Methods to detect and analyze copy number variations at the genome-wide and locus-specific levels

Publisher： Karger

E-ISSN： 1424-859x|123|1-4|333-342

ISSN： 1424-8581

Source： Cytogenetic and Genome Research, Vol.123, Iss.1-4, 2009-03, pp. : 333-342

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Genome-Wide Mapping Of Copy Number Variations using SNP Arrays

By  

Transfusion Medicine and Hemotherapy, Vol. 36, Iss. 4, 2009-07 ,pp. : 246-251

Karger

Access to resources Recommend Favorite

Rapid Diagnosis of Imprinting Disorders Involving Copy Number Variation and Uniparental Disomy Using Genome-Wide SNP Microarrays

By  

Cytogenetic and Genome Research, Vol. 146, Iss. 1, 2015-07 ,pp. : 9-18

Karger

Access to resources Recommend Favorite

Genome‐wide analysis of DNA copy number alterations and loss of heterozygosity in intracranial germ cell tumors

By  

PEDIATRIC BLOOD & CANCER (ELECTRONIC), Vol. 61, Iss. 4, 2014-04 ,pp. : 593-600

John Wiley & Sons Inc

Access to resources Recommend Favorite

Genome‐wide copy number analyses identified novel cancer genes in hepatocellular carcinoma

By  

HEPATOLOGY, Vol. 54, Iss. 4, 2011-10 ,pp. : 1227-1236

John Wiley & Sons Inc

Access to resources Recommend Favorite

Erratum to: Genome-wide copy number variation association study suggested VPS13B gene for osteoporosis in Caucasians

By Deng F.-Y.   Zhao L.-J.   Pei Y.-F.   Sha B.-Y.   Liu X.-G.   Yan H.   Wang L.   Yang T.-L.   Recker R.   Papasian C.   Deng H.-W.  

Osteoporosis International, Vol. 21, Iss. 8, 2010-08 ,pp. : 1455-1455

Springer Publishing Company

Access to resources Recommend Favorite