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FGENE.2015.00176
FGENE.2015.00176
http://dx.doi.org/10.3389/FGENE.2015.00176
Integrative analysis of functional genomic annotations and sequencing data to identify rare causal variants via hierarchical modeling.
P356
Q30958077-9BA00118-E4D4-43C3-86AC-03BB22903F1E
P356
FGENE.2015.00176
http://dx.doi.org/10.3389/FGENE.2015.00176