(Q33529487)

27 July 2017

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title

CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics (English)

1 reference

27 July 2017

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Monica D'arcy

5

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Hongbo M. Xie

object named as

Hongbo M Xie

7

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Tamim H Shaikh

9

object named as

Tamim H Shaikh

1 reference

27 July 2017

1

Xiaowu Gai

1 reference

27 July 2017

2

Juan C Perin

1 reference

27 July 2017

8

Eric F Rappaport

1 reference

27 July 2017

Kevin Murphy

3

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27 July 2017

Ryan O'Hara

4

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27 July 2017

Adam Wenocur

6

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27 July 2017

Peter S White

10

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27 July 2017

4 February 2010

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27 July 2017

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27 July 2017

11

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27 July 2017

74

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https://scigraph.springernature.com/pub.10.1186/1471-2105-11-74

27 July 2017

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cites work

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Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

21 June 2018

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Copy number variants, diseases and gene expression

21 June 2018

1 reference

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

21 June 2018

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21 June 2018

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Copy-number variations associated with neuropsychiatric conditions

21 June 2018

1 reference

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PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

21 June 2018

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ACTuDB, a new database for the integrated analysis of array-CGH and clinical data for tumors.

21 June 2018

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Strong association of de novo copy number mutations with autism

21 June 2018

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QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827374

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827374

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

21 June 2018

1 reference

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Global variation in copy number in the human genome

21 June 2018

1 reference

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

21 June 2018

1 reference

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

21 June 2018

1 reference

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High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping

21 June 2018

1 reference

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21 June 2018

1 reference

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Galaxy: a platform for interactive large-scale genome analysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827374

A comparison study: applying segmentation to array CGH data for downstream analyses

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827374

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827374

Segmental duplications and copy-number variation in the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827374

Fine-scale structural variation of the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827374

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827374

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

21 June 2018

1 reference

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Detection of large-scale variation in the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827374

The genetic association database

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827374

Genomic microarrays in human genetic disease and cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827374

The generic genome browser: a building block for a model organism system database

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827374

Common deletion polymorphisms in the human genome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827374

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

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20132550

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2105-11-74

1 reference

journals/bmcbi/GaiPMODWXRSW10

27 July 2017

1 reference

DBLP Dataset 2021-01-02

Dimensions Publication ID

28 January 2021

0 references

1 reference

27 July 2017

1 reference