Hello, I'm a newbie for the genome sequencing research.
Does anyone have an experience in the human genome alignment with the complete genome and short reads ?
Based on my observations previously mentioned, BLAT was used for aligning the reads to the genomic region.
Can you suggest me more about the software and the computer performance to handle it?
Does anyone have an experience in the human genome alignment with the complete genome and short reads ?
Based on my observations previously mentioned, BLAT was used for aligning the reads to the genomic region.
Can you suggest me more about the software and the computer performance to handle it?
Comment