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any high-throughput method is potentially
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appropriate
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genome-scale vs. "candidate genes" scale. cost of
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screening for 500,000 SNP's will be impractical
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for most purposes--may benefit from extremely
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small feature size (SNR not as important since
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only interested in 0-1-2)
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how to haplotype without separating chromosomes,
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doing separate allelic amplification?
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