“EviMass”: A Literature Evidence-Based Miner for Human Microbial Associations

The importance of understanding microbe–microbe as well as microbe–disease associations is one of the key thrust areas in human microbiome research. High-throughput metagenomic and transcriptomic projects have fueled discovery of a number of new microbial associations. Consequently, a plethora of in...

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Main Authors: Divyanshu Srivastava, Krishanu D. Baksi, Bhusan K. Kuntal, Sharmila S. Mande
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-09-01
Series:Frontiers in Genetics
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fgene.2019.00849/full
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spelling doaj-1e1ed93099ed457db7dc1d81deca44682020-11-25T01:36:58ZengFrontiers Media S.A.Frontiers in Genetics1664-80212019-09-011010.3389/fgene.2019.00849466029“EviMass”: A Literature Evidence-Based Miner for Human Microbial AssociationsDivyanshu Srivastava0Krishanu D. Baksi1Krishanu D. Baksi2Bhusan K. Kuntal3Bhusan K. Kuntal4Bhusan K. Kuntal5Sharmila S. Mande6Bio-Sciences R&D Division, TCS Research, Tata Consultancy Services Ltd., Pune, IndiaBio-Sciences R&D Division, TCS Research, Tata Consultancy Services Ltd., Pune, IndiaSchool of Information Technology, Indian Institute of Technology Delhi, Delhi, IndiaBio-Sciences R&D Division, TCS Research, Tata Consultancy Services Ltd., Pune, IndiaChemical Engineering and Process Development Division, CSIR-National Chemical Laboratory, Pune, IndiaAcademy of Scientific and Innovative Research (AcSIR), CSIR-National Chemical Laboratory Campus, Pune, IndiaBio-Sciences R&D Division, TCS Research, Tata Consultancy Services Ltd., Pune, IndiaThe importance of understanding microbe–microbe as well as microbe–disease associations is one of the key thrust areas in human microbiome research. High-throughput metagenomic and transcriptomic projects have fueled discovery of a number of new microbial associations. Consequently, a plethora of information is being added routinely to biomedical literature, thereby contributing toward enhancing our knowledge on microbial associations. In this communication, we present a tool called “EviMass” (Evidence based mining of human Microbial Associations), which can assist biologists to validate their predicted hypotheses from new microbiome studies. Users can interactively query the processed back-end database for microbe–microbe and disease–microbe associations. The EviMass tool can also be used to upload microbial association networks generated from a human “disease–control” microbiome study and validate the associations from biomedical literature. Additionally, a list of differentially abundant microbes for the corresponding disease can be queried in the tool for reported evidences. The results are presented as graphical plots, tabulated summary, and other evidence statistics. EviMass is a comprehensive platform and is expected to enable microbiome researchers not only in mining microbial associations, but also enriching a new research hypothesis. The tool is available free for academic use at https://web.rniapps.net/evimass.https://www.frontiersin.org/article/10.3389/fgene.2019.00849/fullmicrobiomeliterature mininghuman diseaseweb servermicrobial association
collection DOAJ
language English
format Article
sources DOAJ
author Divyanshu Srivastava
Krishanu D. Baksi
Krishanu D. Baksi
Bhusan K. Kuntal
Bhusan K. Kuntal
Bhusan K. Kuntal
Sharmila S. Mande
spellingShingle Divyanshu Srivastava
Krishanu D. Baksi
Krishanu D. Baksi
Bhusan K. Kuntal
Bhusan K. Kuntal
Bhusan K. Kuntal
Sharmila S. Mande
“EviMass”: A Literature Evidence-Based Miner for Human Microbial Associations
Frontiers in Genetics
microbiome
literature mining
human disease
web server
microbial association
author_facet Divyanshu Srivastava
Krishanu D. Baksi
Krishanu D. Baksi
Bhusan K. Kuntal
Bhusan K. Kuntal
Bhusan K. Kuntal
Sharmila S. Mande
author_sort Divyanshu Srivastava
title “EviMass”: A Literature Evidence-Based Miner for Human Microbial Associations
title_short “EviMass”: A Literature Evidence-Based Miner for Human Microbial Associations
title_full “EviMass”: A Literature Evidence-Based Miner for Human Microbial Associations
title_fullStr “EviMass”: A Literature Evidence-Based Miner for Human Microbial Associations
title_full_unstemmed “EviMass”: A Literature Evidence-Based Miner for Human Microbial Associations
title_sort “evimass”: a literature evidence-based miner for human microbial associations
publisher Frontiers Media S.A.
series Frontiers in Genetics
issn 1664-8021
publishDate 2019-09-01
description The importance of understanding microbe–microbe as well as microbe–disease associations is one of the key thrust areas in human microbiome research. High-throughput metagenomic and transcriptomic projects have fueled discovery of a number of new microbial associations. Consequently, a plethora of information is being added routinely to biomedical literature, thereby contributing toward enhancing our knowledge on microbial associations. In this communication, we present a tool called “EviMass” (Evidence based mining of human Microbial Associations), which can assist biologists to validate their predicted hypotheses from new microbiome studies. Users can interactively query the processed back-end database for microbe–microbe and disease–microbe associations. The EviMass tool can also be used to upload microbial association networks generated from a human “disease–control” microbiome study and validate the associations from biomedical literature. Additionally, a list of differentially abundant microbes for the corresponding disease can be queried in the tool for reported evidences. The results are presented as graphical plots, tabulated summary, and other evidence statistics. EviMass is a comprehensive platform and is expected to enable microbiome researchers not only in mining microbial associations, but also enriching a new research hypothesis. The tool is available free for academic use at https://web.rniapps.net/evimass.
topic microbiome
literature mining
human disease
web server
microbial association
url https://www.frontiersin.org/article/10.3389/fgene.2019.00849/full
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