Resultados de procura - Maika Malig

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  1. 1
    Ultra-deep Coverage Single-molecule R-loop Footprinting Reveals Principles of R-loop Formation

    Ultra-deep Coverage Single-molecule R-loop Footprinting Reveals Principles of R-loop Formation por Maika Malig, Stella R. Hartono, Jenna M. Giafaglione, Lionel A. Sanz, Frédéric Chédin

    Publicado 2020
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  2. 2
    Interplay between DNA sequence and negative superhelicity drives R-loop structures

    Interplay between DNA sequence and negative superhelicity drives R-loop structures por Robert Stolz, Shaheen Sulthana, Stella R. Hartono, Maika Malig, Craig J. Benham, Frédéric Chédin

    Publicado 2019
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  3. 3
    Diversity of Human Copy Number Variation and Multicopy Genes

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

    Publicado 2010
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  4. 4
    A Human Genome Structural Variation Sequencing Resource Reveals Insights into Mutational Mechanisms

    A Human Genome Structural Variation Sequencing Resource Reveals Insights into Mutational Mechanisms por Jeffrey M. Kidd, Tina Graves, Tera L. Newman, Robert S. Fulton, Hillary S. Hayden, Maika Malig, Joelle Kallicki, Rajinder Kaul, Richard K. Wilson, Evan E. Eichler

    Publicado 2010
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  5. 5
    Copy number variation detection and genotyping from exome sequence data

    Copy number variation detection and genotyping from exome sequence data por Niklas Krumm, Peter H. Sudmant, Arthur Ko, Brian J. O’Roak, Maika Malig, Bradley P. Coe, Aaron R. Quinlan, Deborah A. Nickerson, Evan E. Eichler

    Publicado 2012
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  6. 6
    Population-Genetic Properties of Differentiated Human Copy-Number Polymorphisms

    Population-Genetic Properties of Differentiated Human Copy-Number Polymorphisms por Catarina D. Campbell, Nick Sampas, Anya Tsalenko, Peter H. Sudmant, Jeffrey M. Kidd, Maika Malig, Tiffany Vu, Laura Vives, Peter Tsang, Laurakay Bruhn, Evan E. Eichler

    Publicado 2011
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  7. 7
    Sequencing of the human IG light chain loci from a hydatidiform mole BAC library reveals locus-specific signatures of genetic diversity

    Sequencing of the human IG light chain loci from a hydatidiform mole BAC library reveals locus-specific signatures of genetic diversity por Corey T. Watson, Karyn Meltz Steinberg, Tina Graves, Robin M. Warren, Maika Malig, Jacqueline E. Schein, Richard K. Wilson, Robert A. Holt, Evan E. Eichler, Felix Breden

    Publicado 2014
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  8. 8
    Personalized copy number and segmental duplication maps using next-generation sequencing

    Personalized copy number and segmental duplication maps using next-generation sequencing por 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

    Publicado 2009
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  9. 9
    Refinement and Discovery of New Hotspots of Copy-Number Variation Associated with Autism Spectrum Disorder

    Refinement and Discovery of New Hotspots of Copy-Number Variation Associated with Autism Spectrum Disorder por Santhosh Girirajan, Megan Y. Dennis, Carl Baker, Maika Malig, Bradley P. Coe, Colin Campbell, Kenneth M. K. Mark, Tiffany Vu, Can Alkan, Ze Cheng, Leslie G. Biesecker, Raphael Bernier, Evan E. Eichler

    Publicado 2013
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  10. 10
    Estimating the human mutation rate using autozygosity in a founder population

    Estimating the human mutation rate using autozygosity in a founder population por Catarina D. Campbell, Jessica X. Chong, Maika Malig, Arthur Ko, Beth L. Dumont, Lide Han, Laura Vives, Brian J. O’Roak, Peter H. Sudmant, Jay Shendure, Mark Abney, Carole Ober, Evan E. Eichler

    Publicado 2012
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  11. 11
    Reconstructing complex regions of genomes using long-read sequencing technology

    Reconstructing complex regions of genomes using long-read sequencing technology por John Huddleston, Swati Ranade, Maika Malig, Francesca Antonacci, Mark Chaisson, Lawrence Hon, Peter H. Sudmant, Tina Graves, Can Alkan, Megan Y. Dennis, Richard K. Wilson, Stephen W. Turner, Jonas Korlach, Evan E. Eichler

    Publicado 2014
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  12. 12
    Resolving the complexity of the human genome using single-molecule sequencing

    Resolving the complexity of the human genome using single-molecule sequencing por 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

    Publicado 2014
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  13. 13
    Complete Haplotype Sequence of the Human Immunoglobulin Heavy-Chain Variable, Diversity, and Joining Genes and Characterization of Allelic and Copy-Number Variation

