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The Italian National External Quality Assessment Program in Molecular Genetic Testing: Results of the VII Round (2010-2011)
Since 2001 the Istituto Superiore di Sanità established a quality assurance programme for molecular genetic testing that covers four pathologies: Cystic Fibrosis (CF), Beta Thalassemia (BT), Fragile X Syndrome (FX), and Familial Adenomatous Polyposis Coli (APC). Since 2009 this activity is an instit...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3581119/ https://www.ncbi.nlm.nih.gov/pubmed/23484150 http://dx.doi.org/10.1155/2013/739010 |
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author | Censi, F. Tosto, F. Floridia, G. Marra, M. Salvatore, M. Baffico, A. M. Grasso, M. Melis, M. A. Pelo, E. Radice, P. Ravani, A. Rosatelli, C. Resta, N. Russo, S. Seia, M. Varesco, L. Falbo, V. Taruscio, D. |
author_facet | Censi, F. Tosto, F. Floridia, G. Marra, M. Salvatore, M. Baffico, A. M. Grasso, M. Melis, M. A. Pelo, E. Radice, P. Ravani, A. Rosatelli, C. Resta, N. Russo, S. Seia, M. Varesco, L. Falbo, V. Taruscio, D. |
author_sort | Censi, F. |
collection | PubMed |
description | Since 2001 the Istituto Superiore di Sanità established a quality assurance programme for molecular genetic testing that covers four pathologies: Cystic Fibrosis (CF), Beta Thalassemia (BT), Fragile X Syndrome (FX), and Familial Adenomatous Polyposis Coli (APC). Since 2009 this activity is an institutional activity and participation is open to both public and private laboratories. Seven rounds have been performed until now and the eighth is in progress. Laboratories receive 4 DNA samples with mock clinical indications. They analyze the samples using their routine procedures. A panel of assessors review the raw data and the reports; all data are managed through a web utility. In 2010 the number of participants was 43, 17, 15, 5 for CF, BT, FX, APC schemes respectively. Genotyping results were correct in 96%, 98.5%, 100%, and 100% of CF, BT, FX, and APC samples, respectively. Interpretation was correct in 74%, 91%, 88%, and 60% of CF, BT, FX, and APC reports, respectively; however in most of them it was not complete but a referral to genetic counseling was given. Reports were satisfactory in more than 60% of samples in all schemes. This work presents the 2010 results in detail comparing our data with those from other European schemes. |
format | Online Article Text |
id | pubmed-3581119 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-35811192013-03-12 The Italian National External Quality Assessment Program in Molecular Genetic Testing: Results of the VII Round (2010-2011) Censi, F. Tosto, F. Floridia, G. Marra, M. Salvatore, M. Baffico, A. M. Grasso, M. Melis, M. A. Pelo, E. Radice, P. Ravani, A. Rosatelli, C. Resta, N. Russo, S. Seia, M. Varesco, L. Falbo, V. Taruscio, D. Biomed Res Int Research Article Since 2001 the Istituto Superiore di Sanità established a quality assurance programme for molecular genetic testing that covers four pathologies: Cystic Fibrosis (CF), Beta Thalassemia (BT), Fragile X Syndrome (FX), and Familial Adenomatous Polyposis Coli (APC). Since 2009 this activity is an institutional activity and participation is open to both public and private laboratories. Seven rounds have been performed until now and the eighth is in progress. Laboratories receive 4 DNA samples with mock clinical indications. They analyze the samples using their routine procedures. A panel of assessors review the raw data and the reports; all data are managed through a web utility. In 2010 the number of participants was 43, 17, 15, 5 for CF, BT, FX, APC schemes respectively. Genotyping results were correct in 96%, 98.5%, 100%, and 100% of CF, BT, FX, and APC samples, respectively. Interpretation was correct in 74%, 91%, 88%, and 60% of CF, BT, FX, and APC reports, respectively; however in most of them it was not complete but a referral to genetic counseling was given. Reports were satisfactory in more than 60% of samples in all schemes. This work presents the 2010 results in detail comparing our data with those from other European schemes. Hindawi Publishing Corporation 2013 2013-01-29 /pmc/articles/PMC3581119/ /pubmed/23484150 http://dx.doi.org/10.1155/2013/739010 Text en Copyright © 2013 F. Censi et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Censi, F. Tosto, F. Floridia, G. Marra, M. Salvatore, M. Baffico, A. M. Grasso, M. Melis, M. A. Pelo, E. Radice, P. Ravani, A. Rosatelli, C. Resta, N. Russo, S. Seia, M. Varesco, L. Falbo, V. Taruscio, D. The Italian National External Quality Assessment Program in Molecular Genetic Testing: Results of the VII Round (2010-2011) |
title | The Italian National External Quality Assessment Program in Molecular Genetic Testing: Results of the VII Round (2010-2011) |
title_full | The Italian National External Quality Assessment Program in Molecular Genetic Testing: Results of the VII Round (2010-2011) |
title_fullStr | The Italian National External Quality Assessment Program in Molecular Genetic Testing: Results of the VII Round (2010-2011) |
title_full_unstemmed | The Italian National External Quality Assessment Program in Molecular Genetic Testing: Results of the VII Round (2010-2011) |
title_short | The Italian National External Quality Assessment Program in Molecular Genetic Testing: Results of the VII Round (2010-2011) |
title_sort | italian national external quality assessment program in molecular genetic testing: results of the vii round (2010-2011) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3581119/ https://www.ncbi.nlm.nih.gov/pubmed/23484150 http://dx.doi.org/10.1155/2013/739010 |
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