Low-depth sequencing for copy number abnormalities in multiple myeloma supersedes fluorescent in situ hybridization in scope and resolution

Manal O. Elnenaei; Philipp Knopf; Samuel D. Cutler; Keaton Sinclair; Mohamed Abou El Hassan; Wenda Greer; Marissa Goudie; Julie Wagner; Darrell White; Stephen Couban; Nicholas Forward; Daniel Gaston; Clinton J.V. Campbell

doi:10.1111/cge.13561

Low-depth sequencing for copy number abnormalities in multiple myeloma supersedes fluorescent in situ hybridization in scope and resolution

Manal O. Elnenaei, Philipp Knopf, Samuel D. Cutler, Keaton Sinclair, Mohamed Abou El Hassan, Wenda Greer, Marissa Goudie, Julie Wagner, Darrell White, Stephen Couban, Nicholas Forward, Daniel Gaston, Clinton J.V. Campbell

Pharmacology, Toxicology and Pharmaceutics

科研成果: 期刊稿件 › 文章 › 同行评审

5 引用（Scopus）

源语言	英语
页（从-至）	163-168
页数	6
期刊	Clinical Genetics
卷	96
期	2
DOI	https://doi.org/10.1111/cge.13561
出版状态	已出版 - 8月 2019

!!!ASJC Scopus Subject Areas

遗传学
遗传学（临床）

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Elnenaei, M. O., Knopf, P., Cutler, S. D., Sinclair, K., Abou El Hassan, M., Greer, W., Goudie, M., Wagner, J., White, D., Couban, S., Forward, N., Gaston, D., & Campbell, C. J. V. (2019). Low-depth sequencing for copy number abnormalities in multiple myeloma supersedes fluorescent in situ hybridization in scope and resolution. Clinical Genetics, 96(2), 163-168. https://doi.org/10.1111/cge.13561

Elnenaei, MO, Knopf, P, Cutler, SD, Sinclair, K, Abou El Hassan, M, Greer, W, Goudie, M, Wagner, J, White, D , Couban, S, Forward, N, Gaston, D & Campbell, CJV 2019, 'Low-depth sequencing for copy number abnormalities in multiple myeloma supersedes fluorescent in situ hybridization in scope and resolution', Clinical Genetics, 卷 96, 号码 2, 页码 163-168. https://doi.org/10.1111/cge.13561

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author = "Elnenaei, {Manal O.} and Philipp Knopf and Cutler, {Samuel D.} and Keaton Sinclair and {Abou El Hassan}, Mohamed and Wenda Greer and Marissa Goudie and Julie Wagner and Darrell White and Stephen Couban and Nicholas Forward and Daniel Gaston and Campbell, {Clinton J.V.}",

note = "Funding Information: We thank Makoto Matsuoka, Judy Park and Kendra MacDonald for excellent technical assistance and the Molecular Diagnostics Laboratory at the IWK Hospital for their valuable assistance. This study was supported by a Nova Scotia Health Authority Research grant (#1021270). Illumina provided the reagents for library preparation and flow cell for sequencing. Publisher Copyright: {\textcopyright} 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd",

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doi = "10.1111/cge.13561",

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AU - Elnenaei, Manal O.

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AU - Cutler, Samuel D.

AU - Sinclair, Keaton

AU - Abou El Hassan, Mohamed

AU - Greer, Wenda

AU - Goudie, Marissa

AU - Wagner, Julie

AU - White, Darrell

AU - Couban, Stephen

AU - Forward, Nicholas

AU - Gaston, Daniel

AU - Campbell, Clinton J.V.

N1 - Funding Information: We thank Makoto Matsuoka, Judy Park and Kendra MacDonald for excellent technical assistance and the Molecular Diagnostics Laboratory at the IWK Hospital for their valuable assistance. This study was supported by a Nova Scotia Health Authority Research grant (#1021270). Illumina provided the reagents for library preparation and flow cell for sequencing. Publisher Copyright: © 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd

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Low-depth sequencing for copy number abnormalities in multiple myeloma supersedes fluorescent in situ hybridization in scope and resolution

!!!ASJC Scopus Subject Areas

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