Open LorenaDerezanin opened 6 years ago
I hope @mmatschiner can answer this one...
No, but @martinmalmstrom might?
Hi again gents,
it seems it's been awhile since you've been working on this script :D so I wanted to suggest a somewhat easier solution if you don't mind, and that is to please send me an example of the output file in the following step if possible:
for f in ORFs/*; do \
extract_fasta $f \
>> ${f%_splitted_utg_reads_???}"_merged_ORFs" \
; done
cd ORFs
mkdir ORFs_FASTA
mv *_ORFs ORFs_FASTA
echo "6) Utg-ORFs predicted and parsed" \
>> ~/Progressreports_2015/Progress_$FISH
so I could perhaps reconstruct the extract_fasta
command and write it on my own based on one of the output files with the "_merged_ORFs" suffix.
Thank you for your effort! Lorena
Hello Lex, I'm adjusting your Gene_mining.slurm script from
S19_genome_mining_and_gene_identification/scripts
to mine mammal immune genes but I got stuck at theextract_fasta
step. I assume this command merges all the unitig reads(containing predicted ORFs) with the same prefix in the file name, but I was wondering how it merges unitig IDs. Isextract_fasta
a part of some particular package or you maybe have it stuck somewhere? I would appreciate a lot if you could share that piece of code.Thank you! Lorena