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ORCIDFrancisco M. de la Vega
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2010 – 2019
- 2015
[c12]Søren Brunak, Francisco M. de la Vega, Adam A. Margolin, Benjamin J. Raphael, Gunnar Rätsch, Joshua M. Stuart:
Session Introduction. Pacific Symposium on Biocomputing 2015: 8-9- 2014
- [j2]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, Francisco M. de la Vega:
Joint Variant and De Novo Mutation Identification on Pedigrees from High-Throughput Sequencing Data. J. Comput. Biol. 21(6): 405-419 (2014) - [c11]Søren Brunak, Francisco M. de la Vega, Gunnar Rätsch, Joshua M. Stuart:
Session Introduction. Pacific Symposium on Biocomputing 2014: 1-2 - 2011
- [c10]Francisco M. de la Vega, Carlos Bustamante, Suzanne M. Leal:
Session Introduction. Pacific Symposium on Biocomputing 2011: 74-75
2000 – 2009
- 2009
- [j1]Michael Brudno, Paul Medvedev, Jens Stoye
, Francisco M. de la Vega:
A report on the 2009 SIG on short read sequencing and algorithms (Short-SIG). Bioinform. 25(21): 2863-2864 (2009) - 2008
- [c9]Francisco M. de la Vega, Gabor T. Marth, Granger G. Sutton:
Session Introduction. Pacific Symposium on Biocomputing 2008: 87-89 - 2006
- [c8]Francisco M. de la Vega, Andrew G. Clark, Andrew Collins, Kenneth K. Kidd:
Session Introduction. Pacific Symposium on Biocomputing 2006: 451-453 - [c7]Francisco M. de la Vega, Hadar I. Isaac, Charles R. Scafe:
A Tool for Selecting SNPs for Association Studies Based on Observed Linkage Disequilibrium Patterns. Pacific Symposium on Biocomputing 2006: 487-498 - 2004
- [c6]Francisco M. de la Vega, Kenneth K. Kidd, Andrew Collins:
Session Introduction. Pacific Symposium on Biocomputing 2004: 89-92 - 2003
- [c5]Francisco M. de la Vega, Kenneth K. Kidd, Isaac S. Kohane:
Human Genome Variation: Haplotypes, Linkage Disequilibrium, and Populations - Session Introduction. Pacific Symposium on Biocomputing 2003: 463-465 - [c4]Hadar I. Avi-Itzhak, Xiaoping Su, Francisco M. de la Vega:
Selection of Minimum Subsets of Single Nucleotide Polymorphisms to Capture Haplotype Block Diversity. Pacific Symposium on Biocomputing 2003: 466-477 - [c3]Josep M. Comeron, Martin Kreitman, Francisco M. de la Vega:
On the Power to Detect SNP/Phenotype Association in Candidate Quantitative Trait Loci Genomic Regions: A Simulation Study. Pacific Symposium on Biocomputing 2003: 478-489 - 2002
- [c2]Francisco M. de la Vega, Isaac S. Kohane, Julie A. Schneider, J. Claiborne Stephens:
Human Genome Variation: Disease, Drug Response, and Clinical Phenotypes - Session Introduction. Pacific Symposium on Biocomputing 2002: 3-5 - 2001
- [c1]Francisco M. de la Vega, Martin Kreitman, Isaac S. Kohane:
Human Genome Variation: Linking Genotypes to Clinical Phenotypes - Session Introduction. Pacific Symposium on Biocomputing 2001: 3-5
Coauthor Index
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