprietary formats such as MINC[12], MRTrix image File (mif)[13] and Freesurfer File Format (mgh).[14] Recently, the Neuroimaging Informatics Technology Initiative (NIfTI) has provided a reference file format that is starting to become universally accepted and utilised.[15] The reason for the use of non-DICOM format was that traditionally, DICOM data for imaging modalities was stored as a single 2D image per file. For large 3D datasets, this means a lot of repetition of meta-data and slow reading of the data. The newer DICOM 3.0 format has alleviated some of these performance issues but at the expense of simplicity. Moreover the DICOM standards define a set of required meta-data based on the acquisition modality. Many of these required fields do not make sense for processed data and other relevant meta-data would need to be stored as DICOM tags which may not be understandable by all software.

The limitations of a solitary supported image format notwithstanding, it is not possible to keep track of and provide provenance for processed image or sensor data, which is usually in non-DICOM formats such as the NIfTI format. While some proprietary formats include support for meta-data by storing key value pairs, no such ability is present in NIfTI for example. Examples of such meta-data include the diffusion direction table that was used to acquire diffusion magnetic resonance imaging (MRI), control/tag/reference flags for arterial spin labelling images, various reference images and parameters for magnetic resonance (MR) spectroscopy data. Most of this meta-data is encoded as tag/values in the DICOM header but is lost on conversion to other types. Other types of meta-data include descriptions of the type of data (e.g. brain gray matter segmentation) and of the tools and/or pipelines that generated the data. Typically the later is done by utilising common naming conventions. However this can lead to ambiguity if all users and all tools do not implement the convention. Moreover, only a limited amount of information can be stored in this format.

Furthermore the most commonly used DICOM data model is a subject (patient)-centric model. While the DICOM standard allows for a data model that is project-centric, such as the clinical trial information entity, but in practise, PACS usually do not support this feature. The patient or subject centric model in DICOM has been developed with the clinic in mind. Each subject/patient is assumed to be independent of the other with little in common and it is not possible to group subjects together. Moreover the DICOM model does not inherently support the idea of longitudinal studies where the same patient is repeatedly scanned, some time interval apart. The ability to organise and quickly access data based on a project centric data model is essential to research applications which are project centric by nature.

Apart from the need for storing acquired data, research projects require the storage of post-processed data. The raw data is put through various automated and semi-automated algorithms to produce images and well as other data types and statistics. A description of all the processing steps and parameters needs to be stored with the data in order to keep track of how the final data was obtained. This provenance information is crucial in also keeping track of potential changes that may have occurred over different processing runs as well to search for data across projects that maybe similarly acquired and processed.

The need for raw data collection and management, as well the accurate recording of data provenance of processed data, for large biomedical imaging research studies, has resulted in the recent development of software packages, unlike clinical picture archiving and communication systems (PACS), that are designed specifically for research studies.[16][17][18][19] Along with the collection and storage of the primary data, these systems have been designed to store processed data as well as provenance information regarding the processing steps[20], although tight integration of the provenance information within the informatics platform is still under active research and development. Currently, in many such systems, provenance information is just another piece of meta-data that is optional. It's formatting and contents are up to the users. With tight integration, the province information would be required, would follow a known format and be ingestible by the system. The difficulty with this is that no universal standard for provenance in medical imaging exists either. Processed data storage and access is a critically important area since the size of processed datasets can be many tens of times larger than the original dataset, and in many cases are expensive to recompute.

While informatics platforms for medical imaging are available, implementing an informatics strategy at a research-focused imaging facility is a challenging task. It depends on integrating acquisition systems (modalities) with good imaging informatics practise realised as a data model-based system, underpinned by archival-grade data storage infrastructure, and complete with functional and practical user interfaces. Most of the informatics platforms are oriented around the Project-Subject-Study-Data (PSSD) model but differ slightly in their implementation details and access methods. In this paper we describe the implementation of the informatics systems and data flows at the Monash Biomedical Imaging (MBI) facility at Monash University. Moreover we describe how we developed a set of tools and standard practises to that have enabled the efficient storage and access of biomedical imaging data.



We start by considering a concise listing of the main requirements of an imaging informatics system at Monash Biomedical Imaging. A full requirements specification would be too long for this paper; instead, we focus on the core capabilities needed to support a generic multi-modal, multi-subject, longitudinal study - the core research activity we endeavour to enable and support.

