Sensitive detection of tumor mutations from blood and its application to immunotherapy prognosis

It is possible to call single-nucleotide variant (SNV) in cell-free DNA (cfDNA), but the accuracy of detection is often affected by low tumour cfDNA content. Here, the authors develop a method, cfSNV, and show that it can be used even for medium-coverage whole exome sequencing of cfDNA.

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Autores principales: Shuo Li, Zorawar S. Noor, Weihua Zeng, Mary L. Stackpole, Xiaohui Ni, Yonggang Zhou, Zuyang Yuan, Wing Hung Wong, Vatche G. Agopian, Steven M. Dubinett, Frank Alber, Wenyuan Li, Edward B. Garon, Xianghong Jasmine Zhou
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Lenguaje:EN
Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/b75641b56a1844ef8994d8abd02e0b66
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spelling oai:doaj.org-article:b75641b56a1844ef8994d8abd02e0b662021-12-02T15:23:10ZSensitive detection of tumor mutations from blood and its application to immunotherapy prognosis10.1038/s41467-021-24457-22041-1723https://doaj.org/article/b75641b56a1844ef8994d8abd02e0b662021-07-01T00:00:00Zhttps://doi.org/10.1038/s41467-021-24457-2https://doaj.org/toc/2041-1723It is possible to call single-nucleotide variant (SNV) in cell-free DNA (cfDNA), but the accuracy of detection is often affected by low tumour cfDNA content. Here, the authors develop a method, cfSNV, and show that it can be used even for medium-coverage whole exome sequencing of cfDNA.Shuo LiZorawar S. NoorWeihua ZengMary L. StackpoleXiaohui NiYonggang ZhouZuyang YuanWing Hung WongVatche G. AgopianSteven M. DubinettFrank AlberWenyuan LiEdward B. GaronXianghong Jasmine ZhouNature PortfolioarticleScienceQENNature Communications, Vol 12, Iss 1, Pp 1-14 (2021)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Shuo Li
Zorawar S. Noor
Weihua Zeng
Mary L. Stackpole
Xiaohui Ni
Yonggang Zhou
Zuyang Yuan
Wing Hung Wong
Vatche G. Agopian
Steven M. Dubinett
Frank Alber
Wenyuan Li
Edward B. Garon
Xianghong Jasmine Zhou
Sensitive detection of tumor mutations from blood and its application to immunotherapy prognosis
description It is possible to call single-nucleotide variant (SNV) in cell-free DNA (cfDNA), but the accuracy of detection is often affected by low tumour cfDNA content. Here, the authors develop a method, cfSNV, and show that it can be used even for medium-coverage whole exome sequencing of cfDNA.
format article
author Shuo Li
Zorawar S. Noor
Weihua Zeng
Mary L. Stackpole
Xiaohui Ni
Yonggang Zhou
Zuyang Yuan
Wing Hung Wong
Vatche G. Agopian
Steven M. Dubinett
Frank Alber
Wenyuan Li
Edward B. Garon
Xianghong Jasmine Zhou
author_facet Shuo Li
Zorawar S. Noor
Weihua Zeng
Mary L. Stackpole
Xiaohui Ni
Yonggang Zhou
Zuyang Yuan
Wing Hung Wong
Vatche G. Agopian
Steven M. Dubinett
Frank Alber
Wenyuan Li
Edward B. Garon
Xianghong Jasmine Zhou
author_sort Shuo Li
title Sensitive detection of tumor mutations from blood and its application to immunotherapy prognosis
title_short Sensitive detection of tumor mutations from blood and its application to immunotherapy prognosis
title_full Sensitive detection of tumor mutations from blood and its application to immunotherapy prognosis
title_fullStr Sensitive detection of tumor mutations from blood and its application to immunotherapy prognosis
title_full_unstemmed Sensitive detection of tumor mutations from blood and its application to immunotherapy prognosis
title_sort sensitive detection of tumor mutations from blood and its application to immunotherapy prognosis
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/b75641b56a1844ef8994d8abd02e0b66
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