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The rare and undiagnosed diseases diagnostic service – application of massively parallel sequencing in a state-wide clinical service
BACKGROUND: The Rare and Undiagnosed Diseases Diagnostic Service (RUDDS) refers to a genomic diagnostic platform operating within the Western Australian Government clinical services delivered through Genetic Services of Western Australia (GSWA). GSWA has provided a state-wide service for clinical ge...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4902909/ https://www.ncbi.nlm.nih.gov/pubmed/27287197 http://dx.doi.org/10.1186/s13023-016-0462-7 |
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author | Baynam, Gareth Pachter, Nicholas McKenzie, Fiona Townshend, Sharon Slee, Jennie Kiraly-Borri, Cathy Vasudevan, Anand Hawkins, Anne Broley, Stephanie Schofield, Lyn Verhoef, Hedwig Walker, Caroline E. Molster, Caron Blackwell, Jenefer M. Jamieson, Sarra Tang, Dave Lassmann, Timo Mina, Kym Beilby, John Davis, Mark Laing, Nigel Murphy, Lesley Weeramanthri, Tarun Dawkins, Hugh Goldblatt, Jack |
author_facet | Baynam, Gareth Pachter, Nicholas McKenzie, Fiona Townshend, Sharon Slee, Jennie Kiraly-Borri, Cathy Vasudevan, Anand Hawkins, Anne Broley, Stephanie Schofield, Lyn Verhoef, Hedwig Walker, Caroline E. Molster, Caron Blackwell, Jenefer M. Jamieson, Sarra Tang, Dave Lassmann, Timo Mina, Kym Beilby, John Davis, Mark Laing, Nigel Murphy, Lesley Weeramanthri, Tarun Dawkins, Hugh Goldblatt, Jack |
author_sort | Baynam, Gareth |
collection | PubMed |
description | BACKGROUND: The Rare and Undiagnosed Diseases Diagnostic Service (RUDDS) refers to a genomic diagnostic platform operating within the Western Australian Government clinical services delivered through Genetic Services of Western Australia (GSWA). GSWA has provided a state-wide service for clinical genetic care for 28 years and it serves a population of 2.5 million people across a geographical area of 2.5milion Km(2). Within this context, GSWA has established a clinically integrated genomic diagnostic platform in partnership with other public health system managers and service providers, including but not limited to the Office of Population Health Genomics, Diagnostic Genomics (PathWest Laboratories) and with executive level support from the Department of Health. Herein we describe report presents the components of this service that are most relevant to the heterogeneity of paediatric clinical genetic care. RESULTS: Briefly the platform : i) offers multiple options including non-genetic testing; monogenic and genomic (targeted in silico filtered and whole exome) analysis; and matchmaking; ii) is delivered in a patient-centric manner that is resonant with the patient journey, it has multiple points for entry, exit and re-entry to allow people access to information they can use, when they want to receive it; iii) is synchronous with precision phenotyping methods; iv) captures new knowledge, including multiple expert review; v) is integrated with current translational genomic research activities and best practice; and vi) is designed for flexibility for interactive generation of, and integration with, clinical research for diagnostics, community engagement, policy and models of care. CONCLUSION: The RUDDS has been established as part of routine clinical genetic services and is thus sustainable, equitably managed and seeks to translate new knowledge into efficient diagnostics and improved health for the whole community. |
format | Online Article Text |
id | pubmed-4902909 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49029092016-06-12 The rare and undiagnosed diseases diagnostic service – application of massively parallel sequencing in a state-wide clinical service Baynam, Gareth Pachter, Nicholas McKenzie, Fiona Townshend, Sharon Slee, Jennie Kiraly-Borri, Cathy Vasudevan, Anand Hawkins, Anne Broley, Stephanie Schofield, Lyn Verhoef, Hedwig Walker, Caroline E. Molster, Caron Blackwell, Jenefer M. Jamieson, Sarra Tang, Dave Lassmann, Timo Mina, Kym Beilby, John Davis, Mark Laing, Nigel Murphy, Lesley Weeramanthri, Tarun Dawkins, Hugh Goldblatt, Jack Orphanet J Rare Dis Research BACKGROUND: The Rare and Undiagnosed Diseases Diagnostic Service (RUDDS) refers to a genomic diagnostic platform operating within the Western Australian Government clinical services delivered through Genetic Services of Western Australia (GSWA). GSWA has provided a state-wide service for clinical genetic care for 28 years and it serves a population of 2.5 million people across a geographical area of 2.5milion Km(2). Within this context, GSWA has established a clinically integrated genomic diagnostic platform in partnership with other public health system managers and service providers, including but not limited to the Office of Population Health Genomics, Diagnostic Genomics (PathWest Laboratories) and with executive level support from the Department of Health. Herein we describe report presents the components of this service that are most relevant to the heterogeneity of paediatric clinical genetic care. RESULTS: Briefly the platform : i) offers multiple options including non-genetic testing; monogenic and genomic (targeted in silico filtered and whole exome) analysis; and matchmaking; ii) is delivered in a patient-centric manner that is resonant with the patient journey, it has multiple points for entry, exit and re-entry to allow people access to information they can use, when they want to receive it; iii) is synchronous with precision phenotyping methods; iv) captures new knowledge, including multiple expert review; v) is integrated with current translational genomic research activities and best practice; and vi) is designed for flexibility for interactive generation of, and integration with, clinical research for diagnostics, community engagement, policy and models of care. CONCLUSION: The RUDDS has been established as part of routine clinical genetic services and is thus sustainable, equitably managed and seeks to translate new knowledge into efficient diagnostics and improved health for the whole community. BioMed Central 2016-06-11 /pmc/articles/PMC4902909/ /pubmed/27287197 http://dx.doi.org/10.1186/s13023-016-0462-7 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Baynam, Gareth Pachter, Nicholas McKenzie, Fiona Townshend, Sharon Slee, Jennie Kiraly-Borri, Cathy Vasudevan, Anand Hawkins, Anne Broley, Stephanie Schofield, Lyn Verhoef, Hedwig Walker, Caroline E. Molster, Caron Blackwell, Jenefer M. Jamieson, Sarra Tang, Dave Lassmann, Timo Mina, Kym Beilby, John Davis, Mark Laing, Nigel Murphy, Lesley Weeramanthri, Tarun Dawkins, Hugh Goldblatt, Jack The rare and undiagnosed diseases diagnostic service – application of massively parallel sequencing in a state-wide clinical service |
title | The rare and undiagnosed diseases diagnostic service – application of massively parallel sequencing in a state-wide clinical service |
title_full | The rare and undiagnosed diseases diagnostic service – application of massively parallel sequencing in a state-wide clinical service |
title_fullStr | The rare and undiagnosed diseases diagnostic service – application of massively parallel sequencing in a state-wide clinical service |
title_full_unstemmed | The rare and undiagnosed diseases diagnostic service – application of massively parallel sequencing in a state-wide clinical service |
title_short | The rare and undiagnosed diseases diagnostic service – application of massively parallel sequencing in a state-wide clinical service |
title_sort | rare and undiagnosed diseases diagnostic service – application of massively parallel sequencing in a state-wide clinical service |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4902909/ https://www.ncbi.nlm.nih.gov/pubmed/27287197 http://dx.doi.org/10.1186/s13023-016-0462-7 |
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