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Single Nucleotide Polymorphism Array

Known as: SNP Genotyping, SNP ARRAY, Genotype Chip 
A genomic microarray-based method able to detect single nucleotide polymorphisms.
National Institutes of Health

Papers overview

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Highly Cited
2014
Highly Cited
2014
High-density single nucleotide polymorphism (SNP) genotyping arrays are a powerful tool for studying genomic patterns of… Expand
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Highly Cited
2010
Highly Cited
2010
Mosaic aneuploidy and uniparental disomy (UPD) arise from mitotic or meiotic events. There are differences between these… Expand
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Highly Cited
2009
Highly Cited
2009
The method for SNP genotyping described in this unit is based on the commercially available Sequenom MassARRAY platform. The… Expand
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Highly Cited
2009
Highly Cited
2009
Background The dissection of complex traits of economic importance to the pig industry requires the availability of a significant… Expand
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Highly Cited
2009
Highly Cited
2009
Myelodysplastic syndromes (MDS) represent a heterogeneous group of neoplastic hematopoietic disorders. Several recurrent… Expand
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Highly Cited
2009
Highly Cited
2009
BackgroundHigh density genetic maps of plants have, nearly without exception, made use of marker datasets containing missing or… Expand
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Highly Cited
2008
Highly Cited
2008
Two types of acquired loss of heterozygosity are possible in cancer: deletions and copy-neutral uniparental disomy (UPD… Expand
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Highly Cited
2008
Highly Cited
2008
BACKGROUND TDP-43 is a major component of the ubiquitinated inclusions that characterise amyotrophic lateral sclerosis (ALS) and… Expand
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Highly Cited
2007
Highly Cited
2007
Comprehensive identification and cataloging of copy number variations (CNVs) is required to provide a complete view of human… Expand
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Highly Cited
2005
Highly Cited
2005
BACKGROUND Human myeloproliferative disorders form a range of clonal haematological malignant diseases, the main members of which… Expand
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