Closed Simon602 closed 5 years ago
HI @Simon602 ,
Regarding your first question, the mRNA specificity actually starts at ~0 but the y-axis limits is zoomed to 0,5->1.
according to the curves which method is better, training with lncRNA.fasta or --mode=shuffle ?
It really depends on the confidence you have in your lncRNA training file. If your are not sure about their robustness, you can indeed use the shuffle
method (which performs better than intergenic
in our analysis)
Bw,
Thomas
Dear All
in the codpot.pl, I used the lncRNAs sequence to train the algorithm but the in the graph ROC curves there is a shifting in mRNA specificity curves when I launched it with -l flag to train algorithm with lncRNAs fasta sequence compare to --mode=shuffle or intergenic flags, why coding probability for mRNA specificity curve started at 0.2 ? according to the curves which method is better, training with lncRNA.fasta or --mode=shuffle ? Thanks