Whole Genome Amplification

WGA References

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Publications:
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Title Author / Journal
Evaluation of whole genome amplification protocols for array and oligonucleotide CGH. Hittelman A, et al.Diagn Mol Pathol. 2007 Dec; 16(4), 198-206.
A non-invasive test for prenatal diagnosis based on fetal DNA present in maternal blood: a preliminary study. Dhallan, R. et al.
Lancet 2007 Feb 10; 369(9560), 474-81.
Whole genome amplification and genetic analysis after extraction of proteins from dried blood spots. Hollegaard, M. V. et al.
Clin. Chem. 2007 Jun; 53(6), 1161-2.
Single-cell isolation from cell suspensions and whole genome amplification from single cells to provide templates for CGH analysis. Geigl, J. B. et al.
Nat. Protoc. 2007; 2(12), 3173-84.
Genome-scale ChIP-chip analysis using 10,000 human cells. (link not available) Acevedo, L. G. et al.
BioTechniques 2007 Dec; 43(6), 791-7.
A novel role for the Aurora B kinase in epigenetic marking of silent chromatin in differentiated postmitotic cells. Sabbattini P. et al.
EMBO J. 2007 Nov 14; 26(22), 4657-69.
Genome-Wide Analysis of KAP1 Binding Suggests Autoregulation of KRAB-ZNFs. O'geen, H. et al.
PLoS Genet. 2007 Jun 1; 3(6), e89.
Whole genome amplification on DNA from filter paper blood spot samples: an evaluation of selected systems. Sorenson, K. M. et al.
Genet. Test. 2007 Spring; 11(1), 65-75.
High resolution array-CGH analysis of single cells. Fiegler, H. et al.
Nucleic Acids Res. 35(3), e15 (2007).
Comparison of sample preparation methods for ChIP-chip assays. Farnham, P. J. et al.
Biotechniques 41(5), 577-770 (2006).
Application of array CGH on archival formalin-fixed paraffin embedded tissues including small numbers of microdissected cells. Johnson, N. A. et al.
Lab. Invest. 86(9), 968-78 (2006).
Variants in the gene encoding C3 are associated with asthma and related phenotypes among African Caribbean families. Barnes, K. C. et al.
Genes Immun. 7(1), 27-35(Jan 2006).
Polymorphisms in the novel gene acyloxyacyl hydroxylase (AOAH) are associated with asthma and associated phenotypes. Barnes, K. C. et al.
J. Allergy. Clin. Immun. 218(1), 70-77(2006).
Array CGH using whole genome amplification of fresh-frozen and formalin-fixed, paraffin-embedded tumor DNA. Little, S. E. et al.
Genomics Oct. 31, 2005.
Two methods of whole-genome amplification enable accurate genotyping across a 2320-SNP linkage panel. Barker, D. L. et al.
Genome Res. 14, 901-907 (2004).
Chromosome paints from single copies of chromosomes. Gribble, S. et al.
Chromosome Res. 12(2), 143-51(2004).
Applications of combined DNA microarray and chromosome sorting technologies. Gribble, S. et al.
Chromosome Res. 12(1), 35-43(2004).
An Automated Hydrodynamic Process for Controlled, Unbiased DNA Shearing. Thorstenson, Y. R. et al.
Genome Res. 8, 848-855 (1998).
Comparing Whole-Genome Amplification Methods and Sources of Biological Samples for Single-Nucleotide Polymorphism Genotyping. Park, J. W. et al.
Clin. Chem. 51 (8), 1520-1523 (2004).