A review of connectivity map and computational approaches in pharmacogenomics
Abstract Large-scale perturbation databases, such as Connectivity Map (CMap) or Library of Integrated Network-based Cellular Signatures (LINCS), provide enormous opportunities for computational pharmacogenomics and drug design. A reason for this is that in contrast to classical pharmacology focusing...
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Published in | Briefings in bioinformatics Vol. 19; no. 3; pp. 506 - 523 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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England
Oxford University Press
01.05.2018
Oxford Publishing Limited (England) |
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Abstract | Abstract
Large-scale perturbation databases, such as Connectivity Map (CMap) or Library of Integrated Network-based Cellular Signatures (LINCS), provide enormous opportunities for computational pharmacogenomics and drug design. A reason for this is that in contrast to classical pharmacology focusing at one target at a time, the transcriptomics profiles provided by CMap and LINCS open the door for systems biology approaches on the pathway and network level. In this article, we provide a review of recent developments in computational pharmacogenomics with respect to CMap and LINCS and related applications. |
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AbstractList | Large-scale perturbation databases, such as Connectivity Map (CMap) or Library of Integrated Network-based Cellular Signatures (LINCS), provide enormous opportunities for computational pharmacogenomics and drug design. A reason for this is that in contrast to classical pharmacology focusing at one target at a time, the transcriptomics profiles provided by CMap and LINCS open the door for systems biology approaches on the pathway and network level. In this article, we provide a review of recent developments in computational pharmacogenomics with respect to CMap and LINCS and related applications. Large-scale perturbation databases, such as Connectivity Map (CMap) or Library of Integrated Network-based Cellular Signatures (LINCS), provide enormous opportunities for computational pharmacogenomics and drug design. A reason for this is that in contrast to classical pharmacology focusing at one target at a time, the transcriptomics profiles provided by CMap and LINCS open the door for systems biology approaches on the pathway and network level. In this article, we provide a review of recent developments in computational pharmacogenomics with respect to CMap and LINCS and related applications.Large-scale perturbation databases, such as Connectivity Map (CMap) or Library of Integrated Network-based Cellular Signatures (LINCS), provide enormous opportunities for computational pharmacogenomics and drug design. A reason for this is that in contrast to classical pharmacology focusing at one target at a time, the transcriptomics profiles provided by CMap and LINCS open the door for systems biology approaches on the pathway and network level. In this article, we provide a review of recent developments in computational pharmacogenomics with respect to CMap and LINCS and related applications. Abstract Large-scale perturbation databases, such as Connectivity Map (CMap) or Library of Integrated Network-based Cellular Signatures (LINCS), provide enormous opportunities for computational pharmacogenomics and drug design. A reason for this is that in contrast to classical pharmacology focusing at one target at a time, the transcriptomics profiles provided by CMap and LINCS open the door for systems biology approaches on the pathway and network level. In this article, we provide a review of recent developments in computational pharmacogenomics with respect to CMap and LINCS and related applications. |
Author | Yli-Harja, Olli Emmert-Streib, Frank Glazko, Galina Haibe-Kains, Benjamin Ghoraie, Laleh Soltan Zhang, Shu-Dong Dehmer, Matthias Musa, Aliyu |
AuthorAffiliation | 5 Computational Systems Biology, Department of Signal Processing, Tampere University of Technology, Tampere, Finland 7 Department of Medical Biophysics, University of Toronto, Toronto, ON, Canada 9 Ontario Institute of Cancer Research, Toronto, ON, Canada 6 Institute for Bioinformatics and Translational Research, UMIT- The Health and Life Sciences University, Eduard Wallnoefer Zentrum 1, Hall in Tyrol, Austria 4 University of Rochester Department of Biostatistics and Computational Biology, Rochester, New York, USA 1 Predictive Medicine and Analytics Lab, Department of Signal Processing, Tampere University of Technology, Tampere, Finland 3 Northern Ireland Centre for Stratified Medicine, Biomedical Sciences Research Institute, University of Ulster, C-TRIC Building, Altnagelvin Area Hospital, Glenshane Road, Derry/Londonderry, Northern Ireland, UK 2 Bioinformatics and Computational Genomics Laboratory, Princess Margaret Cancer Center, University Health Network, Toronto, ON, Canada 8 Department o |
