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Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|November 30, 2016
DE NOVO MUTATIONS IN AUTISM IMPLICATE THE SYNAPTIC ELIMINATION NETWORKGuhan Ram Venkataraman, Chloe O'Connell, Fumiko Egawa, et al.
Genome Biology|May 7, 2015
Fast and scalable inference of multi-sample cancer lineagesVictoria Popic, Raheleh Salari, Iman Hajirasouliha, et al.
Bioinformatics (Oxford, England)|June 21, 2011
Reconstruction of genealogical relationships with applications to Phase III of HapMapSofia Kyriazopoulou-Panagiotopoulou, Dorna Kashef Haghighi, Sarah J Aerni, et al.
Genome Research|August 20, 2015
Read clouds uncover variation in complex regions of the human genomeAlex Bishara, Yuling Liu, Ziming Weng, et al.
Journal of Computational Biology : a Journal of Computational Molecular Cell Biology|November 8, 2013
Inference of tumor phylogenies with improved somatic mutation discoveryRaheleh Salari, Syed Shayon Saleh, Dorna Kashef-Haghighi, et al.
Genome Medicine|April 29, 2015
Cell-lineage heterogeneity and driver mutation recurrence in pre-invasive breast neoplasiaZiming Weng, Noah Spies, Shirley X Zhu, et al.
Genome Research|April 10, 2013
Genome evolution during progression to breast cancerDaniel E Newburger, Dorna Kashef-Haghighi, Ziming Weng, et al.
Cell|August 10, 2019
Inherited and De Novo Genetic Risk for Autism Impacts Shared NetworksElizabeth K Ruzzo, Laura Pérez-Cano, Jae-Yoon Jung, et al.
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