hum0036 Release Note

Research IDRelease DateType of Data
hum0036.v1 2015/08/01 NGS (Exome)



gDNAs extracted from EBV-transformed lymphoblastoid cell lines (LCL) derived from two HapMap-JPT samples obtained from Coriell were used for the whole exome sequencing (fastq files). DNA fragments containing whole coding exons were concentrated using SeqCap EZ Human Exome Library v3.0 (Roche/NimbleGen), Illumina [Nextera Rapid Capture Exome v1.2 (Illumina), SureSelect XT Human All Exon v5 (Agilent) or SureSelect QXT Human All Exon v5 (Agilent) and multiplex sequence was performed with the Illumina HiSeq 2500 sequencer (161 bp x 2, Paired-end).