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Bulletin of the World Health Organization|August 4, 2020
Variant analysis of SARS-CoV-2 genomesTakahiko Koyama, Daniel Platt, Laxmi ParidaBioinformatics (Oxford, England)|June 17, 2016
Novel applications of multitask learning and multiple output regression to multiple genetic trait predictionDan He, David Kuhn, Laxmi ParidaTrends in Cancer|July 26, 2017
Watson for Genomics: Moving Personalized Medicine ForwardKahn Rhrissorrakrai, Takahiko Koyama, Laxmi ParidaBMC Cancer|February 3, 2019
Analysis on GENIE reveals novel recurrent variants that affect molecular diagnosis of sizable number of cancer patientsTakahiko Koyama, Kahn Rhrissorrakrai, Laxmi ParidaBMC Bioinformatics|February 25, 2015
Data-driven encoding for quantitative genetic trait predictionDan He, Zhanyong Wang, Laxmi ParidaBMC Genomics|February 2, 2013
Sum of parts is greater than the whole: inference of common genetic history of populationsFilippo Utro, Marc Pybus, Laxmi ParidaIEEE/ACM Transactions on Computational Biology and Bioinformatics|September 11, 2015
Fast Entropic Profiler: An Information Theoretic Approach for the Discovery of Patterns in GenomesMatteo Comin, Morris AntonelloJournal of Integrative Bioinformatics|November 16, 2021
Fast alignment of reads to a variation graph with application to SNP detectionMaurilio Monsu, Matteo CominBMC Bioinformatics|September 26, 2014
Assembly-free genome comparison based on next-generation sequencing reads and variable length patternsMatteo Comin, Michele SchimdJournal of Computational Biology : a Journal of Computational Molecular Cell Biology|March 7, 2014
Parallel continuous flow: a parallel suffix tree construction tool for whole genomesMatteo Comin, Montse FarrerasPageof 17