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Robustness of Next Generation Sequencing on Older Formalin-Fixed Paraffin-Embedded Tissue

Next Generation Sequencing (NGS) technologies are used to detect somatic mutations in tumors and study germ line variation. Most NGS studies use DNA isolated from whole blood or fresh frozen tissue. However, formalin-fixed paraffin-embedded (FFPE) tissues are one of the most widely available clinica...

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Autores principales: Carrick, Danielle Mercatante, Mehaffey, Michele G., Sachs, Michael C., Altekruse, Sean, Camalier, Corinne, Chuaqui, Rodrigo, Cozen, Wendy, Das, Biswajit, Hernandez, Brenda Y., Lih, Chih-Jian, Lynch, Charles F., Makhlouf, Hala, McGregor, Paul, McShane, Lisa M., Phillips Rohan, JoyAnn, Walsh, William D., Williams, Paul M., Gillanders, Elizabeth M., Mechanic, Leah E., Schully, Sheri D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4519244/
https://www.ncbi.nlm.nih.gov/pubmed/26222067
http://dx.doi.org/10.1371/journal.pone.0127353
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author Carrick, Danielle Mercatante
Mehaffey, Michele G.
Sachs, Michael C.
Altekruse, Sean
Camalier, Corinne
Chuaqui, Rodrigo
Cozen, Wendy
Das, Biswajit
Hernandez, Brenda Y.
Lih, Chih-Jian
Lynch, Charles F.
Makhlouf, Hala
McGregor, Paul
McShane, Lisa M.
Phillips Rohan, JoyAnn
Walsh, William D.
Williams, Paul M.
Gillanders, Elizabeth M.
Mechanic, Leah E.
Schully, Sheri D.
author_facet Carrick, Danielle Mercatante
Mehaffey, Michele G.
Sachs, Michael C.
Altekruse, Sean
Camalier, Corinne
Chuaqui, Rodrigo
Cozen, Wendy
Das, Biswajit
Hernandez, Brenda Y.
Lih, Chih-Jian
Lynch, Charles F.
Makhlouf, Hala
McGregor, Paul
McShane, Lisa M.
Phillips Rohan, JoyAnn
Walsh, William D.
Williams, Paul M.
Gillanders, Elizabeth M.
Mechanic, Leah E.
Schully, Sheri D.
author_sort Carrick, Danielle Mercatante
collection PubMed
description Next Generation Sequencing (NGS) technologies are used to detect somatic mutations in tumors and study germ line variation. Most NGS studies use DNA isolated from whole blood or fresh frozen tissue. However, formalin-fixed paraffin-embedded (FFPE) tissues are one of the most widely available clinical specimens. Their potential utility as a source of DNA for NGS would greatly enhance population-based cancer studies. While preliminary studies suggest FFPE tissue may be used for NGS, the feasibility of using archived FFPE specimens in population based studies and the effect of storage time on these specimens needs to be determined. We conducted a study to determine whether DNA in archived FFPE high-grade ovarian serous adenocarcinomas from Surveillance, Epidemiology and End Results (SEER) registries Residual Tissue Repositories (RTR) was present in sufficient quantity and quality for NGS assays. Fifty-nine FFPE tissues, stored from 3 to 32 years, were obtained from three SEER RTR sites. DNA was extracted, quantified, quality assessed, and subjected to whole exome sequencing (WES). Following DNA extraction, 58 of 59 specimens (98%) yielded DNA and moved on to the library generation step followed by WES. Specimens stored for longer periods of time had significantly lower coverage of the target region (6% lower per 10 years, 95% CI: 3-10%) and lower average read depth (40x lower per 10 years, 95% CI: 18-60), although sufficient quality and quantity of WES data was obtained for data mining. Overall, 90% (53/59) of specimens provided usable NGS data regardless of storage time. This feasibility study demonstrates FFPE specimens acquired from SEER registries after varying lengths of storage time and under varying storage conditions are a promising source of DNA for NGS.
