scholarly journals Shared Data Science Infrastructure for Genomics Data

2019 ◽  
Author(s):  
Hamid Bagheri ◽  
Usha Muppirala ◽  
Rick Masonbrink ◽  
Andrew J Severin ◽  
Hridesh Rajan

Abstract Background: Creating a scalable computational infrastructure to analyze the wealth of information contained in data repositories is difficult due to significant barriers in organizing, extracting and analyzing relevant data. Shared data science infrastructures like Boa_g is needed to efficiently process and parse data contained in large data repositories. The main features of Boa_g are inspired from existing languages for data intensive computing and can easily integrate data from biological data repositories. Results: As a proof of concept, Boa for genomics, Boa_g, has been implemented to analyze RefSeq’s 153,848 annotation (GFF) and assembly (FASTA) file metadata. Boa_g provides a massive improvement from existing solutions like Python and MongoDB, by utilizing a domain-specific language that uses Hadoop infrastructure for a smaller storage footprint that scales well and requires fewer lines of code. We execute scripts through Boa_g to answer questions about the genomes in RefSeq. We identify the largest and smallest genomes deposited, explore exon frequencies for assemblies after 2016, identify the most commonly used bacterial genome assembly program, and address how animal genome assemblies have improved since 2016. Boa_g databases provide a significant reduction in required storage of the raw data and a significant speed up in its ability to query large datasets due to automated parallelization and distribution of Hadoop infrastructure during computations. Conclusions: In order to keep pace with our ability to produce biological data, innovative methods are required. The Shared Data Science Infrastructure, Boa_g, provides researchers a greater access to researchers to efficiently explore data in new ways. We demonstrate the potential of a the domain specific language Boa_g using the RefSeq database to explore how deposited genome assemblies and annotations are changing over time. This is a small example of how Boa_g could be used with large biological datasets.

2019 ◽  
Author(s):  
Hamid Bagheri ◽  
Usha Muppirala ◽  
Rick Masonbrink ◽  
Andrew J Severin ◽  
Hridesh Rajan

Abstract Background: Creating a scalable computational infrastructure to analyze the wealth of information contained in data repositories is difficult due to significant barriers in organizing, extracting and analyzing relevant data. Shared data science infrastructures like Boa_g is needed to efficiently process and parse data contained in large data repositories. The main features of Boa_g are inspired from existing languages for data intensive computing and can easily integrate data from biological data repositories. Results: As a proof of concept, Boa for genomics, Boa_g, has been implemented to analyze RefSeq’s 153,848 annotation (GFF) and assembly (FASTA) file metadata. Boa_g provides a massive improvement from existing solutions like Python and MongoDB, by utilizing a domain-specific language that uses Hadoop infrastructure for a smaller storage footprint that scales well and requires fewer lines of code. We execute scripts through Boa_g to answer questions about the genomes in RefSeq. We identify the largest and smallest genomes deposited, explore exon frequencies for assemblies after 2016, identify the most commonly used bacterial genome assembly program, and address how animal genome assemblies have improved since 2016. Boa_g databases provide a significant reduction in required storage of the raw data and a significant speed up in its ability to query large datasets due to automated parallelization and distribution of Hadoop infrastructure during computations. Conclusions: In order to keep pace with our ability to produce biological data, innovative methods are required. The Shared Data Science Infrastructure, Boa_g, provides researchers a greater access to researchers to efficiently explore data in new ways. We demonstrate the potential of a the domain specific language Boa_g using the RefSeq database to explore how deposited genome assemblies and annotations are changing over time. This is a small example of how Boa_g could be used with large biological datasets.


2019 ◽  
Author(s):  
Hamid Bagheri ◽  
Usha Muppirala ◽  
Rick Masonbrink ◽  
Andrew J Severin ◽  
Hridesh Rajan

Abstract Background: Creating a scalable computational infrastructure to analyze the wealth of information contained in data repositories is difficult due to significant barriers in organizing, extracting and analyzing relevant data. Shared data science infrastructures like Boa_g is needed to efficiently process and parse data contained in large data repositories. The main features of Boa_g are inspired from existing languages for data intensive computing and can easily integrate data from biological data repositories. Results: As a proof of concept, Boa for genomics, Boa_g, has been implemented to analyze RefSeq’s 153,848 annotation (GFF) and assembly (FASTA) file metadata. Boa_g provides a massive improvement from existing solutions like Python and MongoDB, by utilizing a domain-specific language that uses Hadoop infrastructure for a smaller storage footprint that scales well and requires fewer lines of code. We execute scripts through Boa_g to answer questions about the genomes in RefSeq. We identify the largest and smallest genomes deposited, explore exon frequencies for assemblies after 2016, identify the most commonly used bacterial genome assembly program, and address how animal genome assemblies have improved since 2016. Boa_g databases provide a significant reduction in required storage of the raw data and a significant speed up in its ability to query large datasets due to automated parallelization and distribution of Hadoop infrastructure during computations. Conclusions: In order to keep pace with our ability to produce biological data, innovative methods are required. The Shared Data Science Infrastructure, Boa_g, provides researchers a greater access to researchers to efficiently explore data in new ways. We demonstrate the potential of a the domain specific language Boa_g using the RefSeq database to explore how deposited genome assemblies and annotations are changing over time. This is a small example of how Boa_g could be used with large biological datasets.


2018 ◽  
Author(s):  
Hamid Bagher ◽  
Usha Muppiral ◽  
Andrew J Severin ◽  
Hridesh Rajan

AbstractBackgroundCreating a computational infrastructure to analyze the wealth of information contained in data repositories that scales well is difficult due to significant barriers in organizing, extracting and analyzing relevant data. Shared Data Science Infrastructures like Boa can be used to more efficiently process and parse data contained in large data repositories. The main features of Boa are inspired from existing languages for data intensive computing and can easily integrate data from biological data repositories.ResultsHere, we present an implementation of Boa for Genomic research (BoaG) on a relatively small data repository: RefSeq’s 97,716 annotation (GFF) and assembly (FASTA) files and metadata. We used BoaG to query the entire RefSeq dataset and gain insight into the RefSeq genome assemblies and gene model annotations and show that assembly quality using the same assembler varies depending on species.ConclusionsIn order to keep pace with our ability to produce biological data, innovative methods are required. The Shared Data Science Infrastructure, BoaG, can provide greater access to researchers to efficiently explore data in ways previously not possible for anyone but the most well funded research groups. We demonstrate the efficiency of BoaG to explore the RefSeq database of genome assemblies and annotations to identify interesting features of gene annotation as a proof of concept for much larger datasets.


Author(s):  
Jessica Ray ◽  
Ajav Brahmakshatriya ◽  
Richard Wang ◽  
Shoaib Kamil ◽  
Albert Reuther ◽  
...  

Author(s):  
Paulo Perez ◽  
Philippe Roose ◽  
Yudith Cardinale ◽  
Marc Dalmau ◽  
Dominique Masson ◽  
...  

2021 ◽  
Vol 205 ◽  
pp. 102610
Author(s):  
Davide Ancona ◽  
Luca Franceschini ◽  
Angelo Ferrando ◽  
Viviana Mascardi

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