(Q25257143)

6 July 2017

CARAT: a novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays (English)

1 reference

6 July 2017

9

Hiroyuki Aburatani

1 reference

6 July 2017

Jing Huang

1

1 reference

6 July 2017

Wen Wei

2

1 reference

6 July 2017

Joyce Chen

3

1 reference

6 July 2017

Jane Zhang

4

1 reference

6 July 2017

Guoying Liu

5

1 reference

6 July 2017

Xiaojun Di

6

1 reference

6 July 2017

Rui Mei

7

1 reference

6 July 2017

Shumpei Ishikawa

8

1 reference

6 July 2017

Keith W Jones

10

1 reference

6 July 2017

Michael H Shapero

11

1 reference

6 July 2017

language of work or name

English

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publication date

21 February 2006

1 reference

6 July 2017

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6 July 2017

7

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6 July 2017

1

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page(s)

83

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2105-7-83

6 July 2017

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7 April 2017

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7 April 2017

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7 April 2017

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7 April 2017

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Light-generated oligonucleotide arrays for rapid DNA sequence analysis

7 April 2017

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Detection and mapping of amplified DNA sequences in breast cancer by comparative genomic hybridization

7 April 2017

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Structural variation in the human genome

7 April 2017

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Fine-scale structural variation of the human genome

7 April 2017

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Detection of large-scale variation in the human genome

7 April 2017

1 reference

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Segmental duplications and copy-number variation in the human genome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Large-scale copy number polymorphism in the human genome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation

7 April 2017

1 reference

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Genome-wide detection of allelic imbalance using human SNPs and high-density DNA arrays

7 April 2017

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A DNA polymorphism discovery resource for research on human genetic variation

7 April 2017

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Restriction landmark genomic scanning method and its various applications

7 April 2017

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Studies of the HER-2/neu proto-oncogene in human breast and ovarian cancer

7 April 2017

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Genome-wide analysis of DNA copy-number changes using cDNA microarrays

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

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

7 April 2017

1 reference

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Genome-wide copy number analysis on GeneChip platform using copy number analyzer for affymetrix GeneChip 2.0 software

7 April 2017

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

28 September 2017

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The new cytogenetics: blurring the boundaries with molecular biology

28 September 2017

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

28 September 2017

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Homozygous deletions and chromosome amplifications in human lung carcinomas revealed by single nucleotide polymorphism array analysis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Allelic dosage analysis with genotyping microarrays.

28 September 2017

1 reference

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A method for calling gains and losses in array CGH data

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Comparative genomic hybridization using oligonucleotide microarrays and total genomic DNA.

28 September 2017

1 reference

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Molecular karyotyping using an SNP array for genomewide genotyping.

28 September 2017

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

A versatile statistical analysis algorithm to detect genome copy number variation

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Concurrent analysis of loss of heterozygosity (LOH) and copy number abnormality (CNA) for oral premalignancy progression using the Affymetrix 10K SNP mapping array

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

High-resolution global profiling of genomic alterations with long oligonucleotide microarray

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Allelic imbalance analysis by high-density single-nucleotide polymorphic allele (SNP) array with whole genome amplified DNA.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

High-resolution single-nucleotide polymorphism array and clustering analysis of loss of heterozygosity in human lung cancer cell lines

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

dChipSNP: significance curve and clustering of SNP-array-based loss-of-heterozygosity data

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

High-resolution analysis of DNA copy number using oligonucleotide microarrays

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Microarray analysis reveals a major direct role of DNA copy number alteration in the transcriptional program of human breast tumors

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Assembly of microarrays for genome-wide measurement of DNA copy number

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Multicolor Spectral Karyotyping of Human Chromosomes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Cloning the differences between two complex genomes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Multiplexed biochemical assays with biological chips

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Light-directed, spatially addressable parallel chemical synthesis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

ERBB2 amplification in breast cancer analyzed by fluorescence in situ hybridization

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Loss of heterozygosity and its correlation with expression profiles in subclasses of invasive breast cancers

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Common deletion polymorphisms in the human genome.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Common deletions and SNPs are in linkage disequilibrium in the human genome

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Loss of heterozygosity in childhood acute lymphoblastic leukemia detected by genome-wide microarray single nucleotide polymorphism analysis.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

High-resolution analysis of chromosomal imbalances using the Affymetrix 10K SNP genotyping chip.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Dynamic model based algorithms for screening and genotyping over 100 K SNPs on oligonucleotide microarrays.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Large-scale genotyping of complex DNA.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1402331

Genome-wide association study in esophageal cancer using GeneChip mapping 10K array

28 November 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arrays

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2105-7-83

1 reference

journals/bmcbi/HuangWCZLDMIAJS06

6 July 2017

1 reference

DBLP Dataset 2021-01-02

Dimensions Publication ID

28 January 2021

0 references

1 reference

6 July 2017

1 reference