An open resource for accurately benchmarking small variant and reference calls von Zook, Justin M., McDaniel, Jennifer, Olson, Nathan D., Wagner, Justin, Parikh, Hemang, Heaton, Haynes, Irvine, Sean A., Trigg, Len, Truty, Rebecca, McLean, Cory Y., De La Vega, Francisco M., Xiao, Chunlin, Sherry, Stephen, Salit, Marc

Volltext

Escrutinio para el cáncer de colon: ¿cuál fue el impacto en los primeros 2 años de la pandemia de COVID-19? Experiencia en una clínica privada ambulatoria von Teramoto-Matsubara, Óscar, Sobrino-Cossío, Sergio, Abdo-Francis, Juan M., De la Vega-González, Francisco J., Mateos-Pérez, Gualberto

Volltext

Molecular profiling of a real-world breast cancer cohort with genetically inferred ancestries reveals actionable tumor biology differences between European ancestry and African anc... von Miyashita, Minoru, Bell, Joshua S K, Wenric, Stephane, Karaesmen, Ezgi, Rhead, Brooke, Kase, Matthew, Kaneva, Kristiyana, De La Vega, Francisco M, Zheng, Yonglan, Yoshimatsu, Toshio F, Khramtsova, Galina, Liu, Fang, Zhao, Fangyuan, Howard, Frederick M, Nanda, Rita, Beaubier, Nike, White, Kevin P, Huo, Dezheng, Olopade, Olufunmilayo I

Volltext

Best practices for benchmarking germline small-variant calls in human genomes von Krusche, Peter, Trigg, Len, Boutros, Paul C., Mason, Christopher E., De La Vega, Francisco M., Moore, Benjamin L., Gonzalez-Porta, Mar, Eberle, Michael A., Tezak, Zivana, Lababidi, Samir, Truty, Rebecca, Asimenos, George, Funke, Birgit, Fleharty, Mark, Chapman, Brad A., Salit, Marc, Zook, Justin M.

Volltext

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

Volltext

Virtual meetings promise to eliminate geographical and administrative barriers and increase accessibility, diversity and inclusivity von Wu, Juncheng, Rajesh, Anushka, Huang, Yu-Ning, Chhugani, Karishma, Acharya, Rajesh, Peng, Kerui, Johnson, Ruth D, Fiscutean, Andrada, Robles-Espinoza, Carla Daniela, De La Vega, Francisco M, Bao, Riyue, Mangul, Serghei

Volltext

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

Volltext

Distrofia de Fuchs: imágenes con un dispositivo móvil von Francisco Beltrán-Díaz de la Vega, Schenny Murra-Antón

Volltext

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

Volltext

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

Volltext

Integrated genomic characterization of ERBB2/HER2 alterations in invasive breast carcinoma: a focus on unusual FISH groups von Yang, Soo-Ryum, Bouhlal, Yosr, De La Vega, Francisco M., Ballard, Morgan, Kuo, Calvin J., Vilborg, Anna, Jensen, Greg, Allison, Kimberly

Volltext

A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1 von Hampe, Jochen, Schreiber, Stefan, Franke, Andre, Rosenstiel, Philip, Till, Andreas, Teuber, Markus, Huse, Klaus, Albrecht, Mario, Mayr, Gabriele, De La Vega, Francisco M, Briggs, Jason, Günther, Simone, Prescott, Natalie J, Onnie, Clive M, Häsler, Robert, Sipos, Bence, Fölsch, Ulrich R, Lengauer, Thomas, Platzer, Matthias, Mathew, Christopher G, Krawczak, Michael

Volltext

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.

Volltext

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

Volltext

Calidad sensorial de la carne de cabritos lechales criados en sistemas de producción basados en pastoreo von De-la-Vega Galán, Francisco, Guzmán Guerrero, José Luis, Delgado Pertíñez, Manuel, Zarazaga Garcés, Luis Angel, Ruiz Pérez-Cacho, Pilar, Galán-Soldevilla, Hortensia

Volltext

Association of genetic ancestry with molecular tumor profiles in colorectal cancer von Rhead, Brooke, Hein, David M, Pouliot, Yannick, Guinney, Justin, De La Vega, Francisco M, Sanford, Nina N

Volltext

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

Volltext

Inteligencia artificial en la colonoscopia de tamizaje y la disminución del error von Galvis-García, Elymir, De la Vega-González, Francisco J., Emura, Fabian, Teramoto-Matsubara, Óscar, Sánchez-Robles, Juan C., Rodríguez-Vanegas, Gonzalo, Sobrino-Cossío, Sergio

Volltext

Genomics for the world von Bustamante, Carlos D., De La Vega, Francisco M., Burchard, Esteban G.

Volltext

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

Volltext