When I BLAST two sequences with a mismatch at position 3 using NCBI's servers and selecting "somewhat similar sequences (blastn)" as an option, I get a report that begins at base 1. However, when I use the command line BLAST+ to perform the same alignment, I get a report that begins at base 4 after the mismatch. How can I modify the command line version to mimic what NCBI's servers are doing?
blastn -query ref.fa -subject clone.fa
I noticed that NCBI is using BLASTN 2.2.31+ while my current version is 2.2.30+. Does that make all the difference?