I have completed Trinity de novo assembly for a worm species. The k-mer that I used was 25. Then, I have had too many genes and transcripts. How can I remove the duplications of the same transcripts?
>c4_g1_i1 len=584 path=[53:0-583] >c5_g1_i1 len=221 path=[47:0-166 213:167-220] >c6_g1_i1 len=223 path=[735:0-15 737:16-222] Total trinity 'genes': 29340 Total trinity transcripts: 37318 Total assembled bases: 21926265