Literature DB >> 22160009

Genomics of AML: clinical applications of next-generation sequencing.

John S Welch1, Daniel C Link.   

Abstract

In the past decade, a series of technological advances have revolutionized our ability to interrogate cancer genomes, culminating in whole-genome sequencing, which provides genome-wide coverage at a single base-pair resolution. As sequencing technologies improve and costs decrease, it is likely that whole-genome sequencing of cancer cells will become commonplace in the diagnostic workup of patients with acute myelogenous leukemia (AML) and other cancers. The unprecedented molecular characterization provided by whole-genome sequencing offers the potential for an individualized approach to treatment in AML, bringing us one step closer to personalized medicine. In this chapter, we discuss how next-generation sequencing is being used to study cancer genomes. Recent publications of whole-genome sequencing in AML are reviewed and current limitations of whole-genome sequencing are examined, as well as current and potential future clinical applications of whole-genome sequencing.

Entities:  

Mesh:

Year:  2011        PMID: 22160009     DOI: 10.1182/asheducation-2011.1.30

Source DB:  PubMed          Journal:  Hematology Am Soc Hematol Educ Program        ISSN: 1520-4383


  20 in total

1.  Analysis of hepatitis C virus intrahost diversity across the coding region by ultradeep pyrosequencing.

Authors:  Michael Lauck; Mónica V Alvarado-Mora; Ericka A Becker; Dipankar Bhattacharya; Rob Striker; Austin L Hughes; Flair J Carrilho; David H O'Connor; João R Rebello Pinho
Journal:  J Virol       Date:  2012-01-25       Impact factor: 5.103

Review 2.  Genomic tools in acute myeloid leukemia: From the bench to the bedside.

Authors:  Brian S White; John F DiPersio
Journal:  Cancer       Date:  2014-01-28       Impact factor: 6.860

3.  Should clinical hematologists put their microscopes on eBay?

Authors:  Mars van't Veer; Torsten Haferlach
Journal:  Haematologica       Date:  2014-10       Impact factor: 9.941

4.  Aberrant RNA splicing and mutations in spliceosome complex in acute myeloid leukemia.

Authors:  Jianbiao Zhou; Wee-Joo Chng
Journal:  Stem Cell Investig       Date:  2017-02-09

5.  FLT3-ITD-associated gene-expression signatures in NPM1-mutated cytogenetically normal acute myeloid leukemia.

Authors:  Liang Huang; Kuangguo Zhou; Yunfan Yang; Zhen Shang; Jue Wang; Di Wang; Na Wang; Danmei Xu; Jianfeng Zhou
Journal:  Int J Hematol       Date:  2012-06-12       Impact factor: 2.490

6.  PAX5 alteration-associated gene-expression signatures in B-cell acute lymphoblastic leukemia.

Authors:  Zhen Shang; Yuechao Zhao; Kuangguo Zhou; Yanling Xu; Wei Huang
Journal:  Int J Hematol       Date:  2013-03-26       Impact factor: 2.490

Review 7.  Are results of targeted gene sequencing ready to be used for clinical decision making for patients with acute myelogenous leukemia?

Authors:  Arati V Rao; B Douglas Smith
Journal:  Curr Hematol Malig Rep       Date:  2013-06       Impact factor: 3.952

8.  Heterogeneity of clonal expansion and maturation-linked mutation acquisition in hematopoietic progenitors in human acute myeloid leukemia.

Authors:  R B Walter; G S Laszlo; J M Lionberger; J A Pollard; K H Harrington; C J Gudgeon; M Othus; S Rafii; S Meshinchi; F R Appelbaum; I D Bernstein
Journal:  Leukemia       Date:  2014-03-18       Impact factor: 11.528

Review 9.  Solving the molecular diagnostic testing conundrum for Mendelian disorders in the era of next-generation sequencing: single-gene, gene panel, or exome/genome sequencing.

Authors:  Yuan Xue; Arunkanth Ankala; William R Wilcox; Madhuri R Hegde
Journal:  Genet Med       Date:  2014-09-18       Impact factor: 8.822

10.  Next-generation sequencing: application in liver cancer-past, present and future?

Authors:  Jens U Marquardt; Jesper B Andersen
Journal:  Biology (Basel)       Date:  2012-08-31
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