KRGDB genomic database
Contributed genomic preprocessing, variant analysis, and annotation for KRGDB.
At a public health research institute, I contributed to genomic analysis from January 2014 to March 2017. My work prepared sequence data for analysis and connected variant frequencies with public-database annotations.
Analysis work
I used Linux, Python, and Samtools for preprocessing and analysis, examined variant frequencies within and between populations, and annotated variants using public databases.
Research output
KRGDB is a variant database based on whole-genome sequencing of 1,722 Koreans. The associated paper was published in 2020; my analysis work took place in 2014–2017.