thanks .. how can i perform from R or Excel...
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Hi all,
how can i merge trinscript id from results de novo assembly with trinity . i have givie correlation between Transcript and LncRNA and result too much. so i have remove same isoforms with R. thanks alot
Var1 Var2 Freq
TRINITY_DN17567_c0_g4_i1 Ln.upTRINITY_DN1485_c0_g2_i1 -0.999347304
TRINITY_DN15020_c1_g5_i3 Ln.upTRINITY_DN1485_c0_g2_i1 0.999097516
TRINITY_DN17625_c1_g2_i3 Ln.upTRINITY_DN1485_c0_g2_i1 0.999694545
TRINITY_DN16640_c0_g1_i13 Ln.upTRINITY_DN1485_c0_g2_i1 0.999365559
TRINITY_DN10482_c0_g1_i5 Ln.upTRINITY_DN1485_c0_g2_i1 0.999155939
TRINITY_DN19436_c2_g2_i6 Ln.upTRINITY_DN1454_c0_g1_i1 0.999910259
TRINITY_DN20207_c2_g1_i6 Ln.upTRINITY_DN1454_c0_g1_i1 0.999918395
TRINITY_DN17517_c0_g9_i1 Ln.upTRINITY_DN1454_c0_g1_i1 0.999876373
Trinity provides a script that implements the SuperTranscripts method to collapse all isoforms into one "gene", the script is:
$TRINITY_HOME/Analysis/SuperTranscripts/Trinity_gene_splice_modeler.py
The help page of this script briefly explains the method and contains references to the original paper:
https://github.com/trinityrnaseq/trinityrnaseq/wiki/SuperTranscripts
thanks .. how can i perform from R or Excel...
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