Newborn variation data of Lithuanians
收藏Mendeley Data2025-01-01 更新2026-04-09 收录
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资源简介：
Whole genome sequencing variation data of newborns with Lenticulostriate vasculopathy (n=6) and control group newborns (n=19).
WGS and quality control analysis was completed by CeGaT company, located in Tubingen, Germany. 100 ng of genomic DNA was sequenced paired–end using Illumina NovaSeqTM 6000 Sequencing System at coverage of 26.88–61.38× (an average of 36.27×). Analysis of sequenced genomes was performed using the Illumina DRAGEN platform (v3.6.4). Reads were mapped to the reference human genome hg19. The quality of the FASTQ files was assured using FastQC software.
创建时间：
2025-01-01
