Because I am so new to DNA sequencing and this type of software, I likely do not have the terminology to explain my question properly. I will post the three files I refer to and hopefully that will make my question more clear.
I have two fasta files containing different genomic sequences of the american eel. I have other data (mergedTables) that correspond to one of the two versions (GCA_001606085.1_ASM160608v1_genomic) of the american eel genome that I have. I would like to use the other version (american_eel_genome_v5), as I have an annotation file that I can use with it in IGB. I've been told that I can use the BLAST algorithm to solve my problem, but I do not understand how as I thought blast was used to find similarities in different species.
Any suggestions would be really helpful. I'm an undergrad working on an independent study.
Aligning chromosome sized pieces is not the best use for BLAST since it does local alignments. You should look into LASTZ (https://github.com/lastz/lastz ) for this type of an application.
Thanks genomax. From what I can tell, LASTZ seems to require some knowledge of coding/running source code, which I am completely unfamiliar with. Is this program intended for use for people with more advanced skills?
If you have managed to run a blastn search on the command line (Can I align two DNA sequences using BLAST from command line? ) then you may be able to use LASTZ. You can find the precompiled binaries for linux on this page: http://hgdownload.soe.ucsc.edu/admin/exe/linux.x86_64/
It is would not be an easy program to use. You may want to find a local collaborator who can assist with this task.