Human Genome Variation: Linking Genotypes to Clinical Phenotypes - Session Introduction. - Francisco M. de la Vega; Martin Kreitman; Isaac S. Kohane (Pacific Symposium on Biocomputing, 2001)

Human Genome Variation: Disease, Drug Response, and Clinical Phenotypes - Session Introduction. - Francisco M. de la Vega; Isaac S. Kohane; Julie A. Schneider; J. Claiborne Stephens (Pacific Symposium on Biocomputing, 2002)

Selection of Minimum Subsets of Single Nucleotide Polymorphisms to Capture Haplotype Block Diversity. - Hadar I. Avi-Itzhak; Xiaoping Su; Francisco M. de la Vega (Pacific Symposium on Biocomputing, 2003)

On the Power to Detect SNP/Phenotype Association in Candidate Quantitative Trait Loci Genomic Regions: A Simulation Study. - Josep M. Comeron; Martin Kreitman; Francisco M. de la Vega (Pacific Symposium on Biocomputing, 2003)

Human Genome Variation: Haplotypes, Linkage Disequilibrium, and Populations - Session Introduction. - Francisco M. de la Vega; Kenneth K. Kidd; Isaac S. Kohane (Pacific Symposium on Biocomputing, 2003)

Session Introduction. - Francisco M. de la Vega; Kenneth K. Kidd; Andrew Collins 001 (Pacific Symposium on Biocomputing, 2004)

Session Introduction. - Francisco M. de la Vega; Andrew G. Clark; Andrew Collins 001; Kenneth K. Kidd (Pacific Symposium on Biocomputing, 2006)

A Tool for Selecting SNPs for Association Studies Based on Observed Linkage Disequilibrium Patterns. - Francisco M. de la Vega; Hadar I. Isaac; Charles R. Scafe (Pacific Symposium on Biocomputing, 2006)

Session Introduction. - Francisco M. de la Vega; Gabor T. Marth; Granger G. Sutton (Pacific Symposium on Biocomputing, 2008)

A report on the 2009 SIG on short read sequencing and algorithms (Short-SIG). - Michael Brudno; Paul Medvedev; Jens Stoye; Francisco M. de la Vega (Bioinform., 2009)

Session Introduction. - Francisco M. de la Vega; Carlos Bustamante; Suzanne M. Leal (Pacific Symposium on Biocomputing, 2011)

Session Introduction. - Søren Brunak; Francisco M. de la Vega; Gunnar Rätsch; Joshua M. Stuart (Pacific Symposium on Biocomputing, 2014)

Joint Variant and De Novo Mutation Identification on Pedigrees from High-Throughput Sequencing Data. - John G. Cleary; Ross Braithwaite; Kurt Gaastra; Brian S. Hilbush; Stuart Inglis; Sean A. Irvine; Alan Jackson; Richard Littin; Sahar Nohzadeh-Malakshah; Mehul Rathod; David Ware; Len Trigg; et al. (J. Comput. Biol., 2014)

Session Introduction. - Søren Brunak; Francisco M. de la Vega; Adam A. Margolin; Benjamin J. Raphael; Gunnar Rätsch; Joshua M. Stuart (Pacific Symposium on Biocomputing, 2015)