Arteria: An automation system for a sequencing core facility

Abstract Background In recent years, nucleotide sequencing has become increasingly instrumental in both research and clinical settings. This has led to an explosive growth in sequencing data produced worldwide. As the amount of data increases, so does the need for automated solutions for data proces...

Full description

Saved in:
Bibliographic Details
Published in:Gigascience Vol. 8; no. 12
Main Authors: Dahlberg, Johan, Hermansson, Johan, Sturlaugsson, Steinar, Lysenkova, Mariya, Smeds, Patrik, Ladenvall, Claes, Guimera, Roman Valls, Reisinger, Florian, Hofmann, Oliver, Larsson, Pontus
Format: Journal Article
Language:English
Published: United States Oxford University Press 01.12.2019
Subjects:
ISSN:2047-217X, 2047-217X
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Abstract Abstract Background In recent years, nucleotide sequencing has become increasingly instrumental in both research and clinical settings. This has led to an explosive growth in sequencing data produced worldwide. As the amount of data increases, so does the need for automated solutions for data processing and analysis. The concept of workflows has gained favour in the bioinformatics community, but there is little in the scientific literature describing end-to-end automation systems. Arteria is an automation system that aims at providing a solution to the data-related operational challenges that face sequencing core facilities. Findings Arteria is built on existing open source technologies, with a modular design allowing for a community-driven effort to create plug-and-play micro-services. In this article we describe the system, elaborate on the underlying conceptual framework, and present an example implementation. Arteria can be reduced to 3 conceptual levels: orchestration (using an event-based model of automation), process (the steps involved in processing sequencing data, modelled as workflows), and execution (using a series of RESTful micro-services). This creates a system that is both flexible and scalable. Arteria-based systems have been successfully deployed at 3 sequencing core facilities. The Arteria Project code, written largely in Python, is available as open source software, and more information can be found at https://arteria-project.github.io/ . Conclusions We describe the Arteria system and the underlying conceptual framework, demonstrating how this model can be used to automate data handling and analysis in the context of a sequencing core facility.
AbstractList Background In recent years, nucleotide sequencing has become increasingly instrumental in both research and clinical settings. This has led to an explosive growth in sequencing data produced worldwide. As the amount of data increases, so does the need for automated solutions for data processing and analysis. The concept of workflows has gained favour in the bioinformatics community, but there is little in the scientific literature describing end-to-end automation systems. Arteria is an automation system that aims at providing a solution to the data-related operational challenges that face sequencing core facilities. Findings Arteria is built on existing open source technologies, with a modular design allowing for a community-driven effort to create plug-and-play micro-services. In this article we describe the system, elaborate on the underlying conceptual framework, and present an example implementation. Arteria can be reduced to 3 conceptual levels: orchestration (using an event-based model of automation), process (the steps involved in processing sequencing data, modelled as workflows), and execution (using a series of RESTful micro-services). This creates a system that is both flexible and scalable. Arteria-based systems have been successfully deployed at 3 sequencing core facilities. The Arteria Project code, written largely in Python, is available as open source software, and more information can be found at https://arteria-project.github.io/ . Conclusions We describe the Arteria system and the underlying conceptual framework, demonstrating how this model can be used to automate data handling and analysis in the context of a sequencing core facility.
In recent years, nucleotide sequencing has become increasingly instrumental in both research and clinical settings. This has led to an explosive growth in sequencing data produced worldwide. As the amount of data increases, so does the need for automated solutions for data processing and analysis. The concept of workflows has gained favour in the bioinformatics community, but there is little in the scientific literature describing end-to-end automation systems. Arteria is an automation system that aims at providing a solution to the data-related operational challenges that face sequencing core facilities. Arteria is built on existing open source technologies, with a modular design allowing for a community-driven effort to create plug-and-play micro-services. In this article we describe the system, elaborate on the underlying conceptual framework, and present an example implementation. Arteria can be reduced to 3 conceptual levels: orchestration (using an event-based model of automation), process (the steps involved in processing sequencing data, modelled as workflows), and execution (using a series of RESTful micro-services). This creates a system that is both flexible and scalable. Arteria-based systems have been successfully deployed at 3 sequencing core facilities. The Arteria Project code, written largely in Python, is available as open source software, and more information can be found at https://arteria-project.github.io/ . We describe the Arteria system and the underlying conceptual framework, demonstrating how this model can be used to automate data handling and analysis in the context of a sequencing core facility.
