I would like to align reads to the genome of the Macaca fascicularis monkey.
Until now, the genomes I worked with appeared in the Illumina iGenomes page:


And so I had the WholeGenomeFasta/genome.fa file to work with (from which I created the STAR index etc).
However, there is no iGenome for Macaca fascicularis and so I downloaded the fasta files from the Ensembl site, under "Download DNA Sequences":


Which are all the files here:


I'd like to create a single genome.fa file that is similar to the one from iGenomes. My question is: should this be done simply by concatenating the *dna.primary_assembly fasta files?

Thanks a lot! 🙂


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