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本文引用的文献

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Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptome.
Science. 2015 May 8;348(6235):666-9. doi: 10.1126/science.1261877.
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Human genomics. The human transcriptome across tissues and individuals.
Science. 2015 May 8;348(6235):660-5. doi: 10.1126/science.aaa0355.
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Gene-gene and gene-environment interactions detected by transcriptome sequence analysis in twins.
Nat Genet. 2015 Jan;47(1):88-91. doi: 10.1038/ng.3162. Epub 2014 Dec 1.
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Clinical interpretation and implications of whole-genome sequencing.
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Bayesian model selection in complex linear systems, as illustrated in genetic association studies.
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The NHGRI GWAS Catalog, a curated resource of SNP-trait associations.
Nucleic Acids Res. 2014 Jan;42(Database issue):D1001-6. doi: 10.1093/nar/gkt1229. Epub 2013 Dec 6.
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Characterizing the genetic basis of transcriptome diversity through RNA-sequencing of 922 individuals.
Genome Res. 2014 Jan;24(1):14-24. doi: 10.1101/gr.155192.113. Epub 2013 Oct 3.
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Integrative annotation of variants from 1092 humans: application to cancer genomics.
Science. 2013 Oct 4;342(6154):1235587. doi: 10.1126/science.1235587.
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Systematic identification of trans eQTLs as putative drivers of known disease associations.
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