Abstract Background In recent years, nucleotide sequencing has become increasingly instrumental in both research and clinical settings. This has led to an explosive growth in sequencing data produced worldwide. As the amount of data increases, so does the need for automated solutions for data processing and analysis. The concept of workflows has gained favour in the bioinformatics community, but there is little in the scientific literature describing end-to-end automation systems. Arteria is an automation system that aims at providing a solution to the data-related operational challenges that face sequencing core facilities. Findings Arteria is built on existing open source technologies, with a modular design allowing for a community-driven effort to create plug-and-play micro-services. In this article we describe the system, elaborate on the underlying conceptual framework, and present an example implementation. Arteria can be reduced to 3 conceptual levels: orchestration (using an event-based model of automation), process (the steps involved in processing sequencing data, modelled as workflows), and execution (using a series of RESTful micro-services). This creates a system that is both flexible and scalable. Arteria-based systems have been successfully deployed at 3 sequencing core facilities. The Arteria Project code, written largely in Python, is available as open source software, and more information can be found at https://arteria-project.github.io/ . Conclusions We describe the Arteria system and the underlying conceptual framework, demonstrating how this model can be used to automate data handling and analysis in the context of a sequencing core facility.
Background: In recent years, nucleotide sequencing has become increasingly instrumental in both research and clinical settings. This has led to an explosive growth in sequencing data produced worldwide. As the amount of data increases, so does the need for automated solutions for data processing and analysis. The concept of workflows has gained favour in the bioinformatics community, but there is little in the scientific literature describing end-to-end automation systems. Arteria is an automation system that aims at providing a solution to the data-related operational challenges that face sequencing core facilities. Findings: Arteria is built on existing open source technologies, with a modular design allowing for a community-driven effort to create plug-and-play micro-services. In this article we describe the system, elaborate on the underlying conceptual framework, and present an example implementation. Arteria can be reduced to 3 conceptual levels: orchestration (using an event-based model of automation), process (the steps involved in processing sequencing data, modelled as workflows), and execution (using a series of RESTful micro-services). This creates a system that is both flexible and scalable. Arteria-based systems have been successfully deployed at 3 sequencing core facilities. The Arteria Project code, written largely in Python, is available as open source software, and more information can be found at https://arteria-project.github.io/. Conclusions: We describe the Arteria system and the underlying conceptual framework, demonstrating how this model can be used to automate data handling and analysis in the context of a sequencing core facility.
In recent years, nucleotide sequencing has become increasingly instrumental in both research and clinical settings. This has led to an explosive growth in sequencing data produced worldwide. As the amount of data increases, so does the need for automated solutions for data processing and analysis. The concept of workflows has gained favour in the bioinformatics community, but there is little in the scientific literature describing end-to-end automation systems. Arteria is an automation system that aims at providing a solution to the data-related operational challenges that face sequencing core facilities.BACKGROUNDIn recent years, nucleotide sequencing has become increasingly instrumental in both research and clinical settings. This has led to an explosive growth in sequencing data produced worldwide. As the amount of data increases, so does the need for automated solutions for data processing and analysis. The concept of workflows has gained favour in the bioinformatics community, but there is little in the scientific literature describing end-to-end automation systems. Arteria is an automation system that aims at providing a solution to the data-related operational challenges that face sequencing core facilities.Arteria is built on existing open source technologies, with a modular design allowing for a community-driven effort to create plug-and-play micro-services. In this article we describe the system, elaborate on the underlying conceptual framework, and present an example implementation. Arteria can be reduced to 3 conceptual levels: orchestration (using an event-based model of automation), process (the steps involved in processing sequencing data, modelled as workflows), and execution (using a series of RESTful micro-services). This creates a system that is both flexible and scalable. Arteria-based systems have been successfully deployed at 3 sequencing core facilities. The Arteria Project code, written largely in Python, is available as open source software, and more information can be found at https://arteria-project.github.io/ .FINDINGSArteria is built on existing open source technologies, with a modular design allowing for a community-driven effort to create plug-and-play micro-services. In this article we describe the system, elaborate on the underlying conceptual framework, and present an example implementation. Arteria can be reduced to 3 conceptual levels: orchestration (using an event-based model of automation), process (the steps involved in processing sequencing data, modelled as workflows), and execution (using a series of RESTful micro-services). This creates a system that is both flexible and scalable. Arteria-based systems have been successfully deployed at 3 sequencing core facilities. The Arteria Project code, written largely in Python, is available as open source software, and more information can be found at https://arteria-project.github.io/ .We describe the Arteria system and the underlying conceptual framework, demonstrating how this model can be used to automate data handling and analysis in the context of a sequencing core facility.CONCLUSIONSWe describe the Arteria system and the underlying conceptual framework, demonstrating how this model can be used to automate data handling and analysis in the context of a sequencing core facility.
