Abstract NRC publication: Yes
Background: With the decreasing cost of sequencing and the rapid developments in genomics technologies and protocols, the need for validated bioinformatics software that enables efficient large-scale data processing is growing. Findings: Here we present GenPipes, a flexible Python-based framework that facilitates the development and deployment of multi-step workflows optimized for high-performance computing clusters and the cloud. GenPipes already implements 12 validated and scalable pipelines for various genomics applications, including RNA sequencing, chromatin immunoprecipitation sequencing, DNA sequencing, methylation sequencing, Hi-C, capture Hi-C, metagenomics, and Pacific Biosciences long-read assembly. The software is available under a GPLv3 open source license and is continuously updated to follow recent advances in genomics and bioinformatics. The framework has already been configured on several servers, and a Docker image is also available to facilitate additional installations. Conclusions: GenPipes offers genomics researchers a simple method to analyze different types of data, customizable to their needs and resources, as well as the flexibility to create their own workflows.
AbstractList With the decreasing cost of sequencing and the rapid developments in genomics technologies and protocols, the need for validated bioinformatics software that enables efficient large-scale data processing is growing. Here we present GenPipes, a flexible Python-based framework that facilitates the development and deployment of multi-step workflows optimized for high-performance computing clusters and the cloud. GenPipes already implements 12 validated and scalable pipelines for various genomics applications, including RNA sequencing, chromatin immunoprecipitation sequencing, DNA sequencing, methylation sequencing, Hi-C, capture Hi-C, metagenomics, and Pacific Biosciences long-read assembly. The software is available under a GPLv3 open source license and is continuously updated to follow recent advances in genomics and bioinformatics. The framework has already been configured on several servers, and a Docker image is also available to facilitate additional installations. GenPipes offers genomics researchers a simple method to analyze different types of data, customizable to their needs and resources, as well as the flexibility to create their own workflows.
Background With the decreasing cost of sequencing and the rapid developments in genomics technologies and protocols, the need for validated bioinformatics software that enables efficient large-scale data processing is growing. Findings Here we present GenPipes, a flexible Python-based framework that facilitates the development and deployment of multi-step workflows optimized for high-performance computing clusters and the cloud. GenPipes already implements 12 validated and scalable pipelines for various genomics applications, including RNA sequencing, chromatin immunoprecipitation sequencing, DNA sequencing, methylation sequencing, Hi-C, capture Hi-C, metagenomics, and Pacific Biosciences long-read assembly. The software is available under a GPLv3 open source license and is continuously updated to follow recent advances in genomics and bioinformatics. The framework has already been configured on several servers, and a Docker image is also available to facilitate additional installations. Conclusions GenPipes offers genomics researchers a simple method to analyze different types of data, customizable to their needs and resources, as well as the flexibility to create their own workflows.
Abstract Background With the decreasing cost of sequencing and the rapid developments in genomics technologies and protocols, the need for validated bioinformatics software that enables efficient large-scale data processing is growing. Findings Here we present GenPipes, a flexible Python-based framework that facilitates the development and deployment of multi-step workflows optimized for high-performance computing clusters and the cloud. GenPipes already implements 12 validated and scalable pipelines for various genomics applications, including RNA sequencing, chromatin immunoprecipitation sequencing, DNA sequencing, methylation sequencing, Hi-C, capture Hi-C, metagenomics, and Pacific Biosciences long-read assembly. The software is available under a GPLv3 open source license and is continuously updated to follow recent advances in genomics and bioinformatics. The framework has already been configured on several servers, and a Docker image is also available to facilitate additional installations. Conclusions GenPipes offers genomics researchers a simple method to analyze different types of data, customizable to their needs and resources, as well as the flexibility to create their own workflows.
With the decreasing cost of sequencing and the rapid developments in genomics technologies and protocols, the need for validated bioinformatics software that enables efficient large-scale data processing is growing.BACKGROUNDWith the decreasing cost of sequencing and the rapid developments in genomics technologies and protocols, the need for validated bioinformatics software that enables efficient large-scale data processing is growing.Here we present GenPipes, a flexible Python-based framework that facilitates the development and deployment of multi-step workflows optimized for high-performance computing clusters and the cloud. GenPipes already implements 12 validated and scalable pipelines for various genomics applications, including RNA sequencing, chromatin immunoprecipitation sequencing, DNA sequencing, methylation sequencing, Hi-C, capture Hi-C, metagenomics, and Pacific Biosciences long-read assembly. The software is available under a GPLv3 open source license and is continuously updated to follow recent advances in genomics and bioinformatics. The framework has already been configured on several servers, and a Docker image is also available to facilitate additional installations.FINDINGSHere we present GenPipes, a flexible Python-based framework that facilitates the development and deployment of multi-step workflows optimized for high-performance computing clusters and the cloud. GenPipes already implements 12 validated and scalable pipelines for various genomics applications, including RNA sequencing, chromatin immunoprecipitation sequencing, DNA sequencing, methylation sequencing, Hi-C, capture Hi-C, metagenomics, and Pacific Biosciences long-read assembly. The software is available under a GPLv3 open source license and is continuously updated to follow recent advances in genomics and bioinformatics. The framework has already been configured on several servers, and a Docker image is also available to facilitate additional installations.GenPipes offers genomics researchers a simple method to analyze different types of data, customizable to their needs and resources, as well as the flexibility to create their own workflows.CONCLUSIONSGenPipes offers genomics researchers a simple method to analyze different types of data, customizable to their needs and resources, as well as the flexibility to create their own workflows.
