(Q38072120)

28 August 2017

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title

Next-generation sequencing - feasibility and practicality in haematology (English)

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28 August 2017

4

Torsten Haferlach

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28 August 2017

Alexander Kohlmann

1

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28 August 2017

Vera Grossmann

series ordinal

2

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28 August 2017

Niroshan Nadarajah

series ordinal

3

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28 August 2017

language of work or name

English

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publication date

7 January 2013

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British Journal of Haematology

28 August 2017

published in

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28 August 2017

volume

160

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28 August 2017

issue

6

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28 August 2017

page(s)

736-753

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Direct selection of human genomic loci by microarray hybridization

28 August 2017

cites work

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Initial genome sequencing and analysis of multiple myeloma

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Myelodysplastic syndromes: the complexity of stem-cell diseases

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Statistical Analyses of Next Generation Sequence Data: A Partial Overview

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Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders

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Analysis of the chronic lymphocytic leukemia coding genome: role of NOTCH1 mutational activation

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Field guide to next-generation DNA sequencers

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21 January 2018

Profiles in leukemia.

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21 January 2018

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Whole-exome sequencing identifies somatic mutations of BCOR in acute myeloid leukemia with normal karyotype

21 January 2018

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A novel hierarchical prognostic model of AML solely based on molecular mutations

21 January 2018

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Detection of low prevalence somatic mutations in solid tumors with ultra-deep targeted sequencing

21 January 2018

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TP53 mutations in low-risk myelodysplastic syndromes with del(5q) predict disease progression.

21 January 2018

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Impaired hydroxylation of 5-methylcytosine in myeloid cancers with mutant TET2

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The Interlaboratory RObustness of Next-generation sequencing (IRON) study: a deep sequencing investigation of TET2, CBL and KRAS mutations by an international consortium involving 10 laboratories.

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Somatic STAT3 mutations in large granular lymphocytic leukemia

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DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome

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21 January 2018

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Somatic mutations in the transcriptional corepressor gene BCORL1 in adult acute myelogenous leukemia

21 January 2018

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Performance comparison of benchtop high-throughput sequencing platforms

21 January 2018

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Recurring mutations found by sequencing an acute myeloid leukemia genome

21 January 2018

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SRSF2 mutations in 275 cases with chronic myelomonocytic leukemia (CMML)

21 January 2018

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Sequencing technologies - the next generation

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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BRAF mutations in hairy-cell leukemia

21 January 2018

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21 January 2018

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21 January 2018

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Next generation sequencing for clinical diagnostics-principles and application to targeted resequencing for hypertrophic cardiomyopathy: a paper from the 2009 William Beaumont Hospital Symposium on Molecular Pathology

21 January 2018

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Clonal architecture of secondary acute myeloid leukemia

21 January 2018

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SF3B1 and other novel cancer genes in chronic lymphocytic leukemia

21 January 2018

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The origin and evolution of mutations in acute myeloid leukemia

21 January 2018

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Frequent pathway mutations of splicing machinery in myelodysplasia

21 January 2018

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TP53 mutation and survival in chronic lymphocytic leukemia

21 January 2018

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Analysis of the ABCA4 gene by next-generation sequencing

21 January 2018

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Systematic detection of putative tumor suppressor genes through the combined use of exome and transcriptome sequencing

21 January 2018

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Targeted next-generation sequencing detects point mutations, insertions, deletions and balanced chromosomal rearrangements as well as identifies novel leukemia-specific fusion genes in a single procedure

21 January 2018

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Next-Generation Sequencing Technology Reveals a Characteristic Pattern of Molecular Mutations in 72.8% of Chronic Myelomonocytic Leukemia by Detecting Frequent Alterations in TET2, CBL, RAS, and RUNX1

21 January 2018

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Molecular profiling of chronic myelomonocytic leukemia reveals diverse mutations in >80% of patients with TET2 and EZH2 being of high prognostic relevance

21 January 2018

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21 January 2018

Identifiers

DOI

10.1111/BJH.12194

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28 August 2017

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