Author Sturlaugsson, Steinar
Hermansson, Johan
Dahlberg, Johan
Lysenkova, Mariya
Ladenvall, Claes
Smeds, Patrik
Reisinger, Florian
Hofmann, Oliver
Larsson, Pontus
Guimera, Roman Valls
AuthorAffiliation 1 Department of Medical Sciences, Molecular Medicine and Science for Life Laboratory, Uppsala University , Box 1432, BMC 751 44, Uppsala, Sweden
2 Department of Immunology, Genetics and Pathology and Science for Life Laboratory, Uppsala University , Rudbecklaboratoriet, 751 84, Uppsala, Sweden
3 University of Melbourne Center for Cancer Research, University of Melbourne , Victorian Comprehensive Cancer Centre, Level 10, UMCCR, 305 Grattan St, Melbourne VIC 3000, Australia
AuthorAffiliation_xml – name: 1 Department of Medical Sciences, Molecular Medicine and Science for Life Laboratory, Uppsala University , Box 1432, BMC 751 44, Uppsala, Sweden
– name: 2 Department of Immunology, Genetics and Pathology and Science for Life Laboratory, Uppsala University , Rudbecklaboratoriet, 751 84, Uppsala, Sweden
– name: 3 University of Melbourne Center for Cancer Research, University of Melbourne , Victorian Comprehensive Cancer Centre, Level 10, UMCCR, 305 Grattan St, Melbourne VIC 3000, Australia
Author_xml – sequence: 1
  givenname: Johan
  orcidid: 0000-0001-6962-1460
  surname: Dahlberg
  fullname: Dahlberg, Johan
  email: johan.dahlberg@medsci.uu.se
  organization: Department of Medical Sciences, Molecular Medicine and Science for Life Laboratory, Uppsala University, Box 1432, BMC 751 44, Uppsala, Sweden
– sequence: 2
  givenname: Johan
  surname: Hermansson
  fullname: Hermansson, Johan
  organization: Department of Medical Sciences, Molecular Medicine and Science for Life Laboratory, Uppsala University, Box 1432, BMC 751 44, Uppsala, Sweden
– sequence: 3
  givenname: Steinar
  surname: Sturlaugsson
  fullname: Sturlaugsson, Steinar
  organization: Department of Medical Sciences, Molecular Medicine and Science for Life Laboratory, Uppsala University, Box 1432, BMC 751 44, Uppsala, Sweden
– sequence: 4
  givenname: Mariya
  surname: Lysenkova
  fullname: Lysenkova, Mariya
  organization: Department of Medical Sciences, Molecular Medicine and Science for Life Laboratory, Uppsala University, Box 1432, BMC 751 44, Uppsala, Sweden
– sequence: 5
  givenname: Patrik
  surname: Smeds
  fullname: Smeds, Patrik
  organization: Department of Immunology, Genetics and Pathology and Science for Life Laboratory, Uppsala University, Rudbecklaboratoriet, 751 84, Uppsala, Sweden
– sequence: 6
  givenname: Claes
  orcidid: 0000-0002-7501-6598
  surname: Ladenvall
  fullname: Ladenvall, Claes
