how to remove redundant sequences from assembled transcripts
I have assembled the raw reads successfully. Now I want to remove any redundant transcripts from my assembly if there is any. Which too is best suited for it.
Thanks
• 2,229 views
•
link
updated
by
urjaswita
•
written
by
majeedaasim •
•
written
by
majeedaasim •
1 answer
Log in to answer this question.
More posts like this
-
Tools for Reference-Guided Assembly Using Nanopore Sequencing Reads
written by pratikshaadagale39722 •
-
Running SNIPPY on assembled genomes (calling variations from assembled genomes)
written by Kausik •
-
Extracting transcripts from whole-transcriptome libraries
written by julianneradford •
-
De novo transcriptome assembly produce too many transcripts
written by 21afiq •
-
how to filter specific sequences from my assembled transcripts
written by majeedaasim •
-
De novo assembled transcript mapping to genome scaffold
written by Bioinfonext
-
to separate assembled reads on the basis of size.
written by faizansaleem1992 •
-
transcriptome assembly redundant removal
written by 402374688 •
-
Reg - Seperate unique and redundant reads from raw fastq file.
written by vishweshwaransridhar •
-
Fast Pairwise Alignments Of Assembled Transcripts
written by James Smith •
Is your question answered by this: How to cluster transcripts assembled using TRINITY into unigene after blast?
Hello majeedaasim!
Questions similar to yours can already be found at:
We have closed your question to allow us to keep similar content in the same thread.
If you disagree with this please tell us why in a reply below. We'll be happy to talk about it.
Cheers!