Ngā hua rapu - Maika Malig
- E whakaatu ana i te 1 - 20 hua o te 28
- Haere ki te Whārangi Whai Ake
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A Human Genome Structural Variation Sequencing Resource Reveals Insights into Mutational Mechanisms mā 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
I whakaputaina 2010Artigo -
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Population-Genetic Properties of Differentiated Human Copy-Number Polymorphisms mā 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
I whakaputaina 2011Artigo -
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Sequencing of the human IG light chain loci from a hydatidiform mole BAC library reveals locus-specific signatures of genetic diversity mā 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
I whakaputaina 2014Artigo -
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Personalized copy number and segmental duplication maps using next-generation sequencing mā 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
I whakaputaina 2009Artigo -
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Refinement and Discovery of New Hotspots of Copy-Number Variation Associated with Autism Spectrum Disorder mā 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
I whakaputaina 2013Artigo -
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Estimating the human mutation rate using autozygosity in a founder population mā 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
I whakaputaina 2012Artigo -
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Reconstructing complex regions of genomes using long-read sequencing technology mā 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
I whakaputaina 2014Artigo -
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Resolving the complexity of the human genome using single-molecule sequencing mā 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
I whakaputaina 2014Artigo -
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Complete Haplotype Sequence of the Human Immunoglobulin Heavy-Chain Variable, Diversity, and Joining Genes and Characterization of Allelic and Copy-Number Variation mā 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
I whakaputaina 2013Artigo -
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Evolution and diversity of copy number variation in the great ape lineage mā 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
I whakaputaina 2013Artigo -
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Evolution of Human-Specific Neural SRGAP2 Genes by Incomplete Segmental Duplication mā 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
I whakaputaina 2012Artigo -
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A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk mā 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
I whakaputaina 2010Artigo -
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Characterization of missing human genome sequences and copy-number polymorphic insertions mā 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
I whakaputaina 2010Artigo -
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Long-read sequence assembly of the gorilla genome mā 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
I whakaputaina 2016Artigo -
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Structural diversity and African origin of the 17q21.31 inversion polymorphism mā 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
I whakaputaina 2012Artigo -
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Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability mā 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
I whakaputaina 2014Artigo
Ngā utauta rapu:
Ngā marau whai pānga
Biology
Genetics
Gene
Genome
Evolutionary biology
Computational biology
Human genome
Copy-number variation
DNA sequencing
Gene duplication
Population
Allele
Gene family
Segmental duplication
Sociology
Structural variation
Demography
Haplotype
Genotype
Genotyping
Physics
Sequence (biology)
Gene expression
Reference genome
Single-nucleotide polymorphism
Whole genome sequencing
1000 Genomes Project
Anthropology
Astrophysics
DNA