ARCHETYPE Sequencing assay (openEHR-EHR-CLUSTER.sequencing_assay.v0)

ARCHETYPE IDopenEHR-EHR-CLUSTER.sequencing_assay.v0
ConceptSequencing assay
DescriptionTo record details of the sequencing analysis including a list of all tested genes if panel sequencing was performed.
UseUse to record details of the performed sequencing analysis including a list of all tested genes if panel sequencing was performed. One or more instances of this archetype may be nested within the 'Testing details' SLOT in the OBSERVATION.laboratory_test_result.
MisuseUsed only to document the analysis protocol but not to document the results of the sequence analysis. The results are documented with the archetype 'genetic variant'.
PurposeTo record details of the performed sequencing analysis including a list of all tested genes if panel sequencing was performed.
References
Copyright© HiGHmed, openEHR Foundation
AuthorsNom de l'autor: Aurelie Tomczak
Organització: Institute of Pathology, University Hospital Heidelberg
Correu electrònic: au.tomczak@yahoo.com
Data d'autor original: 2019-06-24
Other Details LanguageNom de l'autor: Aurelie Tomczak
Organització: Institute of Pathology, University Hospital Heidelberg
Correu electrònic: au.tomczak@yahoo.com
Data d'autor original: 2019-06-24
OtherDetails Language Independent{licence=This work is licensed under the Creative Commons Attribution-ShareAlike 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-sa/4.0/., custodian_organisation=openEHR Foundation, original_namespace=org.openehr, original_publisher=openEHR Foundation, custodian_namespace=org.openehr, MD5-CAM-1.0.1=9B3D1743DC734C308CC6923B05E0F26B, build_uid=953ae6df-de07-4969-a3fe-5ef081772fc9, revision=0.0.1-alpha}
KeywordsSequencing, Genomics, Panel, Assay, Pathology, Sequencing analysis, Panel sequencing, Gene, Specimen
Lifecyclein_development
UID80b7cd2c-11f8-429f-80a4-5c341a5b816f
Language useden
Citeable Identifier1380.146.152
Revision Number0.0.1-alpha
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Christina Jaeger-Schmidt, Heidelberg University Hospital, Germany
Gideon Giacomelli, Charité Berlin, Germany
Florian Kaercher, Charité Berlin, Germany
Heather Leslie, Atomica Informatics, Australia (openEHR Editor)
Ian McNicoll, freshEHR Clinical Informatics, United Kingdom (openEHR Editor)
Silje Ljosland Bakke, Nasjonal IKT HF, Norway (openEHR Editor)
Francesca Frexia, CRS4 - Center for advanced studies, research and development in Sardinia, Italy
Cecilia Mascia, CRS4, Italy (openEHR Editor)
Paolo Uva, CRS4, Italy
Gianluigi Zanetti, CRS4, Italy, originalLanguage=en, translators=
  • alemany: Aurelie Tomczak, Institute of Pathology, University Hospital Heidelberg, Uniklinikum Heidelberg, au.tomczak@yahoo.com, aurelie.tomczak@med.uni-heidelberg.de
  • Bokmål noruec: Liv Laugen, Vebjørn Arntzen, ​Oslo University Hospital, Norway, liv.laugen@ous-hf.no, varntzen@ous-hf.no
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    • MLPA
    • Sanger sequencing
    • Fragment analysis
    • Methylation assay
    • Miscellaneous
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    • NGS (amplicon)
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    • Array-CGH
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    • Sanger sequencing
    • Fragment analysis
    • Methylation assay
    • Miscellaneous
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