(Q34720177)

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Comprehensive analysis of loss of heterozygosity events in glioblastoma using the 100K SNP mapping arrays and comparison with copy number abnormalities defined by BAC array comparative genomic hybridization.

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28 December 2019

Comprehensive analysis of loss of heterozygosity events in glioblastoma using the 100K SNP mapping arrays and comparison with copy number abnormalities defined by BAC array comparative genomic hybridization (English)

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28 December 2019

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28 December 2019

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Yaron Turpaz

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28 December 2019

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Ken C Lo

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28 December 2019

Dione Bailey

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28 December 2019

Tania Burkhardt

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28 December 2019

Paul Gardina

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28 December 2019

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1 March 2008

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28 December 2019

Genes, Chromosomes and Cancer

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28 December 2019

47

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28 December 2019

3

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28 December 2019

221-237

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28 December 2019

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

1 reference

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Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.

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High-resolution global genomic survey of 178 gliomas reveals novel regions of copy number alteration and allelic imbalances

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Overlay analysis of the oligonucleotide array gene expression profiles and copy number abnormalities as determined by array comparative genomic hybridization in medulloblastomas

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Candidate glioblastoma development gene identification using concordance between copy number abnormalities and gene expression level changes.

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Genome wide copy number abnormalities in pediatric medulloblastomas as assessed by array comparative genome hybridization

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Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays.

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

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Association of p53 genetic polymorphism (Arg72Pro) with estrogen receptor positive breast cancer risk in Japanese women

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

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p53 codon 72 polymorphism in vulval cancer and vulval intraepithelial neoplasia

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Novel amplicons on the short arm of chromosome 7 identified using high resolution array CGH contain over expressed genes in addition to EGFR in glioblastoma multiforme.

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Identification of consistent novel submegabase deletions in low-grade oligodendrogliomas using array-based comparative genomic hybridization

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A new look towards BAC-based array CGH through a comprehensive comparison with oligo-based array CGH.

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

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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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A p53 polymorphism modifies the risk of hepatocellular carcinoma among non-carriers but not carriers of chronic hepatitis B virus infection

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10.1002/GCC.20524

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18050302%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18050302%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

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