Direct identification of the causal gene for the family by exome sequencing.
收藏NIAID Data Ecosystem2026-03-08 收录
下载链接：
https://figshare.com/articles/dataset/_Direct_identification_of_the_causal_gene_for_the_family_by_exome_sequencing_/1516964
下载链接
链接失效反馈官方服务：
资源简介：
Rows show the stepwise screening of the total non-synonymous/splice acceptor and donor site/insertions or deletions (NS/SS/Indel) to exclude those found in dbSNP129, the eight HapMap exomes, the dbSNP 1000 genomes, or all. Columns indicate the the number of NS/SS/Indel variants observed in each affected individual (Columns 2–3) or both affected individuals (Columns 4) following exclusion criteria.
Direct identification of the causal gene for the family by exome sequencing.
创建时间：
2015-08-21
