Found 5 results
Filters: Author is Kang, Hyun Min  [Clear All Filters]
McCarthy S, Das S, Kretzschmar W, Delaneau O, Wood AR, Teumer A, Kang HMin, Fuchsberger C, Danecek P, Sharp K et al..  2016.  A reference panel of 64,976 haplotypes for genotype imputation.. Nat Genet. 48(10):1279-83.
Gillies CE, Otto EA, Vega-Warner V, Robertson CC, Sanna-Cherchi S, Gharavi A, Crawford B, Bhimma R, Winkler C, Kang HMin et al..  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.
Sampson MG, Gillies CE, Robertson CC, Crawford B, Vega-Warner V, Otto EA, Kretzler M, Kang HMin.  2016.  Using Population Genetics to Interrogate the Monogenic Nephrotic Syndrome Diagnosis in a Case Cohort.. J Am Soc Nephrol. 27(7):1970-83.
Gillies CE, Robertson CC, Sampson MG, Kang HMin.  2015.  GeneVetter: a web tool for quantitative monogenic assessment of rare diseases.. Bioinformatics. 31(22):3682-4.
Sampson MG, Gillies CE, Ju W, Kretzler M, Kang HMin.  2013.  Gene-level integrated metric of negative selection (GIMS) prioritizes candidate genes for nephrotic syndrome.. PLoS One. 8(11):e81062.