Dear guru,
The
analyze_diff_expr.pl executes the Trinity-included PtR script to plot a heatmap using euclidean clustering method for gene and sample distance.
PtR -m diffExpr.matrix --log2 --heatmap --min_colSums 0 --min_rowSums 0 --gene_dist euclidean --sample_dist euclidean --sample_cor_matrix --center_rows --save
However, the default clustering method of PtR script for gene and sample distance is Pearson correlation.
May I ask, which clustering method (Euclidean or Pearson correlation) is suitable for RNA-Seq different expression data?
Thank you for your time.
Best regards,
Lim