Rare copy number variant analysis in case-control studies using snp array data: a scalable and automated data analysis pipeline. [PDF]
Artaza H +5 more
europepmc +1 more source
Corrigendum: Development of a 50K SNP array for whole-genome analysis and its application in the genetic localization of eggplant (Solanum melongena L.) fruit shape. [PDF]
Yu C +11 more
europepmc +1 more source
Development of a 50K SNP array for whole-genome analysis and its application in the genetic localization of eggplant (Solanum melongena L.) fruit shape. [PDF]
Yu C +11 more
europepmc +1 more source
QTL Mapping of Yield-Related Traits in Tetraploid Wheat Based on Wheat55K SNP Array. [PDF]
Jia Y +11 more
europepmc +1 more source
Mapping of Aegilops speltoides derived leaf rust and stripe rust resistance genes using 35K SNP array. [PDF]
Kaur B +7 more
europepmc +1 more source
Genome-wide QTL mapping for agronomic traits in the winter wheat cultivar Pindong 34 based on 90K SNP array. [PDF]
Zhang L +15 more
europepmc +1 more source
Using the 90K Buffalo SNP Array
The development of the first SNP array (Affymetrix Axiom Buffalo Genotyping Array) officially opened the genomic era for the Buffalo species. More than 123k SNP probes are currently available for the genotyping of 90k SNPs. A total of 1605 individuals were genotyped worldwide within the framework of the International Buffalo Genome Consortium (1376 ...
NICOLAZZI E. L. +13 more
openaire +2 more sources
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Molecular Karyotyping: From Microscope to SNP Arrays
Hormone Research in Paediatrics, 2011Chromosomal rearrangements are an important cause of distinctive and recognizable clinical phenotypes. For many years conventional karyotyping has been a successful tool to detect such chromosomal rearrangements. However, this technique has a limited resolution of 5–10 Mb.
Gijsbers, A.C.J., Ruivenkamp, C.A.L.
openaire +4 more sources
Copy Number and SNP Arrays in Clinical Diagnostics
Annual Review of Genomics and Human Genetics, 2011The ability of chromosome microarray analysis (CMA) to detect submicroscopic genetic abnormalities has revolutionized the clinical diagnostic approach to individuals with intellectual disability, neurobehavioral phenotypes, and congenital malformations.
Christian P, Schaaf +2 more
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