AuthorAffiliation_xml | – name: 4 University of Rochester Department of Biostatistics and Computational Biology, Rochester, New York, USA – name: 8 Department of Computer Science, University of Toronto, Toronto, ON, Canada – name: 9 Ontario Institute of Cancer Research, Toronto, ON, Canada – name: 2 Bioinformatics and Computational Genomics Laboratory, Princess Margaret Cancer Center, University Health Network, Toronto, ON, Canada – name: 5 Computational Systems Biology, Department of Signal Processing, Tampere University of Technology, Tampere, Finland – name: 6 Institute for Bioinformatics and Translational Research, UMIT- The Health and Life Sciences University, Eduard Wallnoefer Zentrum 1, Hall in Tyrol, Austria – name: 7 Department of Medical Biophysics, University of Toronto, Toronto, ON, Canada – name: 1 Predictive Medicine and Analytics Lab, Department of Signal Processing, Tampere University of Technology, Tampere, Finland – name: 3 Northern Ireland Centre for Stratified Medicine, Biomedical Sciences Research Institute, University of Ulster, C-TRIC Building, Altnagelvin Area Hospital, Glenshane Road, Derry/Londonderry, Northern Ireland, UK |
Author_xml | – sequence: 1 givenname: Aliyu surname: Musa fullname: Musa, Aliyu email: frank.emmert-streib@tut.fi organization: Predictive Medicine and Analytics Lab, Department of Signal Processing, Tampere University of Technology, Tampere, Finland – sequence: 2 givenname: Laleh Soltan surname: Ghoraie fullname: Ghoraie, Laleh Soltan organization: Bioinformatics and Computational Genomics Laboratory, Princess Margaret Cancer Center, University Health Network, Toronto, ON, Canada – sequence: 3 givenname: Shu-Dong surname: Zhang fullname: Zhang, Shu-Dong organization: Northern Ireland Centre for Stratified Medicine, Biomedical Sciences Research Institute, University of Ulster, C-TRIC Building, Altnagelvin Area Hospital, Glenshane Road, Derry/Londonderry, Northern Ireland, UK – sequence: 4 givenname: Galina surname: Glazko fullname: Glazko, Galina organization: University of Rochester Department of Biostatistics and Computational Biology, Rochester, New York, USA – sequence: 5 givenname: Olli surname: Yli-Harja fullname: Yli-Harja, Olli organization: Computational Systems Biology, Department of Signal Processing, Tampere University of Technology, Tampere, Finland – sequence: 6 givenname: Matthias surname: Dehmer fullname: Dehmer, Matthias organization: Institute for Bioinformatics and Translational Research, UMIT- The Health and Life Sciences University, Eduard Wallnoefer Zentrum 1, Hall in Tyrol, Austria – sequence: 7 givenname: Benjamin surname: Haibe-Kains fullname: Haibe-Kains, Benjamin organization: Bioinformatics and Computational Genomics Laboratory, Princess Margaret Cancer Center, University Health Network, Toronto, ON, Canada – sequence: 8 givenname: Frank surname: Emmert-Streib fullname: Emmert-Streib, Frank email: frank.emmert-streib@tut.fi organization: Predictive Medicine and Analytics Lab, Department of Signal Processing, Tampere University of Technology, Tampere, Finland |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28069634$$D View this record in MEDLINE/PubMed |
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Large-scale perturbation databases, such as Connectivity Map (CMap) or Library of Integrated Network-based Cellular Signatures (LINCS), provide... Large-scale perturbation databases, such as Connectivity Map (CMap) or Library of Integrated Network-based Cellular Signatures (LINCS), provide enormous... |
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SubjectTerms | Cellular communication Computational Biology - methods Computer applications Computer networks Databases, Factual drug design Drug development Gene Expression Profiling - methods Gene Regulatory Networks Humans Perturbation Pharmacogenetics Pharmacogenomics Pharmacology Small Molecule Libraries - pharmacology Transcriptome transcriptomics |
Title | A review of connectivity map and computational approaches in pharmacogenomics |
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