(Q33903385)

29 July 2017

title

A fast and accurate method to detect allelic genomic imbalances underlying mosaic rearrangements using SNP array data (English)

1 reference

Benjamín Rodríguez-Santiago

29 July 2017

4

Roger Pique-Regi

0 references

object named as

Benjamín Rodríguez-Santiago

2

0 references

Juan R. González

object named as

Juan R González

1

0 references

Stephen Chanock

6

object named as

Stephen J Chanock

1 reference

29 July 2017

5

Nathaniel Rothman

1 reference

29 July 2017

Alejandro Cáceres

3

1 reference

29 July 2017

Lluís Armengol

7

1 reference

29 July 2017

Luis A Pérez-Jurado

8

1 reference

29 July 2017

language of work or name

1 reference

17 May 2011

1 reference

29 July 2017

1 reference

29 July 2017

volume

12

1 reference

29 July 2017

page(s)

166

1 reference

Creative Commons Attribution 2.0 Generic

29 July 2017

copyright license

start time

17 May 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

exact match

https://scigraph.springernature.com/pub.10.1186/1471-2105-12-166

0 references

cites work

R-Gada: a fast and flexible pipeline for copy number analysis in association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118168

Mosaic uniparental disomies and aneuploidies as large structural variants of the human genome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118168

Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118168

Comparing CNV detection methods for SNP arrays

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118168

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118168

Genomic imbalances in neonates with birth defects: high detection rates by using chromosomal microarray analysis.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118168

Segmentation-based detection of allelic imbalance and loss-of-heterozygosity in cancer cells using whole genome SNP arrays

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118168

Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118168

Sparse representation and Bayesian detection of genome copy number alterations from microarray data

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118168

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118168

Spatial smoothing and hot spot detection for CGH data using the fused lasso

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118168

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118168

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118168

Global variation in copy number in the human genome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118168

Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118168

NAT2 slow acetylation, GSTM1 null genotype, and risk of bladder cancer: results from the Spanish Bladder Cancer Study and meta-analyses

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118168

Detection of large-scale variation in the human genome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118168

Large-scale copy number polymorphism in the human genome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118168

Mechanisms and consequences of somatic mosaicism in humans

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118168

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118168

Fine-scale structural variation of the human genome

28 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2105-12-166

Origins and functional impact of copy number variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2105-12-166

Detection of low-level mosaicism and placental mosaicism by oligonucleotide array comparative genomic hybridization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2105-12-166

Association of common copy number variants at the glutathione S-transferase genes and rare novel genomic changes with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2105-12-166

Rapid, high throughput prenatal detection of aneuploidy using a novel quantitative method (MLPA).

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2105-12-166

Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118168

Somatic mosaicism for copy number variation in differentiated human tissues

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21586113

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Detection of low-level mosaicism by array CGH in routine diagnostic specimens

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21586113

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2105-12-166

1 reference

journals/bmcbi/GonzalezRCPRCAP11

29 July 2017

DBLP publication ID

1 reference

DBLP Dataset 2021-01-02

Dimensions Publication ID

28 January 2021

0 references

1 reference

29 July 2017

1 reference