Zoekresultaten - Fereydoun Hormozdiari
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The discovery of integrated gene networks for autism and related disorders door Fereydoun Hormozdiari, Osnat Penn, Elhanan Borenstein, Evan E. Eichler
Gepubliceerd in 2014Artigo -
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Biomolecular network motif counting and discovery by color coding door Noga Alon, Phuong Dao, Iman Hajirasouliha, Fereydoun Hormozdiari, S. Cenk Şahinalp
Gepubliceerd in 2008Artigo -
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mrsFAST: a cache-oblivious algorithm for short-read mapping door Faraz Hach, Fereydoun Hormozdiari, Can Alkan, Farhad Hormozdiari, İnanç Birol, Evan E. Eichler, S. Cenk Şahinalp
Gepubliceerd in 2010Carta -
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Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity door Bradley P. Coe, Holly A.F. Stessman, Arvis Sulovari, Madeleine R. Geisheker, Trygve E. Bakken, Allison M. Lake, Joseph D. Dougherty, Ed S. Lein, Fereydoun Hormozdiari, Raphael Bernier, Evan E. Eichler
Gepubliceerd in 2018Artigo -
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Personalized copy number and segmental duplication maps using next-generation sequencing door Can Alkan, Jeffrey M. Kidd, Tomàs Marquès‐Bonet, Gozde Aksay, Francesca Antonacci, Fereydoun Hormozdiari, Jacob O. Kitzman, Carl Baker, Maika Malig, Onur Mutlu, S. Cenk Şahinalp, Richard A. Gibbs, Evan E. Eichler
Gepubliceerd in 2009Artigo -
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Genomic Patterns of De Novo Mutation in Simplex Autism door Tychele N. Turner, Bradley P. Coe, Diane E. Dickel, Kendra Hoekzema, Bradley J. Nelson, Michael C. Zody, Zev Kronenberg, Fereydoun Hormozdiari, Archana N. Raja, L Pennacchio, Robert B. Darnell, Evan E. Eichler
Gepubliceerd in 2017Artigo -
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Resolving the complexity of the human genome using single-molecule sequencing door Mark Chaisson, John Huddleston, Megan Y. Dennis, Peter H. Sudmant, Maika Malig, Fereydoun Hormozdiari, Francesca Antonacci, Urvashi Surti, Richard Sandstrom, Matthew Boitano, Jane M. Landolin, J Stamatoyannopoulos, Michael W. Hunkapiller, Jonas Korlach, Evan E. Eichler
Gepubliceerd in 2014Artigo -
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deFuse: An Algorithm for Gene Fusion Discovery in Tumor RNA-Seq Data door Andrew McPherson, Fereydoun Hormozdiari, Abdalnasser Zayed, Ryan Giuliany, Gavin Ha, Mark Sun, Malachi Griffith, Alireza Heravi Moussavi, Janine Senz, Nataliya Melnyk, Marina Pacheco, Marco A. Marra, Martin Hirst, Torsten O. Nielsen, S. Cenk Şahinalp, David G. Huntsman, Sohrab P. Shah
Gepubliceerd in 2011Artigo -
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Rates and patterns of great ape retrotransposition door Fereydoun Hormozdiari, Miriam K. Konkel, Javier Prado-Martinez, Giorgia Chiatante, Irene Hernando Herraez, Jerilyn A. Walker, B.E. Nelson, Can Alkan, Peter H. Sudmant, John Huddleston, Claudia Rita Catacchio, Arthur Ko, Maika Malig, Carl Baker, Great Ape Genome Project, Tomàs Marquès‐Bonet, Mario Ventura, Mark A. Batzer, Evan E. Eichler
Gepubliceerd in 2013Artigo -
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Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA door Tychele N. Turner, Fereydoun Hormozdiari, Michael H. Duyzend, Sarah A. McClymont, Paul W. Hook, Ivan Iossifov, Archana N. Raja, Carl Baker, Kendra Hoekzema, Holly A.F. Stessman, Michael C. Zody, Bradley J. Nelson, John Huddleston, Richard Sandstrom, Joshua D. Smith, D. Hanna, James M. Swanson, Elaine M. Faustman, Michael J. Bamshad, J Stamatoyannopoulos, Deborah A. Nickerson, Andrew S. McCallion, Robert B. Darnell, Evan E. Eichler
