Integrating multiple genomic data to predict disease-causing nonsynonymous single nucleotide variants in exome sequencing studies (Q30781978)
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English | Integrating multiple genomic data to predict disease-causing nonsynonymous single nucleotide variants in exome sequencing studies |
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Integrating multiple genomic data to predict disease-causing nonsynonymous single nucleotide variants in exome sequencing studies (English)
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Jiaxin Wu
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Yanda Li
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20 March 2014
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e1004237
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20 March 2014
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