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Items: 9

1.

A classification model for distinguishing copy number variants from cancer-related alterations.

Ostrovnaya I, Nanjangud G, Olshen AB.

BMC Bioinformatics. 2010 Jun 2;11:297. doi: 10.1186/1471-2105-11-297.

2.

Copy number alterations and copy number variation in cancer: close encounters of the bad kind.

Speleman F, Kumps C, Buysse K, Poppe B, Menten B, De Preter K.

Cytogenet Genome Res. 2008;123(1-4):176-82. doi: 10.1159/000184706. Epub 2009 Mar 11. Review.

PMID:
19287153
3.

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

Shah SP.

Cytogenet Genome Res. 2008;123(1-4):343-51. doi: 10.1159/000184726. Epub 2009 Mar 11. Review.

PMID:
19287173
4.

Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome.

Zhang J, Feuk L, Duggan GE, Khaja R, Scherer SW.

Cytogenet Genome Res. 2006;115(3-4):205-14. Review.

PMID:
17124402
5.

Array comparative genomic hybridization copy number profiling: a new tool for translational research in solid malignancies.

Costa JL, Meijer G, Ylstra B, Caldas C.

Semin Radiat Oncol. 2008 Apr;18(2):98-104. doi: 10.1016/j.semradonc.2007.10.005. Review.

PMID:
18314064
6.

Copy number variations and cancer susceptibility.

Shlien A, Malkin D.

Curr Opin Oncol. 2010 Jan;22(1):55-63. doi: 10.1097/CCO.0b013e328333dca4. Review. Retraction in: Curr Opin Oncol. 2016 Sep;28(5):453.

PMID:
19952747
7.

[Analysis of genomic copy number alterations of malignant lymphomas and its application for diagnosis].

Tagawa H.

Gan To Kagaku Ryoho. 2007 Jul;34(7):975-82. Review. Japanese.

PMID:
17637530
8.

Characterisation of hairy cell leukaemia by tiling resolution array-based comparative genome hybridisation: a series of 13 cases and review of the literature.

Nordgren A, Corcoran M, Sääf A, Bremer A, Kluin-Nelemans HC, Schoumans J, Grandér D.

Eur J Haematol. 2010 Jan 1;84(1):17-25. doi: 10.1111/j.1600-0609.2009.01334.x. Review.

PMID:
19682064
9.

Large-scale copy number variants (CNVs) detected in different ethnic human populations.

Takahashi N, Satoh Y, Kodaira M, Katayama H.

Cytogenet Genome Res. 2008;123(1-4):224-33. doi: 10.1159/000184712. Epub 2009 Mar 11. Review.

PMID:
19287159

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