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8-chip high-resolution aCGH experiment NA15510 vs. NA18505

GSE9002 Homo sapiens Genome variation profiling by genome tiling array 8 samples Submitted 2007/09/28 Platform GPL5821Platform GPL5816Platform GPL5819Platform GPL5814Platform GPL5820Platform GPL5817Platform GPL5815Platform GPL5818
Summary
We introduce high-throughput and massive paired-end mapping (PEM), a large-scale genome sequencing method to identify SVs 3 kb or larger that combines the rescue and capture of paired-ends of 3 kb fragments, massive 454 Sequencing, and a computational approach to map DNA reads onto a reference genome. PEM was used to map SVs in an African and putatively European individual and identified shared and divergent SVs relative to the reference genome. Overall, we fine-mapped more than 1000 SVs and documented that the number of SVs among humans is much larger than initially hypothesized; many of the SVs potentially affect gene function. The breakpoint junction sequences of more than 200 SVs were deduced with a novel pooling strategy and computational analysis. Array-CGH was used for validation. Keywords: array CGH
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Also filed as BioProject PRJNA102481. Searching any of these in the dataset finder brings you back here.

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