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TIN-X v2: modernized architecture with REST
API for sustainability & interoperability
IDG Face2Face, Feb 26-27, 2019, Arlington, VA
New Architecture, TIN-X Version 2.0 (newdrugtargets.org)
● Thin, modern, responsive web app
● Tighter TCRD integration via MySQL
● Better automated for faster PubMed updates
● Dockerized for rapid, flexible, economical deployment
● Design patterned for replication and reuse.
Overview
● TIN-X = Target Importance and Novelty Explorer
● Bibliometric analytical method for prioritizing targets
● Data source: TCRD/Pharos
● Prototype developed into product -- DevOps
● Proposed informatics tools exemplar
● New architecture for sustainability
● New REST API for interoperability
● Version 2.0 released Feb 18, 2019
References:
1. TIN-X: Target Importance and Novelty Explorer, DC Cannon, JJ Yang, SL
Mathias, O Ursu, S Mani, A Waller, SC Schürer, LJ Jensen, LA Sklar, CG
Bologa, TI Oprea, Bioinformatics, 2017, btx200, doi:
10.1093/bioinformatics/btx200.
2. NIH Strategic Plan for Data Science,
https://grants.nih.gov/grants/rfi/NIH-Strategic-Plan-for-Data-Science.pdf.
NEW: REST API, Swagger powered, public
TIN-X API Intro, via Jupyter, Google Colaboratory
TIN-X v2 for Type 2 diabetes mellitus
DTO/DO
Disease
Ontology
Jeremy Yang1
, Daniel Cannon2
, Cristian Bologa1
, Stephen Mathias1
, Lars Juhl Jensen3
, Stephan Schürer4
, Dušica Vidović4
, and Tudor Oprea1
1
University of New Mexico, Albuquerque, NM, USA; 2
Iterative Consulting, LLC, Albuquerque, NM, USA; 3
Novo Nordisk Center for Protein Research, University of Denmark, Copenhagen,
Denmark; 4
University of Miami, Miami, FL, USA
History, Background, Contributions
TIN-X is designed to prioritize and visualize associations between proteins and
diseases, from scientific literature (PubMed) text mining by JensenLab, via TCRD,
and organized by Drug Target Ontology (DTO) based disease and protein
classifications. TIN-X was initially conceived and prototyped by Cristian Bologa, then
engineered as a full stack webapp by Daniel Cannon, deployed via AWS. Motivated
by its success and perceived value to researchers, TIN-X has been continually
maintained, updated, and improved. Recently, TIN-X has undergone a major revision
to version 2.0, designed and implemented by Iterative Consulting, LLC, co-founded
by Daniel Cannon. The new architecture conforms to modern software engineering
standards, includes a Swagger/Django REST API, D3 thin client, and tight integration
with TCRD. Updates and deployment automation employs Docker and AWS (EC2,
S3, CloudFront). Source code is managed via Bitbucket and GitHub. The
improvements address the Resource Sharing Plan of KMC, and NIH policies and
principles concerning digital resource sharing (e.g. FAIR) as emphasized by the NIH
Strategic Plan for Data Science. Specifically, the new architecture
● Facilitates timely updates.
● Facilitates code support, maintenance, and further development.
● Facilitates clients with API access to TIN-X results.
● Provides transparency and reproducibility of workflow protocols.
● Serves as exemplar for IDG KMC based informatics and analytics tools.
In addition, the development and evolution of TIN-X from research prototype to
enterprise component is a proposed DevOps design pattern.
TDL
colors
IDG
families
Drilldown &
linkout to
PubMed
articles
Share/bookmark & export data
api.newdrugtargets.org
This work was supported by US National Institutes of Health (grants U54 CA189205 and U24 224370), Illuminating the Druggable Genome Knowledge Management Center (IDG KMC),
and by the Novo Nordisk Foundation (grant number NNF14CC0001).

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TIN-X v2: modernized architecture with REST API

  • 1. TIN-X v2: modernized architecture with REST API for sustainability & interoperability IDG Face2Face, Feb 26-27, 2019, Arlington, VA New Architecture, TIN-X Version 2.0 (newdrugtargets.org) ● Thin, modern, responsive web app ● Tighter TCRD integration via MySQL ● Better automated for faster PubMed updates ● Dockerized for rapid, flexible, economical deployment ● Design patterned for replication and reuse. Overview ● TIN-X = Target Importance and Novelty Explorer ● Bibliometric analytical method for prioritizing targets ● Data source: TCRD/Pharos ● Prototype developed into product -- DevOps ● Proposed informatics tools exemplar ● New architecture for sustainability ● New REST API for interoperability ● Version 2.0 released Feb 18, 2019 References: 1. TIN-X: Target Importance and Novelty Explorer, DC Cannon, JJ Yang, SL Mathias, O Ursu, S Mani, A Waller, SC Schürer, LJ Jensen, LA Sklar, CG Bologa, TI Oprea, Bioinformatics, 2017, btx200, doi: 10.1093/bioinformatics/btx200. 2. NIH Strategic Plan for Data Science, https://grants.nih.gov/grants/rfi/NIH-Strategic-Plan-for-Data-Science.pdf. NEW: REST API, Swagger powered, public TIN-X API Intro, via Jupyter, Google Colaboratory TIN-X v2 for Type 2 diabetes mellitus DTO/DO Disease Ontology Jeremy Yang1 , Daniel Cannon2 , Cristian Bologa1 , Stephen Mathias1 , Lars Juhl Jensen3 , Stephan Schürer4 , Dušica Vidović4 , and Tudor Oprea1 1 University of New Mexico, Albuquerque, NM, USA; 2 Iterative Consulting, LLC, Albuquerque, NM, USA; 3 Novo Nordisk Center for Protein Research, University of Denmark, Copenhagen, Denmark; 4 University of Miami, Miami, FL, USA History, Background, Contributions TIN-X is designed to prioritize and visualize associations between proteins and diseases, from scientific literature (PubMed) text mining by JensenLab, via TCRD, and organized by Drug Target Ontology (DTO) based disease and protein classifications. TIN-X was initially conceived and prototyped by Cristian Bologa, then engineered as a full stack webapp by Daniel Cannon, deployed via AWS. Motivated by its success and perceived value to researchers, TIN-X has been continually maintained, updated, and improved. Recently, TIN-X has undergone a major revision to version 2.0, designed and implemented by Iterative Consulting, LLC, co-founded by Daniel Cannon. The new architecture conforms to modern software engineering standards, includes a Swagger/Django REST API, D3 thin client, and tight integration with TCRD. Updates and deployment automation employs Docker and AWS (EC2, S3, CloudFront). Source code is managed via Bitbucket and GitHub. The improvements address the Resource Sharing Plan of KMC, and NIH policies and principles concerning digital resource sharing (e.g. FAIR) as emphasized by the NIH Strategic Plan for Data Science. Specifically, the new architecture ● Facilitates timely updates. ● Facilitates code support, maintenance, and further development. ● Facilitates clients with API access to TIN-X results. ● Provides transparency and reproducibility of workflow protocols. ● Serves as exemplar for IDG KMC based informatics and analytics tools. In addition, the development and evolution of TIN-X from research prototype to enterprise component is a proposed DevOps design pattern. TDL colors IDG families Drilldown & linkout to PubMed articles Share/bookmark & export data api.newdrugtargets.org This work was supported by US National Institutes of Health (grants U54 CA189205 and U24 224370), Illuminating the Druggable Genome Knowledge Management Center (IDG KMC), and by the Novo Nordisk Foundation (grant number NNF14CC0001).