DiNAMIC: a method to identify recurrent DNA copy number aberrations in tumors (Q30498218)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21183584%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

title

DiNAMIC: a method to identify recurrent DNA copy number aberrations in tumors (English)

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18 January 2020

1

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18 January 2020

author name string

Andrew B Nobel

series ordinal

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21183584%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

Fred A Wright

series ordinal

3

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18 January 2020

language of work or name

English

0 references

publication date

23 December 2010

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21183584%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

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18 January 2020

volume

27

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18 January 2020

issue

5

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18 January 2020

page(s)

678-685

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LocusZoom: regional visualization of genome-wide association scan results

18 January 2020

cites work

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Integrated study of copy number states and genotype calls using high-density SNP arrays

28 July 2018

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28 July 2018

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Computational methods for identification of recurrent copy number alteration patterns by array CGH.

28 July 2018

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Population analysis of large copy number variants and hotspots of human genetic disease

28 July 2018

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Identification of cancer genes using a statistical framework for multiexperiment analysis of nondiscretized array CGH data

28 July 2018

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Assessing the significance of chromosomal aberrations in cancer: methodology and application to glioma

28 July 2018

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Genome-wide DNA copy number analysis in pancreatic cancer using high-density single nucleotide polymorphism arrays

28 July 2018

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Assessment of algorithms for high throughput detection of genomic copy number variation in oligonucleotide microarray data

28 July 2018

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Assessing the significance of conserved genomic aberrations using high resolution genomic microarrays

28 July 2018

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A faster circular binary segmentation algorithm for the analysis of array CGH data

28 July 2018

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Global variation in copy number in the human genome

28 July 2018

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Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays

28 July 2018

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High-resolution global genomic survey of 178 gliomas reveals novel regions of copy number alteration and allelic imbalances

28 July 2018

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STAC: A method for testing the significance of DNA copy number aberrations across multiple array-CGH experiments

28 July 2018

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Manifestation, mechanisms and mysteries of gene amplifications

28 July 2018

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The natural history of EGFR and EGFRvIII in glioblastoma patients

28 July 2018

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Array CGH technologies and their applications to cancer genomes

28 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042182

Circular binary segmentation for the analysis of array-based DNA copy number data

28 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042182

An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays

28 July 2018

1 reference

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Pooled analysis of loss of heterozygosity in breast cancer: a genome scan provides comparative evidence for multiple tumor suppressors and identifies novel candidate regions

28 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042182

Chromosome aberrations in solid tumors

28 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042182

The human genome browser at UCSC

28 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042182

Expression of SET, an inhibitor of protein phosphatase 2A, in renal development and Wilms' tumor

28 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042182

On the statistical analysis of allelic-loss data

28 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042182

Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12–q21

28 July 2018

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Smoothing waves in array CGH tumor profiles

28 July 2018

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Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization.

26 November 2018

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Resolving the resolution of array CGH.

26 November 2018

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Genetic alterations in cancer knowledge system: analysis of gene mutations in mouse and human liver and lung tumors

26 November 2018

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Analysis of array CGH data: from signal ratio to gain and loss of DNA regions

26 November 2018

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Inferring the location of tumor suppressor genes by modeling frequency of allelic loss

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21183584

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Array CGH profiling of favourable histology Wilms tumours reveals novel gains and losses associated with relapse

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21183584

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

An improved Bonferroni procedure for multiple tests of significance

1 reference

19 June 2022

https://opencitations.net/index/coci/api/v1/citations/10.1093/BIOMET/73.3.751

Identifiers

DOI

10.1093/BIOINFORMATICS/BTQ717

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21183584%20AND%20SRC:MED&resulttype=core&format=json

journals/bioinformatics/WalterNW11

18 January 2020

DBLP publication ID

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21183584%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

PubMed publication ID

21183584

1 reference