Gepubliceerd in 2015Artigo -
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Deep generative AI models analyzing circulating orphan non-coding RNAs enable detection of early-stage lung cancer door Mehran Karimzadeh, Amir Momen-Roknabadi, Taylor B. Cavazos, Yuqi Fang, Nae-Chyun Chen, Michael Multhaup, Jennifer Yen, Jeremy Ku, Jieyang Wang, Xuan Zhao, Philip Murzynowski, Kathleen Wang, Rose Hanna, Alice Huang, Diana Corti, Dang Le Tri Nguyen, Ti Lam, Seda Kilinc, Patrick Arensdorf, Kimberly H. Chau, Anna Hartwig, Lisa Fish, Helen Li, Babak Behsaz, Olivier Elemento, James Zou, Fereydoun Hormozdiari, Babak Alipanahi, Hani Goodarzi
Gepubliceerd in 2024Artigo -
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From sequence to molecular pathology, and a mechanism driving the neuroendocrine phenotype in prostate cancer door Anna Lapuk, Chunxiao Wu, Alexander W. Wyatt, Andrew McPherson, Brian McConeghy, Sonal Brahmbhatt, Fan Mo, Amina Zoubeidi, Shawn Anderson, Robert H. Bell, Anne Haegert, Robert Shukin, Yuzhuo Wang, Ladan Fazli, Antonio Hurtado‐Coll, Edward C. Jones, Faraz Hach, Fereydoun Hormozdiari, Iman Hajirasouliha, Paul C. Boutros, Robert G. Bristow, Zhao Yong-jun, Marco A. Marra, Andrea Fanjul, Christopher A. Maher, Arul M. Chinnaiyan, Mark A. Rubin, Himisha Beltran, S. Cenk Şahinalp, Martin Gleave, Stanislav Volik, Colin C. Collins
Gepubliceerd in 2012Artigo -
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Integrated genome and transcriptome sequencing identifies a novel form of hybrid and aggressive prostate cancer door Chunxiao Wu, Alexander W. Wyatt, Anna Lapuk, Andrew McPherson, Brian McConeghy, Robert H. Bell, Shawn Anderson, Anne Haegert, Sonal Brahmbhatt, Robert Shukin, Fan Mo, Estelle Li, Ladan Fazli, Antonio Hurtado‐Coll, Edward C. Jones, Yaron S.N. Butterfield, Faraz Hach, Fereydoun Hormozdiari, Iman Hajirasouliha, Paul C. Boutros, Robert G. Bristow, Steven J.M. Jones, Martin Hirst, Marco A. Marra, Christopher A. Maher, Arul M. Chinnaiyan, S. Cenk Şahinalp, Martin Gleave, Stanislav Volik, Colin C. Collins
Gepubliceerd in 2012Artigo -
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The genome sequencing of an albino Western lowland gorilla reveals inbreeding in the wild door Javier Prado-Martinez, Irene Hernando-Herraez, Belén Lorente-Galdós, Marc Dabad, Óscar Ramírez, Carlos Baeza-Delgado, Carlos Morcillo-Suárez, Can Alkan, Fereydoun Hormozdiari, Emanuele Raineri, Jordi Estellé, Marcos Fernández-Callejo, Mònica Vallès, Lars Ritscher, Torsten Schöneberg, Elisa de la Calle‐Mustienes, Sònia Casillas, Raquel Rubio‐Acero, Marta Melé, Johannes Engelken, Mario Cáceres, José Luis Gómez-Skármeta, Marta Gut, Jaume Bertranpetit, Marta Gut, Teresa Abelló, Evan E. Eichler, Ismael Mingarro, Carles Lalueza‐Fox, Arcadi Navarro, Tomàs Marquès‐Bonet
Gepubliceerd in 2013Artigo
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Biology
Genetics
Gene
Genome
Computational biology
Structural variation
Human genome
Computer science
Genotype
Single-nucleotide polymorphism
DNA sequencing
Evolutionary biology
1000 Genomes Project
Copy-number variation
Reference genome
Indel
Medicine
Population
Demography
Haplotype
Mutation
Sociology
Whole genome sequencing
Allele
Gene expression
Transposable element
Autism
Bioinformatics
Exome sequencing
Genomics