t*d
2 楼
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.
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
4 楼
How about duplications and inversions?
相关阅读
Paper help again, 10 baozi as acknowledgement说一下我了解的法国研究系统。请推荐一种电子阅读器巴求篇文献 (Cell Adhesion & Migration)真想找个生物博后做男朋友 (转载)最近有人带poster上飞机吗?谁推荐个可以用于cell treatment的lysosomal degradation inhibitor说说我今天的经历,和组里的一个女同学没有大paper的CSHL APs: TO 大家看一看我LG这样还有希望走学术paper收了 发些包子吧Tough Lessons From Golden Rice 不错的转基因故事就是不知道怎么写文章,请过来人指点!也鲁的研究科学家(RESEARCH SCIENTIST)工资多高?【讨论】中英文专业术语,大家都学么 (转载)Lipid phosphatase有人用过flow cytometry 检测HCV protein的抗体吗?3.9-3.12 会议Stand Up for University of California请教有关在线转录因子预测程序TESS的问题Gene Expression的paper到底有多可信