Copy number analysis by low coverage whole genome sequencing using ultra low-input DNA from formalin-fixed paraffin embedded tumor tissue-Reference-Cited by-同舟云学术

Copy number analysis by low coverage whole genome sequencing using ultra low-input DNA from formalin-fixed paraffin embedded tumor tissue

Published:2016-11-15 Issue:1 Volume:8 Page:
ISSN:1756-994X
Container-title:Genome Medicine
language:en
Short-container-title:Genome Med

Author:

Kader Tanjina,Goode David L.,Wong Stephen Q.,Connaughton Jacquie,Rowley Simone M.,Devereux Lisa,Byrne David,Fox Stephen B.,Mir Arnau Gisela,Tothill Richard W.,Campbell Ian G.,Gorringe Kylie L.

Funder

Australian National Health and Medical Research Council

National Breast Cancer Foundation

Peter MacCallum Cancer Foundation

NHMRC Early Career Fellowship

Melbourne International Research Scholarship

Melbourne International Fee Remission Scholarship

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics,Molecular Biology,Molecular Medicine

Link

http://link.springer.com/content/pdf/10.1186/s13073-016-0375-z.pdf

Reference25 articles.

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3. Kallioniemi A, Kallioniemi O, Sudar D, Rutovitz D, Gray J, Waldman F, et al. Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science. 1992;258(5083):818–21.

4. Wang Y, Carlton VE, Karlin-Neumann G, Sapolsky R, Zhang L, Moorhead M, et al. High quality copy number and genotype data from FFPE samples using Molecular Inversion Probe (MIP) microarrays. BMC Med Genomics. 2009;2:8.

5. Wang Y, Moorhead M, Karlin-Neumann G, Wang NJ, Ireland J, Lin S, et al. Analysis of molecular inversion probe performance for allele copy number determination. Genome Biol. 2007;8(11):R246.

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