Genome-wide Mapping of Copy Number Variations Using SNP Arrays. - Wikidata - wikimedia - TriplyDB

Genome-wide Mapping of Copy Number Variations Using SNP Arrays.

Genome-wide Mapping of Copy Number Variations Using SNP Arrays.

http://www.wikidata.org/entity/Q34139304

about

Deciphering global signal features of high-throughput array data from cancers.SNP array analysis of acute promyelocytic leukemia may be of prognostic relevance and identifies a potential high risk group with recurrent deletions on chromosomal subband 1q31.3.The 'Whole Genome Age'

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P2860

Genome-wide Mapping of Copy Number Variations Using SNP Arrays.

http://www.wikidata.org/entity/Q34139304

description

2009 nî lūn-bûn

@nan

2009 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年論文

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2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

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2009年论文

@wuu

name

Genome-wide Mapping of Copy Number Variations Using SNP Arrays.

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Genome-wide Mapping of Copy Number Variations Using SNP Arrays.

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Genome-wide Mapping of Copy Number Variations Using SNP Arrays.

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type

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Genome-wide Mapping of Copy Number Variations Using SNP Arrays.

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Genome-wide Mapping of Copy Number Variations Using SNP Arrays.

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Genome-wide Mapping of Copy Number Variations Using SNP Arrays.

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Genome-wide Mapping of Copy Number Variations Using SNP Arrays.

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Genome-wide Mapping of Copy Number Variations Using SNP Arrays.

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Genome-wide Mapping of Copy Number Variations Using SNP Arrays.

@nl

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Transfusion Medicine and Hemotherapy

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Genome-wide Mapping of Copy Number Variations Using SNP Arrays.

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Daniel Nowak

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H Phillip Koeffler

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Wolf-Karsten Hofmann

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P2860

Inferring loss-of-heterozygosity from unpaired tumors using high-density oligonucleotide SNP arrays

Genome-wide detection and characterization of positive selection in human populations

Variations in DNA elucidate molecular networks that cause disease

Shared and distinct genetic variants in type 1 diabetes and celiac disease

Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray

A second generation human haplotype map of over 3.1 million SNPs

Global variation in copy number in the human genome

Genomewide association analysis of coronary artery disease

Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays

A haplotype map of the human genome

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246-251

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scholarly article

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10.1159/000225372

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4

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36

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2009-07-10T00:00:00Z

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47676817

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21049075

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2941829

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