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Molecular etiology of an indolent lymphoproliferative disorder determined by whole-genome sequencing
In an attempt to assess potential treatment options, whole-genome and transcriptome sequencing were performed on a patient with an unclassifiable small lymphoproliferative disorder. Variants from genome sequencing were prioritized using a combination of comparative variant distributions in a spectru...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4849852/ https://www.ncbi.nlm.nih.gov/pubmed/27148583 http://dx.doi.org/10.1101/mcs.a000679 |
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author | Parker, Jeremy D.K. Shen, Yaoqing Pleasance, Erin Li, Yvonne Schein, Jacqueline E. Zhao, Yongjun Moore, Richard Wegrzyn-Woltosz, Joanna Savage, Kerry J. Weng, Andrew P. Gascoyne, Randy D. Jones, Steven Marra, Marco Laskin, Janessa Karsan, Aly |
author_facet | Parker, Jeremy D.K. Shen, Yaoqing Pleasance, Erin Li, Yvonne Schein, Jacqueline E. Zhao, Yongjun Moore, Richard Wegrzyn-Woltosz, Joanna Savage, Kerry J. Weng, Andrew P. Gascoyne, Randy D. Jones, Steven Marra, Marco Laskin, Janessa Karsan, Aly |
author_sort | Parker, Jeremy D.K. |
collection | PubMed |
description | In an attempt to assess potential treatment options, whole-genome and transcriptome sequencing were performed on a patient with an unclassifiable small lymphoproliferative disorder. Variants from genome sequencing were prioritized using a combination of comparative variant distributions in a spectrum of lymphomas, and meta-analyses of gene expression profiling. In this patient, the molecular variants that we believe to be most relevant to the disease presentation most strongly resemble a diffuse large B-cell lymphoma (DLBCL), whereas the gene expression data are most consistent with a low-grade chronic lymphocytic leukemia (CLL). The variant of greatest interest was a predicted NOTCH2-truncating mutation, which has been recently reported in various lymphomas. |
format | Online Article Text |
id | pubmed-4849852 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-48498522016-05-04 Molecular etiology of an indolent lymphoproliferative disorder determined by whole-genome sequencing Parker, Jeremy D.K. Shen, Yaoqing Pleasance, Erin Li, Yvonne Schein, Jacqueline E. Zhao, Yongjun Moore, Richard Wegrzyn-Woltosz, Joanna Savage, Kerry J. Weng, Andrew P. Gascoyne, Randy D. Jones, Steven Marra, Marco Laskin, Janessa Karsan, Aly Cold Spring Harb Mol Case Stud Research Report In an attempt to assess potential treatment options, whole-genome and transcriptome sequencing were performed on a patient with an unclassifiable small lymphoproliferative disorder. Variants from genome sequencing were prioritized using a combination of comparative variant distributions in a spectrum of lymphomas, and meta-analyses of gene expression profiling. In this patient, the molecular variants that we believe to be most relevant to the disease presentation most strongly resemble a diffuse large B-cell lymphoma (DLBCL), whereas the gene expression data are most consistent with a low-grade chronic lymphocytic leukemia (CLL). The variant of greatest interest was a predicted NOTCH2-truncating mutation, which has been recently reported in various lymphomas. Cold Spring Harbor Laboratory Press 2016-03 /pmc/articles/PMC4849852/ /pubmed/27148583 http://dx.doi.org/10.1101/mcs.a000679 Text en © 2016 Parker et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/) , which permits reuse and redistribution, except for commercial purposes, provided that the original author and source are credited. |
spellingShingle | Research Report Parker, Jeremy D.K. Shen, Yaoqing Pleasance, Erin Li, Yvonne Schein, Jacqueline E. Zhao, Yongjun Moore, Richard Wegrzyn-Woltosz, Joanna Savage, Kerry J. Weng, Andrew P. Gascoyne, Randy D. Jones, Steven Marra, Marco Laskin, Janessa Karsan, Aly Molecular etiology of an indolent lymphoproliferative disorder determined by whole-genome sequencing |
title | Molecular etiology of an indolent lymphoproliferative disorder determined by whole-genome sequencing |
title_full | Molecular etiology of an indolent lymphoproliferative disorder determined by whole-genome sequencing |
title_fullStr | Molecular etiology of an indolent lymphoproliferative disorder determined by whole-genome sequencing |
title_full_unstemmed | Molecular etiology of an indolent lymphoproliferative disorder determined by whole-genome sequencing |
title_short | Molecular etiology of an indolent lymphoproliferative disorder determined by whole-genome sequencing |
title_sort | molecular etiology of an indolent lymphoproliferative disorder determined by whole-genome sequencing |
topic | Research Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4849852/ https://www.ncbi.nlm.nih.gov/pubmed/27148583 http://dx.doi.org/10.1101/mcs.a000679 |
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