single nucleotide*

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SNP discovery via 454 transcriptome sequencing
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Integrating common and rare genetic variation in diverse human populations
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A genome-wide survey of the prevalence and evolutionary forces acting on human nonsense SNPs
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National Center for Biotechnology Information NCBI NLM MEDLINE pubmed abstract nih national institutes of health national library of medicine research support non-u.s. gov't u.s. gov't non-p.h.s. Sequence Analysis genome Base Sequence Molecular Sequence Data Polymorphism DNA / methods* scott j emrich w brad barbazuk