Systematic analysis of genetic alterations in tumors using Cancer Genome WorkBench (CGWB). (Q35854835)

10 August 2017

Systematic analysis of genetic alterations in tumors using Cancer Genome WorkBench (CGWB). (English)

1 reference

10 August 2017

Jeffery P Struewing

8

0 references

Kenneth H. Buetow

9

object named as

Kenneth H Buetow

1 reference

10 August 2017

Jinghui Zhang

1

1 reference

10 August 2017

Richard P Finney

2

1 reference

10 August 2017

William Rowe

3

1 reference

10 August 2017

Michael Edmonson

4

1 reference

10 August 2017

Sei Hoon Yang

5

1 reference

10 August 2017

Tatiana Dracheva

6

1 reference

10 August 2017

Jin Jen

7

1 reference

10 August 2017

24 May 2007

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10 August 2017

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10 August 2017

17

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10 August 2017

7

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10 August 2017

1111-1117

1 reference

Automating resequencing-based detection of insertion-deletion polymorphisms

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

Commonly studied single-nucleotide polymorphisms and breast cancer: results from the Breast Cancer Association Consortium

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

The consensus coding sequences of human breast and colorectal cancers

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

Database resources of the National Center for Biotechnology Information

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

SNPdetector: a software tool for sensitive and accurate SNP detection

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

Mutations in the tyrosine kinase domain of the epidermal growth factor receptor in non-small cell lung cancer

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

Comprehensive identification and characterization of diallelic insertion-deletion polymorphisms in 330 human candidate genes

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

Cancer genes and the pathways they control

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to gefitinib

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

HapScope: a software system for automated and visual analysis of functionally annotated haplotypes

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

Inactivation of LKB1/STK11 is a common event in adenocarcinomas of the lung

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

The human genome browser at UCSC

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

Consed: a graphical tool for sequence finishing

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

Base-calling of automated sequencer traces using phred. I. Accuracy assessment

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

Cn3D: a new generation of three-dimensional molecular structure viewer

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

Transforming genes of carcinomas and neuroblastomas introduced into mouse fibroblasts

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

Mutation and cancer: statistical study of retinoblastoma

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

A space-efficient algorithm for local similarities.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

InSNP: a tool for automated detection and visualization of SNPs and InDels

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

An exhaustive DNA micro-satellite map of the human genome using high performance computing.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1899122

Mutations and polymorphisms in the familial early-onset breast cancer (BRCA1) gene. Breast Cancer Information Core

24 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17525135

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Sensitive mutation detection in heterogeneous cancer specimens by massively parallel picoliter reactor sequencing

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17525135

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1101/GR.5963407

1 reference

10 August 2017

1 reference

10 August 2017

PubMed publication ID

17525135

1 reference