Detection of mutations in myeloid malignancies through paired-sample analysis of microdroplet-PCR deep sequencing data. (Q30836256)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25017477%20AND%20SRC:MED&resulttype=core&format=json

9 March 2020

title

Detection of mutations in myeloid malignancies through paired-sample analysis of microdroplet-PCR deep sequencing data (English)

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9 March 2020

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12

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9 March 2020

author name string

Donavan T Cheng

1

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9 March 2020

Janice Cheng

2

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9 March 2020

Talia N Mitchell

3

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9 March 2020

Aijazuddin Syed

4

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9 March 2020

Ahmet Zehir

5

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9 March 2020

Nana Yaa T Mensah

6

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9 March 2020

Alifya Oultache

7

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9 March 2020

Khedoudja Nafa

8

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9 March 2020

Ross L Levine

9

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9 March 2020

Maria E Arcila

10

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9 March 2020

Michael F Berger

11

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9 March 2020

publication date

10 July 2014

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The Journal of Molecular Diagnostics

9 March 2020

published in

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volume

16

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9 March 2020

page(s)

504-518

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9 March 2020

issue

5

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Clinical validation of a next-generation sequencing screen for mutational hotspots in 46 cancer-related genes.

9 March 2020

cites work

1 reference

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14 July 2018

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14 July 2018

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14 July 2018

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14 July 2018

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14 July 2018

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Prevalence and prognostic implications of WT1 mutations in pediatric acute myeloid leukemia (AML): a report from the Children's Oncology Group.

14 July 2018

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DNA methylation signatures identify biologically distinct subtypes in acute myeloid leukemia.

14 July 2018

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Microdroplet-based PCR enrichment for large-scale targeted sequencing

14 July 2018

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Recurring mutations found by sequencing an acute myeloid leukemia genome

14 July 2018

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Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads

14 July 2018

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VarScan: variant detection in massively parallel sequencing of individual and pooled samples

14 July 2018

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Fast and accurate short read alignment with Burrows-Wheeler transform

14 July 2018

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Keeping up with the next generation: massively parallel sequencing in clinical diagnostics

14 July 2018

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A decade of genome-wide gene expression profiling in acute myeloid leukemia: flashback and prospects

14 July 2018

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Mutations and treatment outcome in cytogenetically normal acute myeloid leukemia

14 July 2018

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14 July 2018

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Role of JAK2 in the pathogenesis and therapy of myeloproliferative disorders

14 July 2018

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Acute myeloid leukemia carrying cytoplasmic/mutated nucleophosmin (NPMc+ AML): biologic and clinical features

14 July 2018

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MPLW515L is a novel somatic activating mutation in myelofibrosis with myeloid metaplasia

14 July 2018

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Activating mutation of D835 within the activation loop of FLT3 in human hematologic malignancies

14 July 2018

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Dominant-negative mutations of CEBPA, encoding CCAAT/enhancer binding protein-alpha (C/EBPalpha), in acute myeloid leukemia

14 July 2018

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Internal tandem duplication of the FLT3 gene is preferentially seen in acute myeloid leukemia and myelodysplastic syndrome among various hematological malignancies. A study on a large series of patients and cell lines

14 July 2018

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14 July 2018

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25 November 2018

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WT1 mutation in 470 adult patients with acute myeloid leukemia: stability during disease evolution and implication of its incorporation into a survival scoring system.

25 November 2018

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25 November 2018

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Mutations in the gene encoding the transcription factor CCAAT/enhancer binding protein alpha in myelodysplastic syndromes and acute myeloid leukemias

25 November 2018

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25 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25017477

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Next-generation sequencing applied to molecular diagnostics

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25017477

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.JMOLDX.2014.05.006

1 reference

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9 March 2020

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9 March 2020

1 reference

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