  organization: Department of Immunology, Genetics and Pathology and Science for Life Laboratory, Uppsala University, Rudbecklaboratoriet, 751 84, Uppsala, Sweden
– sequence: 7
  givenname: Roman Valls
  orcidid: 0000-0002-0034-9697
  surname: Guimera
  fullname: Guimera, Roman Valls
  organization: University of Melbourne Center for Cancer Research, University of Melbourne, Victorian Comprehensive Cancer Centre, Level 10, UMCCR, 305 Grattan St, Melbourne VIC 3000, Australia
– sequence: 8
  givenname: Florian
  surname: Reisinger
  fullname: Reisinger, Florian
  organization: University of Melbourne Center for Cancer Research, University of Melbourne, Victorian Comprehensive Cancer Centre, Level 10, UMCCR, 305 Grattan St, Melbourne VIC 3000, Australia
– sequence: 9
  givenname: Oliver
  orcidid: 0000-0002-7738-1513
  surname: Hofmann
  fullname: Hofmann, Oliver
  organization: University of Melbourne Center for Cancer Research, University of Melbourne, Victorian Comprehensive Cancer Centre, Level 10, UMCCR, 305 Grattan St, Melbourne VIC 3000, Australia
– sequence: 10
  givenname: Pontus
  orcidid: 0000-0002-8597-5565
  surname: Larsson
  fullname: Larsson, Pontus
  organization: Department of Medical Sciences, Molecular Medicine and Science for Life Laboratory, Uppsala University, Box 1432, BMC 751 44, Uppsala, Sweden
BackLink https://www.ncbi.nlm.nih.gov/pubmed/31825479$$D View this record in MEDLINE/PubMed
https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-357972$$DView record from Swedish Publication Index (Uppsala universitet)
BookMark eNqNkl1rFTEQhoNUbK39A17IgjdeuJqPzZeIcKifUPBGxbswJye7puwmp0lWOf56U7eV014Uc5OBPO87M5l5iA5CDA6hxwS_IFizl4MfIFvvgnU1_k0Yv4eOKO5kS4n8frAXH6KTnM9xPVIqJdkDdMiIoryT-gi9XqXikodXzSo0MJc4QfExNHmXi5uaPqYGmuwu5prIh6GxMbmmB-tHX3aP0P0exuxOru5j9PX9uy-nH9uzzx8-na7OWssZK61eE6H7Xiq3dlQwKwTGIHkH2MmNcBgUIaCs3LA1I5pR1jPoQHQaFHTSEnaMni---ZfbzmuzTX6CtDMRvHnrv61MTIOZZ8O41JJW_M2CV3ZyG-tCSTDeUN18Cf6HGeJPIzTmjF8aPLsySLF2nouZfLZuHCG4OGdDGe00kYLrij69hZ7HOYX6G4bVrmXHMVZ3UVQSroiow6rUk_26_xV8Pa0KqAWwKeacXG-sL3_nVdvwoyHYXO6G2dsNs-xGldJb0mv3O0XtIorz9n_4P5AL0Qs
CitedBy_id crossref_primary_10_1093_gigascience_giz135
Cites_doi 10.1038/nrg.2016.86
10.1038/nature15393
10.1038/35057062
10.1038/nature14447
10.1186/s13062-015-0071-8
10.1371/journal.pbio.1002195
10.1093/nar/gkw343
10.6084/m9.figshare.3115156.v2
10.1186/s13742-016-0132-7
10.1093/gigascience/giz135
10.1186/s13321-016-0179-6
10.1093/bioinformatics/btx817
10.1038/nrg.2016.49
10.1109/HPCSim.2014.6903742
10.5281/zenodo.1204292
ContentType Journal Article
Copyright 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.
Copyright_xml – 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.
DBID TOX
AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
JQ2
K9.
