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Institution

Fred Hutchinson Cancer Research Center

NonprofitCape Town, South Africa
About: Fred Hutchinson Cancer Research Center is a nonprofit organization based out in Cape Town, South Africa. It is known for research contribution in the topics: Population & Transplantation. The organization has 12322 authors who have published 30954 publications receiving 2288772 citations. The organization is also known as: Fred Hutch & The Hutch.


Papers
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Journal ArticleDOI
John Douglas Mcpherson1, Marco A. Marra2, Marco A. Marra1, LaDeana W. Hillier1, Robert H. Waterston1, Asif T. Chinwalla1, John W. Wallis1, Mandeep Sekhon1, Kristine M. Wylie1, Elaine R. Mardis1, Richard K. Wilson1, Robert S. Fulton1, Tamara A. Kucaba1, Caryn Wagner-McPherson1, William B. Barbazuk1, Simon G. Gregory3, Sean Humphray3, Lisa French3, R Evans3, Graeme Bethel3, Adam Whittaker3, Jane L. Holden3, Owen T. McCann3, Andrew Dunham3, Carol Soderlund4, Carol Scott3, David R. Bentley3, Gregory D. Schuler5, Hsiu Chuan Chen5, Wonhee Jang5, Eric D. Green5, Jacquelyn R. Idol5, Valerie Maduro5, Kate Montgomery6, Eunice Lee6, Ashley Miller6, Suzanne Emerling6, Raju Kucherlapati6, Richard A. Gibbs7, Steve Scherer7, J. Harley Gorrell7, Erica Sodergren7, Kerstin P. Clerc-Blankenburg7, Paul E. Tabor7, S. Naylor8, Dawn Garcia8, J. de Jong9, J. de Jong10, J. de Jong11, Joseph J. Catanese9, Joseph J. Catanese11, Joseph J. Catanese10, Norma J. Nowak11, Kazutoyo Osoegawa11, Kazutoyo Osoegawa9, Kazutoyo Osoegawa10, Shizhen Qin12, Lee Rowen12, Anuradha Madan12, Monica Dors12, Leroy Hood12, Barbara J. Trask13, Cynthia Friedman13, Hillary Massa13, Vivian G. Cheung14, Ilan R. Kirsch5, Thomas Reid5, Raluca Yonescu5, Jean Weissenbach, Thomas Brüls, Roland Heilig, Elbert Branscomb15, Anne S. Olsen15, Norman A. Doggett15, Jan Fang Cheng15, Trevor Hawkins15, Richard M. Myers16, Jin Shang16, Lucía Ramírez16, Jeremy Schmutz16, Olivia Velasquez16, Kami Dixon16, Nancy E. Stone16, David R. Cox16, David Haussler17, W. James Kent17, Terrence S. Furey17, Sanja Rogic17, Scot Kennedy17, Steven J.M. Jones2, André Rosenthal5, Gaiping Wen5, Markus Schilhabel5, Gernot Gloeckner5, Gerald Nyakatura5, Reiner Siebert18, Brigitte Schlegelberger18, Julie R. Korenberg19, Xiao Ning Chen19, Asao Fujiyama, Masahira Hattori, Atsushi Toyoda, Tetsushi Yada, Hong Seok Park, Yoshiyuki Sakaki, Nobuyoshi Shimizu20, Shuichi Asakawa20, Kazuhiko Kawasaki20, Takashi Sasaki20, Ai Shintani20, Atsushi Shimizu20, Kazunori Shibuya20, Jun Kudoh20, Shinsei Minoshima20, Juliane Ramser21, Peter Seranski21, Céline Hoff21, Annemarie Poustka21, Richard Reinhardt21, Hans Lehrach21 
15 Feb 2001-Nature
TL;DR: The construction of the whole-genome bacterial artificial chromosome (BAC) map and its integration with previous landmark maps and information from mapping efforts focused on specific chromosomal regions are reported.
Abstract: The human genome is by far the largest genome to be sequenced, and its size and complexity present many challenges for sequence assembly. The International Human Genome Sequencing Consortium constructed a map of the whole genome to enable the selection of clones for sequencing and for the accurate assembly of the genome sequence. Here we report the construction of the whole-genome bacterial artificial chromosome (BAC) map and its integration with previous landmark maps and information from mapping efforts focused on specific chromosomal regions. We also describe the integration of sequence data with the map.

876 citations

Journal ArticleDOI
TL;DR: Emergent trends and gaps in understanding are identified, new approaches to more fully integrate genomics into speciation research are proposed, and an integrative definition of the field of speciation genomics is provided.
Abstract: Speciation is a fundamental evolutionary process, the knowledge of which is crucial for understanding the origins of biodiversity. Genomic approaches are an increasingly important aspect of this research field. We review current understanding of genome-wide effects of accumulating reproductive isolation and of genomic properties that influence the process of speciation. Building on this work, we identify emergent trends and gaps in our understanding, propose new approaches to more fully integrate genomics into speciation research, translate speciation theory into hypotheses that are testable using genomic tools and provide an integrative definition of the field of speciation genomics.

