Cell Line Sub Clone Rearrangement Screen
收藏NIAID Data Ecosystem2026-03-10 收录
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资源简介：
Genomic libraries (500 bps) will be generated from total genomic DNA cancer samples and subjected to paired end sequencing on the llumina GA. Paired reads will be mapped to build 37 of the human reference genome to facilitate the generation of genome wide copy number information, and the identification of novel rearranged cancer genes and gene fusions.EGA study EGAS00001000178
创建时间：
2017-07-26