7X8
5PM
ACNBI
ADTPV
AOWAS
D8T
DF2
ZZAVC
DOI 10.1093/gigascience/giz135
DatabaseName Oxford Journals Open Access Collection
CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
ProQuest Computer Science Collection
ProQuest Health & Medical Complete (Alumni)
MEDLINE - Academic
PubMed Central (Full Participant titles)
SWEPUB Uppsala universitet full text
SwePub
SwePub Articles
SWEPUB Freely available online
SWEPUB Uppsala universitet
SwePub Articles full text
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
ProQuest Health & Medical Complete (Alumni)
ProQuest Computer Science Collection
MEDLINE - Academic
DatabaseTitleList ProQuest Health & Medical Complete (Alumni)
ProQuest Health & Medical Complete (Alumni)
MEDLINE


MEDLINE - Academic
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: TOX
  name: Oxford Journals Open Access Collection
  url: https://academic.oup.com/journals/
  sourceTypes: Publisher
– sequence: 3
  dbid: 7X8
  name: MEDLINE - Academic
  url: https://search.proquest.com/medline
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Library & Information Science
EISSN 2047-217X
ExternalDocumentID oai_DiVA_org_uu_357972
PMC6905352
31825479
10_1093_gigascience_giz135
10.1093/gigascience/giz135
Genre Research Support, Non-U.S. Gov't
Journal Article
GrantInformation_xml – fundername: Science for Life Laboratory
  funderid: 10.13039/501100009252
– fundername: National Health and Medical Research Council
  grantid: GNT1113531
  funderid: 10.13039/501100000925
– fundername: Knut and Alice Wallenberg Foundation
  funderid: 10.13039/501100004063
– fundername: National Genomics Infrastructure
– fundername: SNP&SEQ Technology Platform in Uppsala
– fundername: Australian Genomics Health Alliance
– fundername: Uppsala University Hospital
  grantid: ALF-717721
  funderid: 10.13039/501100005423
– fundername: Swedish Research Council
  funderid: 10.13039/501100004359
– fundername: ;
– fundername: ; ;
  grantid: GNT1113531
– fundername: ; ;
  grantid: ALF-717721
– fundername: ; ;
GroupedDBID -A0
0R~
3V.
4.4
53G
5VS
7X7
88E
8FE
8FG
8FH
8FI
8FJ
AAFWJ
AAHBH
AAPPN
AAPXW
AAVAP
ABDBF
ABPTD
ABUWG
ABXVV
ACGFS
ACPRK
ACRMQ
ADBBV
ADINQ
ADRAZ
ADUKV
AEGXH
AENZO
AFKRA
AFPKN
AFULF
AHBYD
AHSBF
AHYZX
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AOIJS
ARAPS
AZQEC
BAWUL
BAYMD
BBNVY
BCNDV
BENPR
BFQNJ
BGLVJ
BHPHI
BMC
BPHCQ
BTTYL
BVXVI
C24
C6C
CCPQU
DIK
DWQXO
EBS
EJD
FYUFA
GNUQQ
GROUPED_DOAJ
GX1
H13
HCIFZ
HMCUK
HYE
IAO
IHR
IHW
INH
INR
IPNFZ
ITC
K6V
K7-
KQ8
KSI
LK8
M0N
M1P
M48
M7P
M~E
O9-
OK1
P62
PIMPY
PQQKQ
PROAC
PSQYO
RBZ
RIG
RNS
ROL
ROX
RPM
RSV
SBL
SOJ
TJX
TOX
UKHRP
AAYXX
ABEJV
ABGNP
ACUHS
AMNDL
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
JQ2
K9.
7X8
5PM
88I
ACNBI
ADTPV
AFFHD
AOWAS
D8T
DF2
IGS
M2P
PHGZM
PHGZT
PJZUB
PPXIY
PQGLB
ZZAVC
ID FETCH-LOGICAL-c533t-9b169ff78ebe263c6600a754a0e7d6e0a811a8c7d3b319323f3a4a649a8a47c13
IEDL.DBID TOX
ISICitedReferencesCount 0
ISICitedReferencesURI http://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestLinkType=CitingArticles&DestApp=WOS_CPL&KeyUT=000506804600004&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
ISSN 2047-217X
IngestDate Tue Nov 04 16:54:33 EST 2025
Thu Aug 21 14:00:10 EDT 2025
Thu Oct 02 09:47:04 EDT 2025
Tue Oct 07 06:34:58 EDT 2025
Tue Oct 07 06:44:03 EDT 2025
Thu Apr 03 07:07:14 EDT 2025
Tue Nov 18 22:31:05 EST 2025
Sat Nov 29 02:21:50 EST 2025
Wed Sep 11 04:40:39 EDT 2024
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 12
Keywords automation
orchestration
workflows
sequencing
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.