875 citations

Journal ArticleDOI
TL;DR: This paper describes the mathematical models and physical concepts that underlie the latest Rosetta energy function, called the Rosetta Energy Function 2015 (REF15), and explains how to use Rosetta energies to identify and analyze the features of biomolecular models.
Abstract: Over the past decade, the Rosetta biomolecular modeling suite has informed diverse biological questions and engineering challenges ranging from interpretation of low-resolution structural data to design of nanomaterials, protein therapeutics, and vaccines. Central to Rosetta’s success is the energy function: a model parametrized from small-molecule and X-ray crystal structure data used to approximate the energy associated with each biomolecule conformation. This paper describes the mathematical models and physical concepts that underlie the latest Rosetta energy function, called the Rosetta Energy Function 2015 (REF15). Applying these concepts, we explain how to use Rosetta energies to identify and analyze the features of biomolecular models. Finally, we discuss the latest advances in the energy function that extend its capabilities from soluble proteins to also include membrane proteins, peptides containing noncanonical amino acids, small molecules, carbohydrates, nucleic acids, and other macromolecules.

874 citations

Journal ArticleDOI
TL;DR: A group of experts in nutrition, physical activity, and cancer met to evaluate the scientific evidence and best clinical practices related to optimal nutrition and physical activity after the diagnosis of cancer to present health care providers with the best possible information.
Abstract: Cancer survivors are often highly motivated to seek information about food choices, physical activity, dietary supplement use, and complementary nutritional therapies to improve their treatment outcomes, quality of life, and survival. To address these concerns, the American Cancer Society (ACS) convened a group of experts in nutrition, physical activity, and cancer to evaluate the scientific evidence and best clinical practices related to optimal nutrition and physical activity after the diagnosis of cancer. This report summarizes their findings and is intended to present health care providers with the best possible information on which to help cancer survivors and their families make informed choices related to nutrition and physical activity. The report discusses nutrition and physical activity issues during the phases of cancer treatment and recovery, living after recovery from treatment, and living with advanced cancer; selected nutritional and physical activity issues such as body weight, food choices, and complementary and alternative nutritional options; and selected issues related to breast, colorectal, lung, prostate, head and neck, and upper gastrointestinal cancers. In addition, handouts containing commonly asked questions and answers and a resource list are provided for survivors and families. Tables that grade the scientific evidence for benefit versus harm related to nutrition and physical activity for breast, colorectal, lung, and prostate cancers are also included for this growing body of knowledge to provide guidance for informed decision making and to identify areas for future research.

874 citations

Journal ArticleDOI
TL;DR: Nested reverse transcription-PCR analysis revealed cyclin D2 expression in a high proportion of long-term self-renewing HSC, and calculated that approximately 8% of LT-HSC asynchronously entered the cell cycle per day.
Abstract: A rare set of hematopoietic stem cells (HSC) must undergo a massive expansion to produce mature blood cells. The phenotypic isolation of HSC from mice offers the opportunity to determine directly their proliferation kinetics. We analyzed the proliferation and cell cycle kinetics of long-term self-renewing HSC (LT-HSC) in normal adult mice. At any one time, ≈5% of LT-HSC were in S/G2/M phases of the cell cycle and another 20% were in G1 phase. BrdUrd incorporation was used to determine the rate at which different cohorts of HSC entered the cell cycle over time. About 50% of LT-HSC incorporated BrdUrd by 6 days and >90% incorporated BrdUrd by 30 days. By 6 months, 99% of LT-HSC had incorporated BrdUrd. We calculated that approximately 8% of LT-HSC asynchronously entered the cell cycle per day. Nested reverse transcription–PCR analysis revealed cyclin D2 expression in a high proportion of LT-HSC. Although ≈75% of LT-HSC are quiescent in G0 at any one time, all HSC are recruited into cycle regularly such that 99% of LT-HSC divide on average every 57 days.

874 citations


Authors

Showing all 12368 results

NameH-indexPapersCitations
Walter C. Willett3342399413322
Robert Langer2812324326306
Meir J. Stampfer2771414283776
JoAnn E. Manson2701819258509
David J. Hunter2131836207050
Peer Bork206697245427
Eric Boerwinkle1831321170971
Ruedi Aebersold182879141881
Bruce M. Psaty1811205138244
Aaron R. Folsom1811118134044
David Baker1731226109377
Frederick W. Alt17157795573
Lily Yeh Jan16246773655
Yuh Nung Jan16246074818
Charles N. Serhan15872884810
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20237
202275
20211,981
20201,995
20191,685
20181,571