NRC publication: Yes
Author Leveque, Gary
Bujold, David
Bourque, Guillaume
Caron, Bryan
Fillon, Joel
Caron, Maxime
Marquis, Pascale
Sandoval, Johanna
Mercier, Eloi
Tremblay, Julien
Bourgey, Mathieu
Lefebvre, Francois
Henrion, Edouard
Van, Patrick Tran
Shao, Xiaojian
Anderson de Lima Morais, David
Eveleigh, Robert
Michaud, Marc
Letourneau, Louis
Chen, Kuang Chung
Dali, Rola
Gonzalez, Emmanuel
Quirion, Pierre-Olivier
AuthorAffiliation 7 Department of Ecology and Evolution, University of Lausanne, Lausanne, Switzerland
2 McGill University and Genome Québec Innovation Center, Montréal, QC, Canada
6 Beaulieu-Saucier Université de Montréal Pharmacogenomics Centre, Montréal, QC, Canada
4 Calcul Québec, QC, Canada
9 Energy, Mining and Environment, National Research Council Canada, Montréal, QC, Canada
5 Department of Human Genetics, McGill University, Montréal, QC, Canada
1 Canadian Centre for Computational Genomics, Montréal, QC, Canada
3 McGill HPC Centre, McGill University, Montréal, QC, Canada
8 Centre de Calcul Scientifique (CCS), Université de Sherbrooke, Sherbrooke, QC, Canada
AuthorAffiliation_xml – name: 3 McGill HPC Centre, McGill University, Montréal, QC, Canada
– name: 6 Beaulieu-Saucier Université de Montréal Pharmacogenomics Centre, Montréal, QC, Canada
– name: 2 McGill University and Genome Québec Innovation Center, Montréal, QC, Canada
– name: 7 Department of Ecology and Evolution, University of Lausanne, Lausanne, Switzerland
– name: 1 Canadian Centre for Computational Genomics, Montréal, QC, Canada
– name: 8 Centre de Calcul Scientifique (CCS), Université de Sherbrooke, Sherbrooke, QC, Canada
– name: 5 Department of Human Genetics, McGill University, Montréal, QC, Canada
– name: 4 Calcul Québec, QC, Canada
– name: 9 Energy, Mining and Environment, National Research Council Canada, Montréal, QC, Canada
Author_xml – sequence: 1
  fullname: Bourgey, Mathieu
– sequence: 2
  fullname: Dali, Rola
– sequence: 3
  fullname: Eveleigh, Robert
– sequence: 4
  fullname: Chen, Kuang Chung
– sequence: 5
  fullname: Letourneau, Louis
– sequence: 6
  fullname: Fillon, Joel
– sequence: 7
  fullname: Michaud, Marc
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  fullname: Caron, Maxime
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  fullname: Sandoval, Johanna
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  fullname: Leveque, Gary
– sequence: 12
  fullname: Mercier, Eloi
– sequence: 13
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– sequence: 15
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  fullname: Shao, Xiaojian
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  fullname: Henrion, Edouard
– sequence: 20
  fullname: Gonzalez, Emmanuel
– sequence: 21
  fullname: Quirion, Pierre-Olivier
– sequence: 22
  fullname: Caron, Bryan
– sequence: 23
  fullname: Bourque, Guillaume
BackLink https://www.ncbi.nlm.nih.gov/pubmed/31185495$$D View this record in MEDLINE/PubMed
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The Author(s) 2019. Published by Oxford University Press. 2019
The Author(s) 2019. Published by Oxford University Press.
The Author(s) 2019. Published by Oxford University Press. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
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– notice: The Author(s) 2019. Published by Oxford University Press. 2019
– notice: The Author(s) 2019. Published by Oxford University Press.
– notice: The Author(s) 2019. Published by Oxford University Press. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
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IsDoiOpenAccess true
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Issue 6
Keywords workflow management systems
pipeline
genomics
workflow
frameworks
bioinformatics
Language English
License This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
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The Author(s) 2019. Published by Oxford University Press.
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Abstract Background With the decreasing cost of sequencing and the rapid developments in genomics technologies and protocols, the need for validated...
With the decreasing cost of sequencing and the rapid developments in genomics technologies and protocols, the need for validated bioinformatics software that...
Background With the decreasing cost of sequencing and the rapid developments in genomics technologies and protocols, the need for validated bioinformatics...
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SubjectTerms Bioinformatics
Chromatin
Cost analysis
Data processing
DNA Methylation
DNA sequencing
Epigenomics - methods
frameworks
Gene sequencing
Genomic analysis
Genomics
Genomics - methods
Humans
Immunoprecipitation
Metagenomics
Metagenomics - methods
Open source software
pipeline
Pipelining (computers)
Sequence Analysis, DNA - methods
Sequence Analysis, RNA - methods
Software
Technical Note
workflow
workflow management systems
Title GenPipes: an open-source framework for distributed and scalable genomic analyses
URI https://nrc-publications.canada.ca/eng/view/object/?id=2a5d6e87-1cb0-4ffd-a707-236203ca8570
https://www.ncbi.nlm.nih.gov/pubmed/31185495
https://www.proquest.com/docview/2715807352
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https://www.proquest.com/docview/2242818065
https://pubmed.ncbi.nlm.nih.gov/PMC6559338
Volume 8
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