(Q44054130)

29 November 2017

title

A Bayesian segmentation approach to ascertain copy number variations at the population level (English)

1 reference

29 November 2017

Long Yang Wu

1

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29 November 2017

Hugh A Chipman

2

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29 November 2017

Shelley B Bull

3

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29 November 2017

Laurent Briollais

4

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29 November 2017

Kesheng Wang

5

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29 November 2017

language of work or name

English

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publication date

23 April 2009

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29 November 2017

number of pages

11

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based on heuristic

inferred from page(s)

published in

Bioinformatics

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29 November 2017

volume

25

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29 November 2017

issue

13

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29 November 2017

page(s)

1669-1679

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

29 November 2017

cites work

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21 January 2018

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Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies

21 January 2018

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Structural variation in the human genome

21 January 2018

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

21 January 2018

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

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CD38 is critical for social behaviour by regulating oxytocin secretion

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21 January 2018

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Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome

21 January 2018

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Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

21 January 2018

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Accounting for haplotype uncertainty in matched association studies: a comparison of simple and flexible techniques.

21 January 2018

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Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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10.1093/BIOINFORMATICS/BTP270

21 January 2018

Identifiers

DOI

1 reference

journals/bioinformatics/WuCBBW09

29 November 2017

DBLP publication ID

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference