Targeted human exome enrichment using SeqCap EZ Human Exome Library v2.0 from Roche NimbleGen
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https://www.ncbi.nlm.nih.gov/sra/SRP003451
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资源简介：
Targeted sequencing of the exome has emerged as an efficient method for detection of SNPs and other genomic variations with functional impact. Roche NimbleGen has developed the SeqCap EZ Exome Library v2.0 and gel free protocol for comprehensive and easily automatable investigation of the human exome. The EZ Exome v2.0 design is based on NCBI Reference Sequence (RefSeq) RefGene from UCSC (January 2010), CCDS from NCBI (September 2009), miRBase v.14 (September 2009), and customer inputs. Here we present 7 lanes of Illumina paired-end sequence sets from captures of 2 human HapMap samples: NA19240 (YRI) and NA12762 (CEU).
创建时间：
2013-08-23
