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tarSVM: Improving the accuracy of variant calls derived from microfluidic PCR-based targeted next generation sequencing using a support vector machine., , , , , , , , , and 1 other author(s). BMC Bioinformatics, (2016)Comparing variant calling algorithms for target-exon sequencing in a large sample., , , , , , , and . BMC Bioinformatics, (2015)Unified representation of genetic variants., , and . Bioinformatics, 31 (13): 2202-2204 (2015)Imputation of coding variants in African Americans: better performance using data from the exome sequencing project., , , , , , , , , and 25 other author(s). Bioinformatics, 29 (21): 2744-2749 (2013)Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease., , , , , , , , , and 17 other author(s). NeuroImage, 51 (2): 542-554 (2010)EMINIM: An Adaptive and Memory-Efficient Algorithm for Genotype Imputation., , and . Journal of Computational Biology, 17 (3): 547-560 (2010)emeraLD: rapid linkage disequilibrium estimation with massive datasets., , , , , and . Bioinformatics, 35 (1): 164-166 (2019)GeneVetter: a web tool for quantitative monogenic assessment of rare diseases., , , and . Bioinformatics, 31 (22): 3682-3684 (2015)Mixed-model coexpression: calculating gene coexpression while accounting for expression heterogeneity., , , and . Bioinformatics ISMB/ECCB, 27 (13): 288-294 (2011)An Adaptive and Memory Efficient Algorithm for Genotype Imputation., , , and . RECOMB, volume 5541 of Lecture Notes in Computer Science, page 482-495. Springer, (2009)