Below is the summary of my findings:
1.The genome was sequenced to 36-fold average coverage using massively parallel sequencing technology.
2. When aligned the short reads onto the NCBI human reference genome to 99.97% coverage, and guided by the reference genome, we used uniquely mapped reads to assemble a high-quality consensus sequence for 92% of the Asian individual’s genome.
Can anybody list the main findings from the "The diploid genome sequence of an Asian individual" research?
Thanks a lot
1.The genome was sequenced to 36-fold average coverage using massively parallel sequencing technology.
2. When aligned the short reads onto the NCBI human reference genome to 99.97% coverage, and guided by the reference genome, we used uniquely mapped reads to assemble a high-quality consensus sequence for 92% of the Asian individual’s genome.
Can anybody list the main findings from the "The diploid genome sequence of an Asian individual" research?
Thanks a lot
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