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Transcripts were ordered by hierarchical clustering (complete linkage).
All eight SNPs were in almost complete linkage disequilibrium.
The two polymorphisms were in complete linkage disequilibrium.
The plot was drawn using hierarchical cluster analysis with complete linkage.
Transcripts were ordered by hierarchical clustering (complete linkage) with Nlgn1−/− fold change taken as a reference.
The strongest association was seen for rs2395029[G], a marker in complete linkage disequilibrium with HLA-B*5701 HLA-B*5701
For hierarchical cluster analysis, the complete linkage method and the Euclidean distance were used.
Clusters were built using a similarity threshold of 0.7 with a complete linkage algorithm.
Hierarchical clustering was performed using complete linkage and euclidean distance.
Both datasets were clustered hierarchically, using complete linkage clustering.
Data were median-centered by gene and clustering was based on centered correlation and complete linkage.
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