دورية أكاديمية

The Sequence and Analysis of Duplication Rich Human Chromosome 16

التفاصيل البيبلوغرافية
العنوان: The Sequence and Analysis of Duplication Rich Human Chromosome 16
المؤلفون: Martin, Joel, Han, Cliff, Gordon, Laurie A., Terry, Astrid, Prabhakar, Shyam, She, Xinwei, Xie, Gary, Hellsten, Uffe, Chan, Yee Man, Altherr, Michael, Couronne, Olivier, Aerts, Andrea, Bajorek, Eva, Black, Stacey, Blumer, Heather, Branscomb, Elbert, Brown, Nancy C., Bruno, William J., Buckingham, Judith, Callen, David F., Campbell, Connie S., Campbell, Mary L., Campbell, Evelyn W., Caoile, Chenier, Challacombe, Jean F., Chasteen, Lesile A., Chertkov, Olga, Chi, Han C., Christensen, Mari, Clark, Lynn M., Cohn, Judith D., Denys, Mirian, Detter, John C., Dickson, Mark, Dimitrijevic-Bussod, Mira, Escobar, Julio, Fawcett, Joseph J., Flowers, Dave, Fotopulos, Dea, Glavina, Tijina, Gomez, Maria, Gonzales, Eidelyn, Goodstein, David, Goodwin, Lynne A., Grady, Debroah L., Grigoriev, Igor, Groza, Matthew, Hammon, Nancy, Hawkins, Trevor, Haydu, Lauren, Hildebrand, Carl E., Huang, Wayne, Israni, Sanjay, Jett, Jamie, Jewett, Philip E., Kadner, Kristen, Kimball, Heather, Kobayashi, Arthur, Krawczyk, Marie-Claude, Leyba, Tina, Longmire, Jonathan L., Lopez, Frederick, Lou, Yunian, Lowry, Steve, Ludeman, Thom, Manohar, Chitra F., Mark, Graham A., McMurray, Kimberly L., Meincke, Linda J., Morgan, Jenna, Moyzis, Robert K., Mundt, Mark O., Munk, A. Christine, Nandkeshwar, Richard D., Pitluck, Sam, Pollard, Martin, Predki, Paul, Parson-Quintana, Beverly, Ramirez, Lucia, Rash, Sam, Retterer, James, Ricke, Darryl O., Robinson, Donna, Rodriguez, Alex, Salamov, Asaf, Saunders, Elizabeth H., Scott, Duncan, Shough, Timothy, Stallings, Raymond L., Stalvey, Malinda, Sutherland, Robert D., Tapia, Roxanne, Tesmer, Judith G., Thayer, Nina, Thompson, Linda S., Tice, Hope, Torney, David C., Tran-Gyamfi, Mary, Tsai, Ming, Ulanovsky, Levy E., Ustaszewska, Anna, Vo, Nu, White, P. Scott, Williams, Albert L., Wills, Patricia L., Wu, Jung-Rung, Wu, Kevin, Yang, Joan, DeJong, Pieter, Bruce, David, Doggett, Norman A., Deaven, Larry, Schmutz, Jeremy, Grimwood, Jane, Richardson, Paul, Rokhsar, Daniel S., Eichler, Evan E., Gilna, Paul, Lucas, Susan M., Myers, Richard M., Rubin, Edward M., Pennacchio, Len A.
المساهمون: United States. Department of Energy.
المصدر: Journal Name: Nature; Journal Volume: 432
بيانات النشر: Lawrence Livermore National Laboratory
سنة النشر: 2005
المجموعة: University of North Texas: UNT Digital Library
مصطلحات موضوعية: Chromosomes, Diseases, Genes, Leukemia, 59 Basic Biological Sciences, Rna, Metallothionein, Human Chromosome 16, Kidneys, Primates
الوصف: Human chromosome 16 features one of the highest levels of segmentally duplicated sequence among the human autosomes. We report here the 78,884,754 base pairs of finished chromosome 16 sequence, representing over 99.9% of its euchromatin. Manual annotation revealed 880 protein-coding genes confirmed by 1,637 aligned transcripts, 19 tRNA genes, 341 pseudogenes, and 3 RNA pseudogenes. These genes include metallothionein, cadherin, and iroquois gene families, as well as the disease genes for polycystic kidney disease and acute myelomonocytic leukemia. Several large-scale structural polymorphisms spanning hundreds of kilobase pairs were identified and result in gene content differences among humans. While the segmental duplications of chromosome 16 are enriched in the relatively gene poor pericentromere of the p-arm, some are involved in recent gene duplication and conversion events likely to have had an impact on the evolution of primates and human disease susceptibility.
نوع الوثيقة: article in journal/newspaper
وصف الملف: PDF-file: 31 pages; size: 0.5 Mbytes; Text
اللغة: English
العلاقة: rep-no: UCRL-JRNL-211171; grantno: W-7405-ENG-48; osti: 875361; https://digital.library.unt.edu/ark:/67531/metadc878367Test/; ark: ark:/67531/metadc878367
الإتاحة: https://digital.library.unt.edu/ark:/67531/metadc878367Test/
رقم الانضمام: edsbas.BD7F26BE
قاعدة البيانات: BASE