Hi All
I was intending to map SOLID reads to the viral and bacterial genomes, and was thinking if i can use the same indices as mentioned in the Bfast manual, or do i need to create new ones?
After reading under advanced topics in the manual, i felt that using the same indices might just be stringent. Can someone throw some more light on this?
I was intending to map SOLID reads to the viral and bacterial genomes, and was thinking if i can use the same indices as mentioned in the Bfast manual, or do i need to create new ones?
After reading under advanced topics in the manual, i felt that using the same indices might just be stringent. Can someone throw some more light on this?
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