It works when I tried e-value cutoff of 13. The output is as below:
BLASTN 2.6.0+
Reference: Stephen F. Altschul, Thomas L. Madden, Alejandro A.
Schaffer, Jinghui Zhang, Zheng Zhang, Webb Miller, and David J.
Lipman (1997), "Gapped BLAST and PSI-BLAST: a new generation of
protein database search programs", Nucleic Acids Res. 25:3389-3402.
Database: db.fa
32 sequences; 704 total letters
Query= AB011515
Length=630
Score E
Sequences producing significant alignments: (Bits) Value
DB_26 14.4 12
DB_18 14.4 12
DB_10 14.4 12
DB_02 14.4 12
DB_32 14.4 12
DB_31 14.4 12
DB_30 14.4 12
DB_29 14.4 12
DB_28 14.4 12
DB_27 14.4 12
DB_25 14.4 12
DB_24 14.4 12
I will adjust e-value in this case. Thanks a lot for your help!
let me first point out that this a very old version for blast you're using (we're at 2.10.0 for the moment)
Do you get any output when running the 'normal' blastn? (blastn-short actually points to short input query's and not short sequences in the DB)
Can you post the output of the
makeblastdbcmd? moreover, for the version 2.2.18 the command to use to format a blastdb wasformatdb(and notmakeblastdb)My apologies. It was version 2.6.0 not 2.2.18. I will correct it. It produces no hit using normal
blastnas well.The
makeblastdboutput is as below:OK, looks all fine.
Can you post what the hits look like (in the second try you mention)?
Are the 26 sequences a subpart of the 32 or are they different sequences? Could it be there simply are not hits?
The original 32 sequences are different. For simplicity, I created a database of 32 duplicates as
db.faand 26 duplicates fordb.partial.fa. Therefore, fordb.fa, it looks like this (As you can see, they are all the same):and db.partial.fa is from
DB_01 to DB_26ofdb.fa.Please find below the blast output: using
db.fausing
db.partial.faCan I, on the side, ask what the goal of all this is? So far it is making little (biological) sense to me :/
@lieven.sterck. Nothing much special. I was trying to match sequences with different composition of primers and realised that I could not do it with more primer sequences and had not clue why.