Torthaí cuardaigh - Can Alkan

Beachtaigh na torthaí
  1. 1
    Limitations of next-generation genome sequence assembly

    Limitations of next-generation genome sequence assembly de réir Can Alkan, Saba Sajjadian, Evan E. Eichler

    Foilsithe / Cruthaithe 2010
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  2. 2
    Genome structural variation discovery and genotyping

    Genome structural variation discovery and genotyping de réir Can Alkan, Bradley P. Coe, Evan E. Eichler

    Foilsithe / Cruthaithe 2011
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  3. 3
    Combinatorial algorithms for structural variation detection in high-throughput sequenced genomes

    Combinatorial algorithms for structural variation detection in high-throughput sequenced genomes de réir Fereydoun Hormozdiari, Can Alkan, Evan E. Eichler, S. Cenk Şahinalp

    Foilsithe / Cruthaithe 2009
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  4. 4
    Shouji: a fast and efficient pre-alignment filter for sequence alignment

    Shouji: a fast and efficient pre-alignment filter for sequence alignment de réir Mohammed Alser, Hasan Hassan, Akash Kumar, Onur Mutlu, Can Alkan

    Foilsithe / Cruthaithe 2019
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  5. 5
    Nanopore sequencing technology and tools for genome assembly: computational analysis of the current state, bottlenecks and future directions

    Nanopore sequencing technology and tools for genome assembly: computational analysis of the current state, bottlenecks and future directions de réir Damla Senol Cali, Jeremie S. Kim, Saugata Ghose, Can Alkan, Onur Mutlu

    Foilsithe / Cruthaithe 2018
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  6. 6
    Accelerating read mapping with FastHASH

    Accelerating read mapping with FastHASH de réir Hongyi Xin, Donghyuk Lee, Farhad Hormozdiari, Samihan Yedkar, Onur Mutlu, Can Alkan

    Foilsithe / Cruthaithe 2013
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  7. 7
    Comparative analysis of <i>Alu</i> repeats in primate genomes

    Comparative analysis of <i>Alu</i> repeats in primate genomes de réir George E. Liu, Can Alkan, Jiang Lu, Shaying Zhao, Evan E. Eichler

    Foilsithe / Cruthaithe 2009
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  8. 8
    GateKeeper: a new hardware architecture for accelerating pre-alignment in DNA short read mapping

    GateKeeper: a new hardware architecture for accelerating pre-alignment in DNA short read mapping de réir Mohammed Alser, Hasan Hassan, Hongyi Xin, Oğuz Ergin, Onur Mutlu, Can Alkan

    Foilsithe / Cruthaithe 2017
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  9. 9
    mrsFAST-Ultra: a compact, SNP-aware mapper for high performance sequencing applications

    mrsFAST-Ultra: a compact, SNP-aware mapper for high performance sequencing applications de réir Faraz Hach, Iman Sarrafi, Farhad Hormozdiari, Can Alkan, Evan E. Eichler, S. Cenk Şahinalp

    Foilsithe / Cruthaithe 2014
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  10. 10
    Fast characterization of segmental duplications in genome assemblies

    Fast characterization of segmental duplications in genome assemblies de réir Ibrahim Numanagić, Alim Şükrücan Gökkaya, Lillian Zhang, Bonnie Berger, Can Alkan, Faraz Hach

    Foilsithe / Cruthaithe 2018
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  11. 11
    Shifted Hamming distance: a fast and accurate SIMD-friendly filter to accelerate alignment verification in read mapping

    Shifted Hamming distance: a fast and accurate SIMD-friendly filter to accelerate alignment verification in read mapping de réir Hongyi Xin, John Greth, John Emmons, Gennady Pekhimenko, Carl Kingsford, Can Alkan, Onur Mutlu