    Complete Haplotype Sequence of the Human Immunoglobulin Heavy-Chain Variable, Diversity, and Joining Genes and Characterization of Allelic and Copy-Number Variation por Corey T. Watson, Karyn Meltz Steinberg, John Huddleston, Robin M. Warren, Maika Malig, Jacqueline E. Schein, A. Jeremy Willsey, Jeffrey B. Joy, Jamie K. Scott, Tina Graves, Richard K. Wilson, Robert A. Holt, Evan E. Eichler, Felix Breden

    Publicado 2013
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  14. 14
    Evolution and diversity of copy number variation in the great ape lineage

    Evolution and diversity of copy number variation in the great ape lineage por Peter H. Sudmant, John Huddleston, Claudia Rita Catacchio, Maika Malig, LaDeana W. Hillier, Carl Baker, Kiana Mohajeri, Ivanela Kondova, Ronald E. Bontrop, Stephan P. Persengiev, Francesca Antonacci, Mario Ventura, Javier Prado-Martinez, Tomàs Marquès‐Bonet, Evan E. Eichler

    Publicado 2013
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  15. 15
    Evolution of Human-Specific Neural SRGAP2 Genes by Incomplete Segmental Duplication

    Evolution of Human-Specific Neural SRGAP2 Genes by Incomplete Segmental Duplication por Megan Y. Dennis, Xander Nuttle, Peter H. Sudmant, Francesca Antonacci, Tina Graves, Mikhail Nefedov, Jill A. Rosenfeld, Saba Sajjadian, Maika Malig, Holland Kotkiewicz, Cynthia J. Curry, Susan Shafer, Lisa G. Shaffer, Pieter J. de Jong, Richard K. Wilson, Evan E. Eichler

    Publicado 2012
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  16. 16
    A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk

    A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk por Francesca Antonacci, Jeffrey M. Kidd, Tomàs Marquès‐Bonet, Brian Teague, Mario Ventura, Santhosh Girirajan, Can Alkan, Colin Campbell, Laura Vives, Maika Malig, Jill A. Rosenfeld, Blake C. Ballif, Lisa G. Shaffer, Tina Graves, Richard K. Wilson, David C. Schwartz, Evan E. Eichler

    Publicado 2010
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  17. 17
    Characterization of missing human genome sequences and copy-number polymorphic insertions

    Characterization of missing human genome sequences and copy-number polymorphic insertions por Jeffrey M. Kidd, Nick Sampas, Francesca Antonacci, Tina Graves, Robert S. Fulton, Hillary S. Hayden, Can Alkan, Maika Malig, Mario Ventura, Giuliana Giannuzzi, Joelle Kallicki, Paige Anderson, Anya Tsalenko, N. Alice Yamada, Peter Tsang, Rajinder Kaul, Richard K. Wilson, Laurakay Bruhn, Evan E. Eichler

    Publicado 2010
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  18. 18
    Long-read sequence assembly of the gorilla genome

    Long-read sequence assembly of the gorilla genome por David Gordon, John Huddleston, Mark Chaisson, C. Hill, Zev Kronenberg, Katherine M. Munson, Maika Malig, Archana N. Raja, Ian T. Fiddes, LaDeana Hillier, Christopher Dunn, Carl Baker, Joel Armstrong, Mark Diekhans, Benedict Paten, Jay Shendure, Richard K. Wilson, David Haussler, Chen-Shan Chin, Evan E. Eichler

    Publicado 2016
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  19. 19
    Structural diversity and African origin of the 17q21.31 inversion polymorphism

    Structural diversity and African origin of the 17q21.31 inversion polymorphism por Karyn Meltz Steinberg, Francesca Antonacci, Peter H. Sudmant, Jeffrey M. Kidd, Colin Campbell, Laura Vives, Maika Malig, Laura Scheinfeldt, William Beggs, Muntaser E. Ibrahim, Godfrey Lema, Thomas Nyambo, Sabah A. Omar, Jean-Marie Bodo, Alain Froment, Michael P. Donnelly, Kenneth K. Kídd, Sarah A. Tishkoff, Evan E. Eichler

    Publicado 2012
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  20. 20
    Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability

    Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability por Francesca Antonacci, Megan Y. Dennis, John Huddleston, Peter H. Sudmant, Karyn Meltz Steinberg, Jill A. Rosenfeld, Mattia Miroballo, Tina Graves, Laura Vives, Maika Malig, Laura Denman, Archana N. Raja, Andrew B. Stuart, Joyce Tang, Brenton P. Munson, Lisa G. Shaffer, Chris T. Amemiya, Richard K. Wilson, Evan E. Eichler

    Publicado 2014
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