(Q34772601)

English

Accurately identifying low-allelic fraction variants in single samples with next-generation sequencing: applications in tumor subclone resolution

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

Accurately identifying low-allelic fraction variants in single samples with next-generation sequencing: applications in tumor subclone resolution (English)

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

object named as

Lucy F Stead

1

0 references

object named as

Philip Quirke

4

0 references

author name string

Kate M Sutton

2

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

Graham R Taylor

3

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

Pamela Rabbitts

5

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

publication date

11 July 2013

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

34

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

10

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

1432-1438

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

describes a project that uses

massive parallel sequencing

1 reference

based on heuristic

inferred from title

Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

An integrative variant analysis suite for whole exome next-generation sequencing data

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

Mutation detection by clonal sequencing of PCR amplicons and grouped read typing is applicable to clinical diagnostics

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

A framework for variation discovery and genotyping using next-generation DNA sequencing data

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

GENCODE: the reference human genome annotation for The ENCODE Project

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

BayesCall: A model-based base-calling algorithm for high-throughput short-read sequencing

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

High-throughput DNA sequencing--concepts and limitations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

The UCSC genome browser database: update 2007.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

Fast and accurate short read alignment with Burrows-Wheeler transform

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

Sequence-specific error profile of Illumina sequencers

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

The life history of 21 breast cancers

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

JointSNVMix: a probabilistic model for accurate detection of somatic mutations in normal/tumour paired next-generation sequencing data

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

Strelka: accurate somatic small-variant calling from sequenced tumor-normal sample pairs

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

Next-generation DNA sequencing

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

dbSNP: the NCBI database of genetic variation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

Clonal architecture of secondary acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

SNVer: a statistical tool for variant calling in analysis of pooled or individual next-generation sequencing data

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

LoFreq: a sequence-quality aware, ultra-sensitive variant caller for uncovering cell-population heterogeneity from high-throughput sequencing datasets

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22365

21 January 2018

Identifiers

10.1002/HUMU.22365

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q34772601&oldid=1878884547"