Suchergebnisse - De La Vega, Francisco M

Polygenic risk scores: a biased prediction? von De La Vega, Francisco M., Bustamante, Carlos D.

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GENOME-WIDE ASSOCIATION MAPPING AND RARE ALLELES: FROM POPULATION GENOMICS TO PERSONALIZED MEDICINE von DE LA VEGA, FRANCISCO M., BUSTAMANTE, CARLOS D., LEAL, SUZANNE M.

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Genomics for the world: Medical genomics has focused almost entirely on those of European descent. Other ethnic groups must be studied to ensure that more people benefit, say von Bustamante, Carlos D., Burchard, Esteban González, De La Vega, Francisco M.

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Inexpensive and Highly Reproducible Cloud-Based Variant Calling of 2,535 Human Genomes von Shringarpure, Suyash S., Carroll, Andrew, De La Vega, Francisco M., Bustamante, Carlos D.

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Evolution of Yeast Noncoding RNAs Reveals an Alternative Mechanism for Widespread Intron Loss von Mitrovich, Quinn M., Tuch, Brian B., De La Vega, Francisco M., Guthrie, Christine, Johnson, Alexander D.

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Global analysis of disease-related DNA sequence variation in 10 healthy individuals: Implications for whole genome-based clinical diagnostics von Moore, Barry, Hu, Hao, Singleton, Marc, De La Vega, Francisco M., Reese, Martin G., Yandell, Mark

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Population genetic analysis of shotgun assemblies of genomic sequences from multiple individuals von Hellmann, Ines, Mang, Yuan, Gu, Zhiping, Li, Peter, de la Vega, Francisco M., Clark, Andrew G., Nielsen, Rasmus

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Optimal Haplotype Block-Free Selection of Tagging SNPs for Genome-Wide Association Studies von Halldórsson, Bjarni V., Bafna, Vineet, Lippert, Ross, Schwartz, Russell, De La Vega, Francisco M., Clark, Andrew G., Istrail, Sorin

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Identifying Selected Regions from Heterozygosity and Divergence Using a Light-Coverage Genomic Dataset from Two Human Populations von Oleksyk, Taras K., Zhao, Kai, De La Vega, Francisco M., Gilbert, Dennis A., O'Brien, Stephen J., Smith, Michael W.

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Analyses of a set of 128 ancestry informative single-nucleotide polymorphisms in a global set of 119 population samples von Kidd, Judith R, Friedlaender, Françoise R, Speed, William C, Pakstis, Andrew J, De La Vega, Francisco M, Kidd, Kenneth K

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The Transcriptomes of Two Heritable Cell Types Illuminate the Circuit Governing Their Differentiation von Tuch, Brian B., Mitrovich, Quinn M., Homann, Oliver R., Hernday, Aaron D., Monighetti, Cinna K., De La Vega, Francisco M., Johnson, Alexander D.

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Clinical Pertinence Metric Enables Hypothesis-Independent Genome-Phenome Analysis for Neurologic Diagnosis von Segal, Michael M., Abdellateef, Mostafa, El-Hattab, Ayman W., Hilbush, Brian S., De La Vega, Francisco M., Tromp, Gerard, Williams, Marc S., Betensky, Rebecca A., Gleeson, Joseph

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Nucleosome regulatory dynamics in response to TGFβ von Enroth, Stefan, Andersson, Robin, Bysani, Madhusudhan, Wallerman, Ola, Termén, Stefan, Tuch, Brian B., De La Vega, Francisco M., Heldin, Carl-Henrik, Moustakas, Aristidis, Komorowski, Jan, Wadelius, Claes

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Genome sequencing and analysis of admixed genomes of African and Mexican ancestry: implications for personal ancestry reconstruction and multi-ethnic medical genomics von De La Vega, Francisco M, Bryc, Katarzyna, Degehnardt, Jeremiah D, Musharoff, Shaila, Kidd, Jeffrey M, Seth, Vrunda, Stanley, Sarah, Brisbin, Abra, Keinan, Alon, Clark, Andrew, Bustamante, Carlos D

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Racial and Ethnic Differences in Genomic Profiling of Early Onset Colorectal Cancer von Hein, David M, Deng, Weiye, Bleile, MaryLena, Kazmi, Syed Ali, Rhead, Brooke, De La Vega, Francisco M, Jones, Amy L, Kainthla, Radhika, Jiang, Wen, Cantarel, Brandi, Sanford, Nina N

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Using genotype array data to compare multi- and single-sample variant calls and improve variant call sets from deep coverage whole-genome sequencing data von Shringarpure, Suyash S, Mathias, Rasika A, Hernandez, Ryan D, O’Connor, Timothy D, Szpiech, Zachary A, Torres, Raul, De La Vega, Francisco M, Bustamante, Carlos D, Barnes, Kathleen C, Taub, Margaret A

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A robust targeted sequencing approach for low input and variable quality DNA from clinical samples von So, Austin P., Vilborg, Anna, Bouhlal, Yosr, Koehler, Ryan T., Grimes, Susan M., Pouliot, Yannick, Mendoza, Daniel, Ziegle, Janet, Stein, Jason, Goodsaid, Federico, Lucero, Michael Y., De La Vega, Francisco M., Ji, Hanlee P.

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An ancestry informative marker set for determining continental origin: validation and extension using human genome diversity panels von Nassir, Rami, Kosoy, Roman, Tian, Chao, White, Phoebe A, Butler, Lesley M, Silva, Gabriel, Kittles, Rick, Alarcon-Riquelme, Marta E, Gregersen, Peter K, Belmont, John W, De La Vega, Francisco M, Seldin, Michael F

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Ancestry Informative Marker Sets for Determining Continental Origin and Admixture Proportions in Common Populations in America von Kosoy, Roman, Nassir, Rami, Tian, Chao, White, Phoebe A, Butler, Lesley M., Silva, Gabriel, Kittles, Rick, Alarcon-Riquelme, Marta E., Gregersen, Peter K., Belmont, John W., De La Vega, Francisco M., Seldin, Michael F.

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A second-generation combined linkage–physical map of the human genome von Matise, Tara C., Chen, Fang, Chen, Wenwei, De La Vega, Francisco M., Hansen, Mark, He, Chunsheng, Hyland, Fiona C.L., Kennedy, Giulia C., Kong, Xiangyang, Murray, Sarah S., Ziegle, Janet S., Stewart, William C.L., Buyske, Steven

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