    Foilsithe / Cruthaithe 2015
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  12. 12
    mrsFAST: a cache-oblivious algorithm for short-read mapping

    mrsFAST: a cache-oblivious algorithm for short-read mapping de réir Faraz Hach, Fereydoun Hormozdiari, Can Alkan, Farhad Hormozdiari, İnanç Birol, Evan E. Eichler, S. Cenk Şahinalp

    Foilsithe / Cruthaithe 2010
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  13. 13
    Accelerating Genome Analysis: A Primer on an Ongoing Journey

    Accelerating Genome Analysis: A Primer on an Ongoing Journey de réir Mohammed Alser, Zülal Bingöl, Damla Senol Cali, Jeremie Kim, Saugata Ghose, Can Alkan, Onur Mutlu

    Foilsithe / Cruthaithe 2020
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  14. 14
    Detection and characterization of novel sequence insertions using paired-end next-generation sequencing

    Detection and characterization of novel sequence insertions using paired-end next-generation sequencing de réir Iman Hajirasouliha, Fereydoun Hormozdiari, Can Alkan, Jeffrey M. Kidd, İnanç Birol, Evan E. Eichler, S. Cenk Şahinalp

    Foilsithe / Cruthaithe 2010
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  15. 15
    Apollo: a sequencing-technology-independent, scalable and accurate assembly polishing algorithm

    Apollo: a sequencing-technology-independent, scalable and accurate assembly polishing algorithm de réir Can Fırtına, Jeremie S. Kim, Mohammed Alser, Damla Senol Cali, A. Ercüment Çiçek, Can Alkan, Onur Mutlu

    Foilsithe / Cruthaithe 2020
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  16. 16
    Early postzygotic mutations contribute to de novo variation in a healthy monozygotic twin pair

    Early postzygotic mutations contribute to de novo variation in a healthy monozygotic twin pair de réir Gülşah M Dal, Bekir Ergüner, Mahmut Şamil Sağıroğlu, Bayram Yüksel, Onur Emre Onat, Can Alkan, Tayfun Özçelık

    Foilsithe / Cruthaithe 2014
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  17. 17
    Next-generation VariationHunter: combinatorial algorithms for transposon insertion discovery

    Next-generation VariationHunter: combinatorial algorithms for transposon insertion discovery de réir Fereydoun Hormozdiari, Iman Hajirasouliha, Phuong Dao, Faraz Hach, Deniz Yörükoğlu, Can Alkan, Evan E. Eichler, S. Cenk Şahinalp

    Foilsithe / Cruthaithe 2010
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  18. 18
    GRIM-Filter: Fast seed location filtering in DNA read mapping using processing-in-memory technologies

    GRIM-Filter: Fast seed location filtering in DNA read mapping using processing-in-memory technologies de réir Jeremie S. Kim, Damla Senol Cali, Hongyi Xin, Donghyuk Lee, Saugata Ghose, Mohammed Alser, Hasan Hassan, Oğuz Ergin, Can Alkan, Onur Mutlu

    Foilsithe / Cruthaithe 2018
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  19. 19
    Analysis of Primate Genomic Variation Reveals a Repeat-Driven Expansion of the Human Genome

    Analysis of Primate Genomic Variation Reveals a Repeat-Driven Expansion of the Human Genome de réir Ge Liu, NISC Comparative Sequencing Program, Shaying Zhao, Jeffrey A. Bailey, S. Cenk Şahinalp, Can Alkan, Eray Tüzün, Eric D. Green, Evan E. Eichler

    Foilsithe / Cruthaithe 2003
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  20. 20
    Diversity of Human Copy Number Variation and Multicopy Genes

    Diversity of Human Copy Number Variation and Multicopy Genes de réir Peter H. Sudmant, Jacob O. Kitzman, Francesca Antonacci, Can Alkan, Maika Malig, Anya Tsalenko, Nick Sampas, Laurakay Bruhn, Jay Shendure, Evan E. Eichler

    Foilsithe / Cruthaithe 2010
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