Whole genome amplification with SurePlex results in better copy number alteration detection using sequencing data compared to the MALBAC method-Reference-Cited by-同舟云学术

Whole genome amplification with SurePlex results in better copy number alteration detection using sequencing data compared to the MALBAC method

Published:2015-06-30 Issue:1 Volume:5 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Deleye Lieselot,Coninck Dieter De,Christodoulou Christodoulos,Sante Tom,Dheedene Annelies,Heindryckx Björn,Abbeel Etienne Van den,Sutter Petra De,Menten Björn,Deforce Dieter,Nieuwerburgh Filip Van

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep11711.pdf

Reference21 articles.

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2. Fiorentino, F. et al. Development and validation of a next-generation sequencing-based protocol for 24-chromosome aneuploidy screening of embryos. Fertility and sterility 101, 1375–1382, 10.1016/j.fertnstert.2014.01.051 (2014).

3. Treff, N. R., Su, J., Tao, X., Levy, B. & Scott, R. T., Jr. Accurate single cell 24 chromosome aneuploidy screening using whole genome amplification and single nucleotide polymorphism microarrays. Fertility and sterility 94, 2017–2021, 10.1016/j.fertnstert.2010.01.052 (2010).

4. Wells, D. et al. Clinical utilisation of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantation. Journal of medical genetics 51, 553–562, 10.1136/jmedgenet-2014-102497 (2014).

5. Van Loo, P. & Voet, T. Single cell analysis of cancer genomes. Current opinion in genetics & development 24, 82–91, 10.1016/j.gde.2013.12.004 (2014).

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