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spelling pubmed-45192442015-07-31 Robustness of Next Generation Sequencing on Older Formalin-Fixed Paraffin-Embedded Tissue Carrick, Danielle Mercatante Mehaffey, Michele G. Sachs, Michael C. Altekruse, Sean Camalier, Corinne Chuaqui, Rodrigo Cozen, Wendy Das, Biswajit Hernandez, Brenda Y. Lih, Chih-Jian Lynch, Charles F. Makhlouf, Hala McGregor, Paul McShane, Lisa M. Phillips Rohan, JoyAnn Walsh, William D. Williams, Paul M. Gillanders, Elizabeth M. Mechanic, Leah E. Schully, Sheri D. PLoS One Research Article Next Generation Sequencing (NGS) technologies are used to detect somatic mutations in tumors and study germ line variation. Most NGS studies use DNA isolated from whole blood or fresh frozen tissue. However, formalin-fixed paraffin-embedded (FFPE) tissues are one of the most widely available clinical specimens. Their potential utility as a source of DNA for NGS would greatly enhance population-based cancer studies. While preliminary studies suggest FFPE tissue may be used for NGS, the feasibility of using archived FFPE specimens in population based studies and the effect of storage time on these specimens needs to be determined. We conducted a study to determine whether DNA in archived FFPE high-grade ovarian serous adenocarcinomas from Surveillance, Epidemiology and End Results (SEER) registries Residual Tissue Repositories (RTR) was present in sufficient quantity and quality for NGS assays. Fifty-nine FFPE tissues, stored from 3 to 32 years, were obtained from three SEER RTR sites. DNA was extracted, quantified, quality assessed, and subjected to whole exome sequencing (WES). Following DNA extraction, 58 of 59 specimens (98%) yielded DNA and moved on to the library generation step followed by WES. Specimens stored for longer periods of time had significantly lower coverage of the target region (6% lower per 10 years, 95% CI: 3-10%) and lower average read depth (40x lower per 10 years, 95% CI: 18-60), although sufficient quality and quantity of WES data was obtained for data mining. Overall, 90% (53/59) of specimens provided usable NGS data regardless of storage time. This feasibility study demonstrates FFPE specimens acquired from SEER registries after varying lengths of storage time and under varying storage conditions are a promising source of DNA for NGS. Public Library of Science 2015-07-29 /pmc/articles/PMC4519244/ /pubmed/26222067 http://dx.doi.org/10.1371/journal.pone.0127353 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Carrick, Danielle Mercatante
Mehaffey, Michele G.
Sachs, Michael C.
Altekruse, Sean
Camalier, Corinne
Chuaqui, Rodrigo
Cozen, Wendy
Das, Biswajit
Hernandez, Brenda Y.
Lih, Chih-Jian
Lynch, Charles F.
Makhlouf, Hala
McGregor, Paul
McShane, Lisa M.
Phillips Rohan, JoyAnn
Walsh, William D.
Williams, Paul M.
Gillanders, Elizabeth M.
Mechanic, Leah E.
Schully, Sheri D.
Robustness of Next Generation Sequencing on Older Formalin-Fixed Paraffin-Embedded Tissue
title Robustness of Next Generation Sequencing on Older Formalin-Fixed Paraffin-Embedded Tissue
title_full Robustness of Next Generation Sequencing on Older Formalin-Fixed Paraffin-Embedded Tissue
title_fullStr Robustness of Next Generation Sequencing on Older Formalin-Fixed Paraffin-Embedded Tissue
title_full_unstemmed Robustness of Next Generation Sequencing on Older Formalin-Fixed Paraffin-Embedded Tissue
title_short Robustness of Next Generation Sequencing on Older Formalin-Fixed Paraffin-Embedded Tissue
title_sort robustness of next generation sequencing on older formalin-fixed paraffin-embedded tissue
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4519244/
https://www.ncbi.nlm.nih.gov/pubmed/26222067
http://dx.doi.org/10.1371/journal.pone.0127353
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