1) imaging data from DICOM capable modalities (e.g. MRI) must be, to a large extent, automatically routed from the point of acquisition to the imaging informatics system;

2) imaging and non-imaging data from non-DICOM capable modalities (e.g. EEG) must be, to a large extent, easily manually uploaded to the imaging informatics system or uploaded using scripts and command line tools;

3) imaging and non-imaging data and meta-data must be stored on secure, reliable, research grade backed-up storage;

4) upon ingest of DICOM-format images, standard meta-data should, to a large extent, be automatically extracted ("harvested") from the DICOM files and recorded in the imaging informatics system;

5) human imaging data must be accessible by standard radiology software for review by the MBI radiologist;

6) imaging and non-imaging data must be organised in a study centric fashion, supporting multi-modal and longitudinal image collections per study subject;

7) an end user tool should exist to aid users in defining the set of meta-data to associate with a study and its subjects, and in defining the data acquisition(s) that comprise the study;

8) all data must be uniquely identifiable without the need for real subject names or identifying information other than date of birth and gender;

9) imaging and non-imaging data and meta-data must be available via a secure web portal to the owner (research leader) and their delegate/s;

10) imaging and non-imaging data must be transferable from within the secure web portal to the accessing workstation ("download") or to Monash University's high performance computing facility MASSIVE ("transfer");

11) users should be able to manually package and upload processed data and record provenance (e.g. link to the source data set/s); and

12) a command-line based tool must be available that enables search of the image informatics system, and upload and download of data collections, for use in batch processing workflows.

Informatics systems and data model

At MBI we currently have two informatics platforms deployed, namely DaRIS[17] and XNAT.[16] DaRIS is a framework built on the top of Mediaflux (Architecta Pty Ltd, Melbourne, Australia), a commercial media asset management system, and is specifically designed for medical imaging data. Assets in Mediaflux are associated with XML meta-data that can be automatically extracted from data or input manually by users. Mediaflux provides a set of services for data management, such as finding, storing and retrieving assets, archiving and handling large data, and data analysis and transformation. To protect data, Mediaflux implements a strong authorisation model in which role based authorisation is used to access to data and each repository has independent access control. DaRIS builds on these capabilities by imposing a data model and a set of methods.

The data model adopted at MBI is the project-subject-study-data (PSSD) model that is used in DaRIS, and although the elements of the XNAT data model are named differently, they can be mapped directly to the PSSD data model (Figure 1). The PSSD data model is a hierarchical data model that is anchored at the project level, unlike the DICOM data model. Each object in the model has an independent citable identifier that allows the object to be referenced uniquely in a distributed environment, with the uniqueness property in DaRIS enforced by Mediaflux. A method declares what meta-data must and optionally can be entered when a new entity (project, subject, study or data set) is created. New methods can be created using Tool Command Language (TCL) script which Mediaflux natively supports, or Method Builder, which is a Mediaflux web interface plugin developed for us by the Victorian e-Research Strategic Initiative (VeRSI).

Fig1 Nguyen HealthInfoSciSys2015 3-Suppl1.jpg

Figure 1. The data models of DaRIS and XNAT = illustrate the one to one correspondence between two models. The data model diverges slightly at the Scan/Data level in that XNAT has specific subclasses (Reconstruction and Image Assessment) for post-processed data deriving from Scan whereas this information is contained in the meta-data and methods in DaRIS. Study and experiment are the same concept.

XNAT, a free Open Source Software imaging informatics platform, is designed for common management and productivity tasks for imaging and associated data. It has been developed based on a three tiered architecture including a data archive, a user interface and a middleware "engine". The XNAT data model is equivalent to the DaRIS one with project-subject-experiment-data forming the hierarchy. While XNAT does not have an explicit method type like DaRIS, extra data and meta-data can be entered into XNAT. Researchers can work with their data easily using the XNAT web interface to upload data using data entry forms, perform data-type-specific search, view detailed reports and experimental data and access research workflows. Like DaRIS, XNAT has an in-built DICOM server that can be programmed to archive incoming data based on values in specified DICOM tags. XNAT has an HTTP based REST API for querying, retrieving and storing data.

The XNAT and DaRIS data-models diverge slightly at the Scan/Data level in that XNAT has specific subclasses (Reconstruction and Image Assessment) for post-processed data deriving from Scan whereas this information is contained in the meta-data and methods in DaRIS. For primary data, the data models are equivalent. For processed data, XNAT stores the data within reconstructions and image assessments (we only utilise the later) which is a subclass of scan. In DaRIS, no such distinction exists and the associated meta-data at the Data level reflects the difference between primary and processed data.

In order to simply the access to the systems, hide differences between data models and enforce some meta-data entry, we have developed python classes that map onto the PSSD model for interacting with DaRIS and XNAT. These classes hide the lower level interaction from the user and allow them to utilise both in a similar manner. Moreover, the python tools enforce the entry of certain meta-data. For example, provenance information needs to be attached to every processed dataset before it is uploaded. Similarly a description and version of the tools or workflow that produced the dataset needs to be entered.

