Francisco M. de la Vega

According to our database, Francisco M. de la Vega authored at least 15 papers between 2001 and 2026.

Collaborative distances:

• Dijkstra number of four.
• Erdős number of four.

2026

Efficient Chromosome Parallelization for Precision Medicine Genomic Workflows.

Daniel Mas Montserrat, Ray Verma, Míriam Barrabés, Francisco M. de la Vega, Carlos D. Bustamante, Alexander G. Ioannidis

Proceedings of the Fortieth AAAI Conference on Artificial Intelligence, 2026

2015

Session Introduction.

Søren Brunak, Francisco M. de la Vega, Adam A. Margolin, Benjamin J. Raphael, Gunnar Rätsch, Joshua M. Stuart

Proceedings of the Biocomputing 2015: Proceedings of the Pacific Symposium, 2015

2014

Joint Variant and <i>De Novo</i> 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, Francisco M. de la Vega

J. Comput. Biol., 2014

Session Introduction.

Søren Brunak, Francisco M. de la Vega, Gunnar Rätsch, Joshua M. Stuart

Proceedings of the Biocomputing 2014: Proceedings of the Pacific Symposium, 2014

2011

Session Introduction.

Francisco M. de la Vega, Carlos Bustamante, Suzanne M. Leal

Proceedings of the Biocomputing 2011: Proceedings of the Pacific Symposium, 2011

2009

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

2008

Session Introduction.

Francisco M. de la Vega, Gabor T. Marth, Granger G. Sutton

Proceedings of the Biocomputing 2008, 2008

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

Proceedings of the Biocomputing 2006, 2006

Session Introduction.

Francisco M. de la Vega, Andrew G. Clark, Andrew Collins, Kenneth K. Kidd

Proceedings of the Biocomputing 2006, 2006

2004

Session Introduction.

Francisco M. de la Vega, Kenneth K. Kidd, Andrew Collins

Proceedings of the Biocomputing 2004, 2004

2003

Human Genome Variation: Haplotypes, Linkage Disequilibrium, and Populations - Session Introduction.

Francisco M. de la Vega, Kenneth K. Kidd, Isaac S. Kohane

Proceedings of the 8th 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

Proceedings of the 8th Pacific Symposium on Biocomputing, 2003

Selection of Minimum Subsets of Single Nucleotide Polymorphisms to Capture Haplotype Block Diversity.

Hadar I. Avi-Itzhak, Xiaoping Su, Francisco M. de la Vega

Proceedings of the 8th Pacific Symposium on Biocomputing, 2003

2002

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

Proceedings of the 7th Pacific Symposium on Biocomputing, 2002

2001

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

Francisco M. de la Vega, Martin Kreitman, Isaac S. Kohane

Proceedings of the 6th Pacific Symposium on Biocomputing, 2001