Computational methods for identification of recurrent copy number alteration patterns by array CGH

Publisher： Karger

E-ISSN： 1424-859x|123|1-4|343-351

ISSN： 1424-8581

Source： Cytogenetic and Genome Research, Vol.123, Iss.1-4, 2009-03, pp. : 343-351

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

Benign copy number changes in clinical cytogenetic diagnostics by array CGH

By  

Cytogenetic and Genome Research, Vol. 123, Iss. 1-4, 2009-03 ,pp. : 94-101

Karger

Access to resources Recommend Favorite

Gene copy number analysis in malignant pleural mesothelioma using oligonucleotide array CGH

By  

Cytogenetic and Genome Research, Vol. 119, Iss. 1-2, 2007-12 ,pp. : 46-52

Karger

Access to resources Recommend Favorite

Diagnosis of fetal submicroscopic chromosomal abnormalities in failed array CGH samples: copy number by sequencing as an alternative to microarrays for invasive fetal testing

By  

ULTRASOUND IN OBSTETRICS & GYNECOLOGY, Vol. 45, Iss. 4, 2015-04 ,pp. : 394-401

John Wiley & Sons Inc

Access to resources Recommend Favorite

Consistent copy number changes and recurrent PRKAR1A mutations distinguish Melanotic Schwannomas from Melanomas: SNP‐array and next generation sequencing analysis

By  

GENES, CHROMOSOMES AND CANCER, Vol. 54, Iss. 8, 2015-08 ,pp. : 463-471

John Wiley & Sons Inc

Access to resources Recommend Favorite

Identification of a characteristic copy number alteration profile by high‐resolution single nucleotide polymorphism arrays associated with metastatic sporadic colorectal cancer

By  

CANCER, Vol. 120, Iss. 13, 2014-07 ,pp. : 1948-1959

John Wiley & Sons Inc

Access to resources Recommend Favorite