Entering edit mode
8.8 years ago
loly.pearl86
▴
30
Hi All,
Can some one explain to me how can I generate the longest and shortest contigs length from this trinity assembly summary:
################################
## Counts of transcripts, etc.
################################
Total trinity 'genes': 306290
Total trinity transcripts: 369174
Percent GC: 48.47
########################################
Stats based on ALL transcript contigs:
########################################
Contig N10: 5172
Contig N20: 3581
Contig N30: 2517
Contig N40: 1717
Contig N50: 1095
Median contig length: 333
Average contig: 659.77
Total assembled bases: 243568232
#####################################################
## Stats based on ONLY LONGEST ISOFORM per 'GENE':
#####################################################
Contig N10: 4276
Contig N20: 2665
Contig N30: 1655
Contig N40: 1006
Contig N50: 664
Median contig length: 313
Average contig: 540.34
Total assembled bases: 165499422
Thanks
Thanks for u quick replay but I am not sure where can I run this script??! look like for Rstudio !! I am working on linux using (Putty) SSH. So can I run this script on SHH command line? If no, then can you please suggest to me other way which I can use it in linux
thanks
Yes. You can do it from the command line. Just move to the folder where your fasta file is located, and copy paste the command replacing
file
with your file name.Thanks I did run it
its give me this result: shortest = 0 that is all !!
Sorry, I'd a little mistake. Can you try now?
Thanks its work now. But the results its unusual
I have 5 assembled samples , and the outcome of the script was
sample 1: shortest 1 longest 14357
Sample 2 , 3 ,4: shortest= 7 longest= 9
Sample 5 shortest=6 longest =89 Is this mean any things like my samples quality are poor or low quality??!!!
thanks