http://creativecommons.org/licenses/by/4.0
The Author(s) 2019. Published by Oxford University Press.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c533t-9b169ff78ebe263c6600a754a0e7d6e0a811a8c7d3b319323f3a4a649a8a47c13
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ORCID 0000-0002-7738-1513
0000-0002-0034-9697
0000-0002-8597-5565
0000-0002-7501-6598
0000-0001-6962-1460
OpenAccessLink https://dx.doi.org/10.1093/gigascience/giz135
PMID 31825479
PQID 2715816047
PQPubID 2040230
ParticipantIDs swepub_primary_oai_DiVA_org_uu_357972
pubmedcentral_primary_oai_pubmedcentral_nih_gov_6905352
proquest_miscellaneous_2324917659
proquest_journals_3169745008
proquest_journals_2715816047
pubmed_primary_31825479
crossref_citationtrail_10_1093_gigascience_giz135
crossref_primary_10_1093_gigascience_giz135
oup_primary_10_1093_gigascience_giz135
PublicationCentury 2000
PublicationDate 2019-12-01
PublicationDateYYYYMMDD 2019-12-01
PublicationDate_xml – month: 12
  year: 2019
  text: 2019-12-01
  day: 01
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
– name: Oxford
PublicationTitle Gigascience
PublicationTitleAlternate Gigascience
PublicationYear 2019
Publisher Oxford University Press
Publisher_xml – name: Oxford University Press
References Lander (2024111714412175200_bib1) 2001; 409
2024111714412175200_bib28
Stephens (2024111714412175200_bib6) 2015; 13
Amstutz (2024111714412175200_bib11) 2016
Arteria Packs. arteria-project/arteria-packs (2024111714412175200_bib22) 2019
ISO/IEC 17025:2005 - General requirements for the competence of testing and calibration laboratories (2024111714412175200_bib20) 2014
Dahlberg (2024111714412175200_bib23) 2018
Leipzig (2024111714412175200_bib10) 2017; 18
Apache. GitHub (2024111714412175200_bib13) 2017
Ashley (2024111714412175200_bib4) 2016; 17
Lampa (2024111714412175200_bib9) 2016; 8
Chapman (2024111714412175200_bib24)
1000 Genomes Project Consortium (2024111714412175200_bib3) 2015; 526
RabbitMQ - Messaging that just works (2024111714412175200_bib16) 2018
2024111714412175200_bib26
The Arteria Project (2024111714412175200_bib17) 2019
2024111714412175200_bib21
Mistral (2024111714412175200_bib19) 2019
Goodwin (2024111714412175200_bib5) 2016; 17
Spjuth (2024111714412175200_bib8) 2015; 10
Cuccuru (2024111714412175200_bib14) 2014
Spotify. Luigi. GitHub. (2024111714412175200_bib12) 2017
Afgan (2024111714412175200_bib15) 2016; 44
Nakken (2024111714412175200_bib25) 2018; 34
Spjuth (2024111714412175200_bib7) 2016; 5
StackStorm. StackStorm/st2. GitHub (2024111714412175200_bib18) 2017
Spang (2024111714412175200_bib2) 2015; 521
References_xml – ident: 2024111714412175200_bib24
– volume: 17
  start-page: 507
  year: 2016
  ident: 2024111714412175200_bib4
  article-title: Towards precision medicine
  publication-title: Nat Rev Genet
  doi: 10.1038/nrg.2016.86
– year: 2017
  ident: 2024111714412175200_bib18
– volume: 526
  start-page: 68
  year: 2015
  ident: 2024111714412175200_bib3
  article-title: A global reference for human genetic variation
  publication-title: Nature
  doi: 10.1038/nature15393
– volume: 18
  start-page: 530
  year: 2017
  ident: 2024111714412175200_bib10
  article-title: A review of bioinformatic pipeline frameworks
  publication-title: Brief Bioinform
– year: 2019
  ident: 2024111714412175200_bib17
– year: 2018
  ident: 2024111714412175200_bib16
– volume: 409
  start-page: 860
  year: 2001
  ident: 2024111714412175200_bib1
  article-title: Initial sequencing and analysis of the human genome
  publication-title: Nature
  doi: 10.1038/35057062
– volume: 521
  start-page: 173
  year: 2015
  ident: 2024111714412175200_bib2
  article-title: Complex archaea that bridge the gap between prokaryotes and eukaryotes
  publication-title: Nature
  doi: 10.1038/nature14447
– ident: 2024111714412175200_bib26
– year: 2019
  ident: 2024111714412175200_bib22
– volume: 10
  start-page: 43
  year: 2015
  ident: 2024111714412175200_bib8
  article-title: Experiences with workflows for automating data-intensive bioinformatics
  publication-title: Biol Direct
  doi: 10.1186/s13062-015-0071-8
– year: 2014
  ident: 2024111714412175200_bib20
– volume: 13
  start-page: e1002195
  year: 2015
  ident: 2024111714412175200_bib6
  article-title: Big Data: astronomical or genomical?
