Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization. (Q36465662)

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9 January 2020

title

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

1 reference

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9 January 2020

5

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9 January 2020

Barbara E. Stranger

8

1 reference

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9 January 2020

John Marioni

1

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9 January 2020

Armand Valsesia

3

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9 January 2020

Tomas Fitzgerald

4

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9 January 2020

Dan Andrews

7

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9 January 2020

Andy G. Lynch

9

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author name string

Natalie P Thorne

2

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9 January 2020

Heike Fiegler

6

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9 January 2020

Emmanouil T Dermitzakis

10

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9 January 2020

Nigel P Carter

11

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9 January 2020

Simon Tavaré

12

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9 January 2020

Matthew E Hurles

13

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publication date

1 January 2007

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9 January 2020

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volume

8

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issue

10

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9 January 2020

page(s)

R228

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describes a project that uses

9 January 2020

limma

object named as

limma

2 references

22 June 2022

https://europepmc.org/article/PMC/2246302

based on heuristic

inferred from PubMed Central ID database lookup

CZ Software Mentions: A large dataset of software mentions in the biomedical literature

cites work

A comprehensive analysis of common copy-number variations in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2246302

Global variation in copy number in the human genome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2246302

Accurate and reliable high-throughput detection of copy number variation in the human genome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2246302

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2246302

Mapping tumor-suppressor genes with multipoint statistics from copy-number-variation data

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2246302

A haplotype map of the human genome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2246302

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2246302

High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridization

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2246302

CGHcall: calling aberrations for array CGH tumor profiles.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2246302

Detection of gene copy number changes in CGH microarrays using a spatially correlated mixture model.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2246302

A pseudolikelihood approach for simultaneous analysis of array comparative genomic hybridizations

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2246302

A high-resolution survey of deletion polymorphism in the human genome

21 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17961237

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/GB-2007-8-10-R228

1 reference

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Dimensions Publication ID

9 January 2020

0 references

1 reference

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9 January 2020

PubMed publication ID

17961237

1 reference