Integration of Data and Phenotypic Data Within a Unified Extensible Multimodal Framework.

TitleIntegration of Data and Phenotypic Data Within a Unified Extensible Multimodal Framework.
Publication TypeJournal Article
Year of Publication2018
AuthorsDas S, Boucher XLecours, Rogers C, Makowski C, Chouinard-Decorte F, Klein KOros, Beck N, Rioux P, Brown ST, Mohaddes Z, Zweber C, Foing V, Forest M, O'Donnell KJ, Clark J, Meaney MJ, Greenwood CMT, Evans AC
JournalFront Neuroinform
Volume12
Pagination91
Date Published2018
ISSN1662-5196
Abstract

Analysis of "" data is often a long and segmented process, encompassing multiple stages from initial data collection to processing, quality control and visualization. The cross-modal nature of recent genomic analyses renders this process challenging to both automate and standardize; consequently, users often resort to manual interventions that compromise data reliability and reproducibility. This in turn can produce multiple versions of datasets across storage systems. As a result, scientists can lose significant time and resources trying to execute and monitor their analytical workflows and encounter difficulties sharing versioned data. In 2015, the Ludmer Centre for Neuroinformatics and Mental Health at McGill University brought together expertise from the Douglas Mental Health University Institute, the Lady Davis Institute and the Montreal Neurological Institute (MNI) to form a genetics/epigenetics working group. The objectives of this working group are to: (i) design an automated and seamless process for (epi)genetic data that consolidates heterogeneous datasets into the LORIS open-source data platform; (ii) streamline data analysis; (iii) integrate results with provenance information; and (iv) facilitate structured and versioned sharing of pipelines for optimized reproducibility using high-performance computing (HPC) environments via the CBRAIN processing portal. This article outlines the resulting and its benefits, specifically, the ability to: (i) integrate multiple types of biological and multi-modal datasets (imaging, clinical, demographics and behavioral); (ii) automate the process of launching analysis pipelines on HPC platforms; (iii) remove the bioinformatic barriers that are inherent to this process; (iv) ensure standardization and transparent sharing of processing pipelines to improve computational consistency; (v) store results in a queryable web interface; (vi) offer visualization tools to better view the data; and (vii) provide the mechanisms to ensure usability and reproducibility. This framework for workflows facilitates brain research discovery by reducing human error through automation of analysis pipelines and seamless linking of multimodal data, allowing investigators to focus on research instead of data handling.

DOI10.3389/fninf.2018.00091
Alternate JournalFront Neuroinform
PubMed ID30631270
PubMed Central IDPMC6315165

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