Found 5 results
Filters: Author is Kang, Hyun Min [Clear All Filters]
A reference panel of 64,976 haplotypes for genotype imputation.. Nat Genet. 48(10):1279-83.
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2016. tarSVM: Improving the accuracy of variant calls derived from microfluidic PCR-based targeted next generation sequencing using a support vector machine.. BMC Bioinformatics. 17(1):233.
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2016. Using Population Genetics to Interrogate the Monogenic Nephrotic Syndrome Diagnosis in a Case Cohort.. J Am Soc Nephrol. 27(7):1970-83.
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2016. GeneVetter: a web tool for quantitative monogenic assessment of rare diseases.. Bioinformatics. 31(22):3682-4.
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