Shimmer: detection of genetic alterations in tumors using next-generation sequence data (Q34688498)

3 August 2017

title

Shimmer: detection of genetic alterations in tumors using next-generation sequence data (English)

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3 August 2017

Yardena Samuels

4

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James C Mullikin

series ordinal

5

object named as

James C Mullikin

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3 August 2017

Nancy F Hansen

1

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3 August 2017

Jared J Gartner

series ordinal

2

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3 August 2017

Lan Mei

series ordinal

3

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3 August 2017

language of work or name

English

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publication date

24 April 2013

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3 August 2017

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3 August 2017

volume

29

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3 August 2017

issue

12

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3 August 2017

page(s)

1498-1503

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Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples

3 August 2017

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1 reference

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7 July 2018

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Absolute quantification of somatic DNA alterations in human cancer

7 July 2018

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7 July 2018

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7 July 2018

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Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing

7 July 2018

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VarSifter: visualizing and analyzing exome-scale sequence variation data on a desktop computer

7 July 2018

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Frequent somatic mutations in MAP3K5 and MAP3K9 in metastatic melanoma identified by exome sequencing

7 July 2018

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Antitumor activity of BRAF inhibitor vemurafenib in preclinical models of BRAF-mutant colorectal cancer

7 July 2018

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SomaticSniper: identification of somatic point mutations in whole genome sequencing data

7 July 2018

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Feature-based classifiers for somatic mutation detection in tumour-normal paired sequencing data

7 July 2018

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A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data

7 July 2018

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Frequent mutations of chromatin remodeling genes in transitional cell carcinoma of the bladder

7 July 2018

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7 July 2018

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Exome sequencing identifies GRIN2A as frequently mutated in melanoma

7 July 2018

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The genomic complexity of primary human prostate cancer

7 July 2018

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Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing

7 July 2018

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ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

7 July 2018

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The mutation spectrum revealed by paired genome sequences from a lung cancer patient

7 July 2018

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International network of cancer genome projects

7 July 2018

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A comprehensive catalogue of somatic mutations from a human cancer genome

7 July 2018

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How does multiple testing correction work?

7 July 2018

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7 July 2018

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Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution

7 July 2018

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The Sequence Alignment/Map format and SAMtools

7 July 2018

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ErbB receptors: from oncogenes to targeted cancer therapies

7 July 2018

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The International HapMap Project

7 July 2018

1 reference

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Reliable detection of subclonal single-nucleotide variants in tumour cell populations.

7 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTT183

10.1093/BIOINFORMATICS/BTT183

21 January 2018

Identifiers

DOI

1 reference

journals/bioinformatics/HansenGMSM13

3 August 2017

DBLP publication ID

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

3 August 2017

1 reference