Do you guys have any idea which NGS platform is the most suitable for doing the whole genome rearrangement project ?
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Any paired-end or long read platform will be adequate.
Solexa, SOLiD and 454 will all work for this type of project, and you should consider how much you're planning to sequence and what resources are available to you to decide which to use.Mendelian Disorder: A blogshare of random useful information for general public consumption. [Blog]
Breakway: A Program to Identify Structural Variations in Genomic Data [Website] [Forum Post]
Projects: U87MG whole genome sequence [Website] [Paper]
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