  publication-title: PLoS Biol
  doi: 10.1371/journal.pbio.1002195
– volume: 44
  start-page: W3
  year: 2016
  ident: 2024111714412175200_bib15
  article-title: The Galaxy platform for accessible, reproducible and collaborative biomedical analyses: 2016 update
  publication-title: Nucleic Acids Res
  doi: 10.1093/nar/gkw343
– year: 2017
  ident: 2024111714412175200_bib12
– year: 2016
  ident: 2024111714412175200_bib11
  article-title: Common Workflow Language, v1.0
  publication-title: Figshare
  doi: 10.6084/m9.figshare.3115156.v2
– volume: 5
  start-page: 26
  year: 2016
  ident: 2024111714412175200_bib7
  article-title: Recommendations on e-infrastructures for next-generation sequencing
  publication-title: Gigascience
  doi: 10.1186/s13742-016-0132-7
– ident: 2024111714412175200_bib28
  doi: 10.1093/gigascience/giz135
– year: 2019
  ident: 2024111714412175200_bib19
– ident: 2024111714412175200_bib21
– volume: 8
  start-page: 67
  year: 2016
  ident: 2024111714412175200_bib9
  article-title: Towards agile large-scale predictive modelling in drug discovery with flow-based programming design principles
  publication-title: J Cheminform
  doi: 10.1186/s13321-016-0179-6
– volume: 34
  start-page: 1778
  issue: 10
  year: 2018
  ident: 2024111714412175200_bib25
  article-title: Personal Cancer Genome Reporter: variant interpretation report for precision oncology
  publication-title: Bioinformatics
  doi: 10.1093/bioinformatics/btx817
– year: 2017
  ident: 2024111714412175200_bib13
– volume: 17
  start-page: 333
  year: 2016
  ident: 2024111714412175200_bib5
  article-title: Coming of age: ten years of next-generation sequencing technologies
  publication-title: Nat Rev Genet
  doi: 10.1038/nrg.2016.49
– start-page: 600
  volume-title: 2014 International Conference on High Performance Computing & Simulation (HPCS), Bologna, Italy
  year: 2014
  ident: 2024111714412175200_bib14
  article-title: An automated infrastructure to support high-throughput bioinformatics
  doi: 10.1109/HPCSim.2014.6903742
– year: 2018
  ident: 2024111714412175200_bib23
  article-title: Reduced size Illumina NovaSeq runfolder
  publication-title: Zenodo
  doi: 10.5281/zenodo.1204292
SSID ssj0000778873
Score 2.1475713
Snippet Abstract Background In recent years, nucleotide sequencing has become increasingly instrumental in both research and clinical settings. This has led to an...
In recent years, nucleotide sequencing has become increasingly instrumental in both research and clinical settings. This has led to an explosive growth in...
Background In recent years, nucleotide sequencing has become increasingly instrumental in both research and clinical settings. This has led to an explosive...
Background: In recent years, nucleotide sequencing has become increasingly instrumental in both research and clinical settings. This has led to an explosive...
