High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping (Q35012994)

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Language	Label	Description	Also known as
English	High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

5 August 2017

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

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Europe PubMed Central

PubMed publication ID

5 August 2017

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based on heuristic

inferred from title

whole genome sequencing

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based on heuristic

inferred from title

John W. Belmont

10

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Europe PubMed Central

PubMed publication ID

5 August 2017

9

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Chad A Shaw

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5 August 2017

Frank J Steemers

3

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Frank J Steemers

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5 August 2017

author name string

Daniel A Peiffer

1

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5 August 2017

Jennie M Le

2

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5 August 2017

Weihua Chang

4

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5 August 2017

Tony Jenniges

5

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5 August 2017

Francisco Garcia

6

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5 August 2017

Kirt Haden

7

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5 August 2017

Jiangzhen Li

8

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5 August 2017

Sau Wai Cheung

11

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5 August 2017

Richard M Shen

12

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5 August 2017

David L Barker

13

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5 August 2017

Kevin L Gunderson

14

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5 August 2017

publication date

9 August 2006

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5 August 2017

Genome Research

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5 August 2017

16

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5 August 2017

9

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Europe PubMed Central

PubMed publication ID

5 August 2017

1136-1148

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Europe PubMed Central

PubMed publication ID

5 August 2017

BAC to the future! or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH)

1 reference

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Loss of heterozygosity analyzed by single nucleotide polymorphism array in cancer

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A haplotype map of the human genome

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High-resolution identification of chromosomal abnormalities using oligonucleotide arrays containing 116,204 SNPs

1 reference

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Severe expressive-language delay related to duplication of the Williams-Beuren locus

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Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic event.

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

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Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH.

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A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays

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Global analysis of uniparental disomy using high density genotyping arrays

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Comparative genomic hybridization using oligonucleotide microarrays and total genomic DNA.

1 reference

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Whole genome DNA copy number changes identified by high density oligonucleotide arrays

1 reference

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Cytogenetic characterization of seven human cancer cell lines by combining G- and R-banding, M-FISH, CGH and chromosome- and locus-specific FISH.

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Haploinsufficiency for tumour suppressor genes: when you don't need to go all the way.

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

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High-resolution analysis of DNA copy number using oligonucleotide microarrays

1 reference

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Whole genome amplification of DNA from laser capture-microdissected tissue for high-throughput single nucleotide polymorphism and short tandem repeat genotyping

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Chromosome aberrations in solid tumors

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Genomic microarrays in human genetic disease and cancer

1 reference

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8 July 2018

Digital karyotyping

1 reference

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8 July 2018

Two genetic hits (more or less) to cancer

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Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects

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Laser capture microscopy

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Genome changes and gene expression in human solid tumors

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The Hallmarks of Cancer

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A variant Klinefelter syndrome patient with an XXY/XX/XY karyotype studied by GTG-banding and fluorescence in situ hybridization

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Williams-Beuren syndrome: genes and mechanisms

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High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

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Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances

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Spectral karyotyping, a 24-colour FISH technique for the identification of chromosomal rearrangements

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Loss of heterozygosity or: how I learned to stop worrying and love mitotic recombination

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Multicolour spectral karyotyping of mouse chromosomes

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Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis

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Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndrome

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Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome.

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8 July 2018

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1 reference

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1 reference

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1 reference

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1 reference

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based on heuristic

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Comparison of allelic ratios from paired blood and paraffin-embedded normal tissue for use in a polymerase chain reaction to assess loss of heterozygosity2

1 reference

https://pubmed.ncbi.nlm.nih.gov/16899659

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based on heuristic

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High-density single nucleotide polymorphism array defines novel stage and location-dependent allelic imbalances in human bladder tumors

1 reference

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1 reference

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Rapid detection of loss of heterozygosity of chromosome 17p by polymerase chain reaction-based variable number of tandem repeat analysis and detection of single-strand conformation polymorphism of intragenic p53 polymorphisms

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A tiling resolution DNA microarray with complete coverage of the human genome

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Human breast cancer: frequent p53 allele loss and protein overexpression

1 reference

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12 December 2020

based on heuristic

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Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias

1 reference

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Identifiers

10.1101/GR.5402306

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

ResearchGate publication ID

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