المؤلفون: Nuttle, Xander, Giannuzzi, Giuliana, Duyzend, Michael H, Schraiber, Joshua G, Narvaiza, Iñigo, Sudmant, Peter H, Penn, Osnat, Chiatante, Giorgia, Malig, Maika, Huddleston, John, Benner, Chris, Camponeschi, Francesca, Ciofi-Baffoni, Simone, Stessman, Holly AF, Marchetto, Maria CN, Denman, Laura, Harshman, Lana, Baker, Carl, Raja, Archana, Penewit, Kelsi, Janke, Nicolette, Tang, W Joyce, Ventura, Mario, Banci, Lucia, Antonacci, Francesca, Akey, Joshua M, Amemiya, Chris T, Gage, Fred H, Reymond, Alexandre, Eichler, Evan E

المصدر: Nature. 536(7615)

مصطلحات موضوعية: Chromosomes, Human, Pair 16, Animals, Humans, Pan troglodytes, Chromosome Breakage, Genetic Predisposition to Disease, Iron, Proteins, Autistic Disorder, Evolution, Molecular, Species Specificity, Gene Duplication, Recombination, Genetic, Homeostasis, Time Factors, DNA Copy Number Variations, Pongo, Human Genome, Genetics, Biotechnology, General Science & Technology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/84x6d03kTest

المؤلفون: Chaisson, Mark JP, Huddleston, John, Dennis, Megan Y, Sudmant, Peter H, Malig, Maika, Hormozdiari, Fereydoun, Antonacci, Francesca, Surti, Urvashi, Sandstrom, Richard, Boitano, Matthew, Landolin, Jane M, Stamatoyannopoulos, John A, Hunkapiller, Michael W, Korlach, Jonas, Eichler, Evan E

المصدر: Nature. 517(7536)

مصطلحات موضوعية: Genetics, Human Genome, Generic health relevance, Chromosome Inversion, Chromosomes, Human, Pair 10, Cloning, Molecular, GC Rich Sequence, Genetic Variation, Genome, Human, Genomics, Haploidy, Humans, Mutagenesis, Insertional, Reference Standards, Sequence Analysis, DNA, Tandem Repeat Sequences, General Science & Technology

الوصول الحر: https://escholarship.org/uc/item/78k994t1Test

المؤلفون: Antonacci, Francesca, Dennis, Megan Y, Huddleston, John, Sudmant, Peter H, Steinberg, Karyn Meltz, Rosenfeld, Jill A, Miroballo, Mattia, Graves, Tina A, Vives, Laura, Malig, Maika, Denman, Laura, Raja, Archana, Stuart, Andrew, Tang, Joyce, Munson, Brenton, Shaffer, Lisa G, Amemiya, Chris T, Wilson, Richard K, Eichler, Evan E

المصدر: Nature genetics. 46(12)

مصطلحات موضوعية: Chromosomes, Artificial, Bacterial, Chromosomes, Human, Pair 15, Animals, Primates, Humans, Seizures, Chromosome Disorders, Chromosome Deletion, In Situ Hybridization, Fluorescence, Cluster Analysis, Sequence Analysis, DNA, Repetitive Sequences, Nucleic Acid, Gene Dosage, Polymorphism, Genetic, Genome, Human, Models, Genetic, Comparative Genomic Hybridization, Segmental Duplications, Genomic, Biological Evolution, Intellectual Disability, Genetics, Biological Sciences, Medical and Health Sciences, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/2nk6g212Test

المؤلفون: Huddleston, John, Ranade, Swati, Malig, Maika, Antonacci, Francesca, Chaisson, Mark, Hon, Lawrence, Sudmant, Peter H, Graves, Tina A, Alkan, Can, Dennis, Megan Y, Wilson, Richard K, Turner, Stephen W, Korlach, Jonas, Eichler, Evan E

المصدر: Genome Research. 24(4)

مصطلحات موضوعية: Biotechnology, Human Genome, Genetics, Generic health relevance, Animals, Chromosomes, Artificial, Bacterial, Chromosomes, Human, Pair 17, Genome, Bacterial, High-Throughput Nucleotide Sequencing, Humans, Mice, Molecular Sequence Data, Pan troglodytes, Biological Sciences, Medical and Health Sciences, Bioinformatics

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/50x6m7m0Test

المؤلفون: Steinberg, Karyn Meltz, Antonacci, Francesca, Sudmant, Peter H, Kidd, Jeffrey M, Campbell, Catarina D, Vives, Laura, Malig, Maika, Scheinfeldt, Laura, Beggs, William, Ibrahim, Muntaser, Lema, Godfrey, Nyambo, Thomas B, Omar, Sabah A, Bodo, Jean-Marie, Froment, Alain, Donnelly, Michael P, Kidd, Kenneth K, Tishkoff, Sarah A, Eichler, Evan E

المصدر: Nature Genetics. 44(8)

مصطلحات موضوعية: Genetics, Africa, Black People, Chromosome Inversion, Chromosomes, Human, Pair 17, Evolution, Molecular, Gene Frequency, Haplotypes, Humans, In Situ Hybridization, Fluorescence, Linkage Disequilibrium, Phylogeny, Polymorphism, Genetic, Polymorphism, Single Nucleotide, Biological Sciences, Medical and Health Sciences, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/5f02g432Test

المؤلفون: Chaisson M. J. P., Huddleston J., Dennis M. Y., Sudmant P. H., Malig M., Hormozdiari F., Antonacci F., Surti U., Sandstrom R., Boitano M., Landolin J. M., Stamatoyannopoulos J. A., Hunkapiller M. W., Korlach J., Eichler E. E.

المساهمون: Chaisson, M. J. P., Huddleston, J., Dennis, M. Y., Sudmant, P. H., Malig, M., Hormozdiari, F., Antonacci, F., Surti, U., Sandstrom, R., Boitano, M., Landolin, J. M., Stamatoyannopoulos, J. A., Hunkapiller, M. W., Korlach, J., Eichler, E. E.

مصطلحات موضوعية: Chromosome Inversion, Chromosomes, Human, Pair 10, Cloning, Molecular, GC Rich Sequence, Genetic Variation, Genome, Haploidy, Mutagenesis, Insertional, Reference Standard, Sequence Analysis, DNA, Tandem Repeat Sequence, Genomics

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/25383537; info:eu-repo/semantics/altIdentifier/wos/WOS:000348775000042; volume:517; issue:7536; firstpage:608; lastpage:611; numberofpages:4; journal:NATURE; http://hdl.handle.net/11586/359839Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84925497196

الإتاحة: https://doi.org/10.1038/nature13907Test
http://hdl.handle.net/11586/359839Test