SourceID swepub
pubmedcentral
proquest
pubmed
crossref
oup
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
SubjectTerms Automation
Bioinformatics
Cancer research
Data analysis
Data processing
Electronic Data Processing - methods
High-Throughput Nucleotide Sequencing - methods
Human error
Humans
Infrastructure
Laboratories
Medical research
Modular design
Nucleotides
Open source software
Public domain
Python
Science
Sequences
Software
Technical Note
Workflow
Title Arteria: An automation system for a sequencing core facility
URI https://www.ncbi.nlm.nih.gov/pubmed/31825479
https://www.proquest.com/docview/2715816047
https://www.proquest.com/docview/3169745008
https://www.proquest.com/docview/2324917659
https://pubmed.ncbi.nlm.nih.gov/PMC6905352
https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-357972
Volume 8
WOSCitedRecordID wos000506804600004&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
journalDatabaseRights – providerCode: PRVADU
  databaseName: BioMed Central
  customDbUrl:
  eissn: 2047-217X
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0000778873
  issn: 2047-217X
  databaseCode: RBZ
  dateStart: 20120101
  isFulltext: true
  titleUrlDefault: https://www.biomedcentral.com/search/
  providerName: BioMedCentral
– providerCode: PRVHPJ
  databaseName: ROAD: Directory of Open Access Scholarly Resources
  customDbUrl:
  eissn: 2047-217X
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0000778873
  issn: 2047-217X
  databaseCode: M~E
  dateStart: 20120101
  isFulltext: true
  titleUrlDefault: https://road.issn.org
  providerName: ISSN International Centre
– providerCode: PRVASL
  databaseName: Oxford Journals Open Access Collection
  customDbUrl:
  eissn: 2047-217X
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0000778873
  issn: 2047-217X
  databaseCode: TOX
  dateStart: 20110101
  isFulltext: true
  titleUrlDefault: https://academic.oup.com/journals/
  providerName: Oxford University Press
link http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1La9wwEB7a0EMvfSRp6-aBAmkuxdSyZD1KLkubkFPaQxr2JsavxFC8JbsutL8-I1sxMVlKejOMxoh5aEbSzCeAQ1kmKdYyidOSV7Gs8zLOM5HGHim98IBtXGH_2IQ-Pzfzuf0emtWXa67wrfh01VxhCAf0_ZcL31LOM-Ot-uLbfDxRSbSvjBOhM2Y95yT6TDra7iWWD-sjJyiifeQ5ffmfc34FL0KKyWaDTbyGJ1W7CXuhQYEdsdCB5DXCgmtvwfHM13Y2-JnNWobdahEGDEjPjDgYslB3TdGOefRLVmPhS2v_bMOP05OLL2dxeFkhLii9W8U258of1hpSYapEoSjtQZ1JTCpdqipBwzmaQpciFz7DE7VAiUpaNCh1wcUb2GgXbfUOmEoqi37dNXUqafNhszpHk2qtPNSirSPgdxJ3RYAd969f_HTD9bdw92TlBllF8HHk-TWAbvxz9BEp8lEDd-907YKnLl2qyZS4SqReSxYkKC0zypQiOBjJ5IL-XgXbatHRLygppV2vymwEbwfLGWdDSyZtwTVR9MSmxgEe3ntKaZvrHuZb2R57J4IPg_VNWL42lzNHFue6zolMW52-f6wYduA5ZX12qMnZhY3VTVftwbPi96pZ3uzDUz03-71n3QLC0Cfd
linkProvider Oxford University Press
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Arteria%3A+An+automation+system+for+a+sequencing+core+facility&rft.jtitle=Gigascience&rft.au=Dahlberg%2C+Johan&rft.au=Hermansson%2C+Johan&rft.au=Sturlaugsson%2C+Steinar&rft.au=Lysenkova%2C+Mariya&rft.date=2019-12-01&rft.pub=Oxford+University+Press&rft.eissn=2047-217X&rft.volume=8&rft.issue=12&rft_id=info:doi/10.1093%2Fgigascience%2Fgiz135&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2047-217X&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2047-217X&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2047-217X&client=summon