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BMC Medical Genomics|December 17, 2011
Batch effect correction for genome-wide methylation data with Illumina Infinium platformZhifu Sun, High Seng Chai, Yanhong Wu, et al.Journal of the American Medical Informatics Association : JAMIA|January 18, 2012
Impact of data fragmentation across healthcare centers on the accuracy of a high-throughput clinical phenotyping algorithm for specifying subjects with type 2 diabetes mellitusWei-Qi Wei, Cynthia L Leibson, Jeanine E Ransom, et al.Hypertension (Dallas, Tex. : 1979)|July 2, 2008
Genomic association analysis suggests chromosome 12 locus influencing antihypertensive response to thiazide diureticStephen T Turner, Kent R Bailey, Brooke L Fridley, et al.Circulation. Cardiovascular Genetics|October 4, 2011
Homozygosity mapping and exome sequencing reveal GATAD1 mutation in autosomal recessive dilated cardiomyopathyJeanne L Theis, Katharine M Sharpe, Martha E Matsumoto, et al.Diabetes|March 15, 2012
Concordance of changes in metabolic pathways based on plasma metabolomics and skeletal muscle transcriptomics in type 1 diabetesTumpa Dutta, High Seng Chai, Lawrence E Ward, et al.Nucleic Acids Research|May 31, 2011
A novel bioinformatics pipeline for identification and characterization of fusion transcripts in breast cancer and normal cell linesYan W Asmann, Asif Hossain, Brian M Necela, et al.Bioinformatics (Oxford, England)|November 18, 2011
TREAT: a bioinformatics tool for variant annotations and visualizations in targeted and exome sequencing dataYan W Asmann, Sumit Middha, Asif Hossain, et al.Mayo Clinic Proceedings|June 8, 2011
Mayo Genome Consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levelsSuzette J Bielinski, High Seng Chai, Jyotishman Pathak, et al.Frontiers in Oncology|June 2, 2012
Deep Sequence Analysis of Non-Small Cell Lung Cancer: Integrated Analysis of Gene Expression, Alternative Splicing, and Single Nucleotide Variations in Lung Adenocarcinomas with and without Oncogenic KRAS MutationsKrishna R Kalari, David Rossell, Brian M Necela, et al.Neurology. Genetics|April 12, 2016
Late-onset Alzheimer disease risk variants mark brain regulatory lociMariet Allen, Michaela Kachadoorian, Minerva M Carrasquillo, et al.Pageof 3