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Human Genome Variation: Linking Genotypes to Clinical Phenotypes - Session Introduction.

, , and . Pacific Symposium on Biocomputing, page 3-5. (2001)

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On the Power to Detect SNP/Phenotype Association in Candidate Quantitative Trait Loci Genomic Regions: A Simulation Study., , and . Pacific Symposium on Biocomputing, page 478-489. (2003)Session Introduction., , , , , and . Pacific Symposium on Biocomputing, page 8-9. (2015)A report on the 2009 SIG on short read sequencing and algorithms (Short-SIG)., , , and . Bioinformatics, 25 (21): 2863-2864 (2009)Human Genome Variation: Haplotypes, Linkage Disequilibrium, and Populations - Session Introduction., , and . Pacific Symposium on Biocomputing, page 463-465. (2003)A Tool for Selecting SNPs for Association Studies Based on Observed Linkage Disequilibrium Patterns., , and . Pacific Symposium on Biocomputing, page 487-498. World Scientific, (2006)Session Introduction., , , and . Pacific Symposium on Biocomputing, page 451-453. World Scientific, (2006)Session Introduction., , and . Pacific Symposium on Biocomputing, page 89-92. World Scientific, (2004)Session Introduction., , and . Pacific Symposium on Biocomputing, page 74-75. World Scientific Publishing, (2011)Human Genome Variation: Disease, Drug Response, and Clinical Phenotypes - Session Introduction., , , and . Pacific Symposium on Biocomputing, page 3-5. (2002)Joint Variant and De Novo Mutation Identification on Pedigrees from High-Throughput Sequencing Data., , , , , , , , , and 3 other author(s). Journal of Computational Biology, 21 (6): 405-419 (2014)