The python tools are currently being utilised for automated workflows. These workflows are scripts/programs that are designed to download appropriate datasets from projects, perform a task and uploaded processed data back onto the informatics system. An example of this is the Freesurfer recon_all workflow[14] that segments brain MRI images. Another example is the preprocessing of functional MRI data to correct for head-motion and distortion.

Automatic data flows

The automatic data flows in the MBI imaging informatics system are shown in Figure 2. Data sources (i.e. scanners) are shown on the left. The Syngo-via server is a clinical PACS system and radiological reporting tool (Siemens Via server, Siemens, Erlangan, Germany). The Monash petascale Large Research Data Storage (LaRDS) system provides the networked, high performance storage and backup system. DaRIS and XNAT are the front-end research informatics platforms described in the previous section that we currently use and support.

Fig2 Nguyen HealthInfoSciSys2015 3-Suppl1.jpg

Figure 2. The acquisition and automated data flows through the current system. Data from the scanners are pushed directly to DaRIS or to Syngo-via Server and then forwarded to XNAT or DaRIS.

DICOM data from human subjects (control or otherwise) MRI scans are sent from the scanner to the Syngo-via server and reviewed by a radiologist for incidental and adverse findings. This data route currently is only used for our 3 Telsa Siemens Skyra MRI scanner (Siemens, Erlangan Germany) but future facilities acquiring imaging data from human volunteers will join into this path. From the Syngo-via server, data is forwarded to one or both research informatics platforms (DaRIS and XNAT currently, but others easily supported) based on the values in specified DICOM tags. All DICOM data arriving at the Syngo-via server are simply forwarded to a secondary DICOM server running on Mediaflux for "last resort" archiving. Whilst DaRIS is our principal (and default) repository for biomedical imaging data and meta-data, XNAT is available where it presents an advantage or preference for the users.

It should be noted that all subjects (human and non-human) are assigned unique identifiers (subject identifier and scan identifier) prior to scanning. Identifying and other associated meta-data for human subjects is stored in a separately maintained, secure, administrative database. For human subjects, no identifying data is stored in the DICOM images apart from gender and date of birth. If a subject must be identified (e.g. for reporting of incidental findings), it is done so via the mapping in the secure administrative database real identities.

A normal clinical PACS operates only on DICOM images via DICOM communication. In a research imaging data management environment raw data (pre-image reconstruction) and non-DICOM image data must also be managed, since pre-clinical imaging scanners do not in general implement full DICOM support. Data from the 9.4T and microPET/CT scanners are sent directly to the associated platforms e.g. DaRIS either automatically via export of DICOMS or semi-automatic uploads of proprietary formats using scripts. Raw data from the 3T Skyra scanner is also sent to a server and then archived to LaRDS on request from projects. This can then be reconstructed and post-processed with different algorithms to those available on the scanner.

For large datasets that are required to be accessed often, digital object identifiers (DOIs) and digital handles are being implemented in DaRIS as long-lived references to the datasets.


