I’d like to sequence the tumor sample that material is very limited amount. My goal is to find a structural variant like large inversion and deletion (translocation if possible) in a single tumor cell. The problem is that whole genome amplification by Multiple Displacement Amplification will produce many inversion false positives as this article says;
“Jiao et al., Structural Alterations from Multiple Displacement Amplification of a Human Genome Revealed by Mate-Pair Sequencing” (http://www.plosone.org/article/info%...l.pone.0022250)
Do you know any methods that are capable to amplify whole genomes with minimum conformational change in the sample genome?
Or shouldn’t I use the amplification method for structural analysis of genome?
I understand amplification bias is inevitable is these kind of technologies.
Best,
Ken
“Jiao et al., Structural Alterations from Multiple Displacement Amplification of a Human Genome Revealed by Mate-Pair Sequencing” (http://www.plosone.org/article/info%...l.pone.0022250)
Do you know any methods that are capable to amplify whole genomes with minimum conformational change in the sample genome?
Or shouldn’t I use the amplification method for structural analysis of genome?
I understand amplification bias is inevitable is these kind of technologies.
Best,
Ken
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