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reciprocal blast
Jiali Yu edited this page Jun 2, 2020
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Analysis is stored in <your_project_directory>
- peach protein fasta sequences download from phytozome
- cherry protein fasta sequences download from GDR
spack load [email protected]
makeblastdb -in protein_fasta_file -dbtype prot
-in
input file.
-dbtype
input file format (nucleotide sequences as nucl, protein sequences as prot).
spack load [email protected]
blastp \
-query <peach_protein_sequence.fasta> \
-db <cherry_protein_sequence.fasta> \
-out <your_output_file.txt> \
-evalue 1e-5 \
-outfmt 6 \
-max_target_seqs 1 \
-num_threads 10
-quary
input sequences.
-db
reference sequences.
-out
output file.
-evalue
evalue cutoff.
outfmt
output format. 6 means a tab separate format.
-max_target_seqs
keep one hit (one of the best hit).
-num_threads
number of cores will use to run this program.
Use cherry sequences as query and peach sequences as reference. Run the same blastp command as above.
There is a python script we can use. We will try it once we get there.