  1. Lauterbur, P.C. (1973). "Image Formation by Induced Local Interactions: Examples Employing Nuclear Magnetic Resonance". Nature 242 (5394): 190-1. doi:10.1038/242190a0. 
  2. Wang, X.; Pang, Y.; Ku, G.; Xie, X.; Stoica, G.; Wang, L.V. (2003). "Noninvasive laser-induced photoacoustic tomography for structural and functional in vivo imaging of the brain". Nature Biotechnology 21 (7): 803-6. doi:10.1038/nbt839. PMID 12808463. 
  3. Ledley, R.S.; Di Chiro, G.; Luessenhop, A.J.; Twigg, H.L. (1974). "Computerized transaxial x-ray tomography of the human body". Science 186 (4160): 207-12. doi:10.1126/science.186.4160.207. PMID 4606376. 
  4. Pichler, B.J.; Kolb, A.; Nägele, T.; Schlemmer, H.-P. (2010). "PET/MRI: Paving the Way for the Next Generation of Clinical Multimodality Imaging Applications". Journal of Nuclear Medicine 51 (3): 333-6. doi:10.2967/jnumed.109.061853. PMID 20150252. 
  5. Cherry, S.R. (2009). "Multimodality Imaging: Beyond PET/CT and SPECT/CT". Seminars in Nuclear Medicine 39 (5): 348-53. doi:10.1053/j.semnuclmed.2009.03.001. PMC PMC2735449. PMID 19646559. 
  6. Amunts, K.; Lepage, C.; Borgeat, L. et al. (2013). "BigBrain: An Ultrahigh-Resolution 3D Human Brain Model". Science 340 (6139): 1472-5. doi:10.1126/science.1235381. PMID 23788795. 
  7. Ellis, K.A.; Bush, A.I.; Darby, D. et al. (2009). "The Australian Imaging, Biomarkers and Lifestyle (AIBL) study of aging: methodology and baseline characteristics of 1112 individuals recruited for a longitudinal study of Alzheimer's disease". International Psychogeriatrics 21 (4): 672-87. doi:10.1017/S1041610209009405. PMID 19470201. 
  8. Mueller, S.G.; Weiner, M.W.; Thal, L.J. et al. (2005). "Ways toward an early diagnosis in Alzheimer's disease: the Alzheimer's Disease Neuroimaging Initiative (ADNI)". Alzheimer's & Dementia 1 (1): 55–66. doi:10.1016/j.jalz.2005.06.003. PMC PMC1864941. PMID 17476317. 
  9. Hofman, A.; Breteler, M.M.B.; van Duijn, C.M. et al. (2009). "The Rotterdam Study: 2010 objectives and design update". European Journal of Epidemiology 24 (9): 553-72. doi:10.1007/s10654-009-9386-z. PMC PMC2744826. PMID 19728115. 
  10. Linkert, M.; Rueden, C.T.; Allan, C. et al. (2010). "Metadata matters: access to image data in the real world". Journal of Cell Biology 189 (5): 777-82. doi:10.1083/jcb.201004104. PMC PMC2878938. PMID 20513764. 
  11. Bryan, S.; Weatherburn, G.C.; Watkins, J.R.; Buxton, M.J. et al. (1999). "The benefits of hospital-wide picture archiving and communication systems: a survey of clinical users of radiology services". British Journal of Radiology 72 (857): 469-78. doi:10.1259/bjr.72.857.10505012. PMID 10505012. 
  12. "BIC - The McConnell Brain Imaging Centre: Home Page". McConnell Brain Imaging Centre. Retrieved 17 June 2014. 
  13. Tournier, J.-D.; Calamante, F.; Connelly, A. et al. (2012). "MRtrix: Diffusion tractography in crossing fiber regions". International Journal of Imaging Systems and Technology 22 (1): 53–66. doi:10.1002/ima.22005. 
  14. 14.0 14.1 "FreeSurfer". Harvard University. Retrieved 17 June 2014. 
  15. "NIfTI: Neuroimaging Informatics Technology Initiative". Data Format Working Group. Retrieved 17 June 2014. 
  16. 16.0 16.1 Marcus, D.S.; Olsen, T.R.; Ramaratnam, M.; Buckner, R.L. et al. (2007). "The Extensible Neuroimaging Archive Toolkit: an informatics platform for managing, exploring, and sharing neuroimaging data". Neuroinformatics 5 (1): 11-34. doi:10.1385/NI:5:1:11. PMID 17426351. 
  17. 17.0 17.1 Lohrey, J.M.; Killeen, N.E.B.; Egan, G.F. et al. (2009). "An integrated object model and method framework for subject-centric e-Research applications". Frontiers in Neuroinformatics 3: 19. doi:10.3389/neuro.11.019.2009. PMC PMC2715266. PMID 19636389. 
  18. Book, G.A.; Anderson, B.M.; Stevens, M.C.; Glahn, D.C.; Assaf, M.; Pearlson, G.D. (2013). "Neuroinformatics Database (NiDB)--a modular, portable database for the storage, analysis, and sharing of neuroimaging data". Neuroinformatics 11 (4): 495-505. doi:10.1007/s12021-013-9194-1. PMC PMC3864015. PMID 23912507. 
  19. Van Horn, J.D.; Toga, A.W. (2009). "Is it Time to Re-Prioritize Neuroimaging Databases and Digital Repositories?". NeuroImage 47 (4): 1720-34. doi:10.1016/j.neuroimage.2009.03.086. PMC PMC2754579. PMID 19371790. 
  20. MacKenzie-Graham, A.J.; Van Horn, J.D.; Woods, R.P.; Crawford, K.L.; Toga, A.W. (2008). "Provenance in neuroimaging". NeuroImage 42 (1): 178-95. doi:10.1016/j.neuroimage.2008.04.186. PMC PMC2664747. PMID 18519166. 


This presentation is faithful to the original, with only a few minor changes to presentation. In some cases important information was missing from the references, and that information was added. In one case a direct reference to a citation number was changed to reference the author names instead.