t*d
发帖数: 1290 | 1 MONTREAL (GenomeWeb News) – Analyses of data for nearly 1,100 individuals
assessed through phase 1 of the 1000 Genomes Project have uncovered more
than 40 million genetic variants in the human genome, including almost 30
million SNPs not detected previously.
Overall, the researchers identified some 37.9 million SNPs in the dataset,
including 29.7 million new SNPs. In addition, the team tracked down 3.8
million short indels and 14,000 large deletions. McVean noted that this set
represents highly conservative indels and deletions taken through integrated
analyses. | A********2
发帖数: 107 | 2 How about duplications and inversions? |
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