检索结果 - Heather E. Peckham

  • Showing 1 - 12 results of 12
Refine Results
  1. 1
    Nucleosome positioning signals in genomic DNA

    Nucleosome positioning signals in genomic DNA 由 Heather E. Peckham, Robert E. Thurman, Yutao Fu, J Stamatoyannopoulos, William Stafford Noble, Kevin Struhl, Zhiping Weng

    出版 2007
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  2. 2
    Whole Methylome Analysis by Ultra-Deep Sequencing Using Two-Base Encoding

    Whole Methylome Analysis by Ultra-Deep Sequencing Using Two-Base Encoding 由 Christina A. Bormann Chung, Victoria L. Boyd, Kevin McKernan, Yutao Fu, Cinna K. Monighetti, Heather E. Peckham, Melissa Barker

    出版 2010
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  3. 3
    A high-resolution, nucleosome position map of <i>C. elegans</i> reveals a lack of universal sequence-dictated positioning

    A high-resolution, nucleosome position map of <i>C. elegans</i> reveals a lack of universal sequence-dictated positioning 由 Anton Valouev, Jeffrey K. Ichikawa, Thaisan Tonthat, Jeremy Stuart, Swati Ranade, Heather E. Peckham, Kathy Zeng, Joel A. Malek, Gina L. Costa, Kevin McKernan, Arend Sidow, Andrew Fire, Steven Johnson

    出版 2008
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  4. 4
    A comprehensively molecular haplotype-resolved genome of a European individual

    A comprehensively molecular haplotype-resolved genome of a European individual 由 Eun-Kyung Suk, Gayle K. McEwen, Jorge Duitama, Katja Nowick, Sabrina Schulz, Stefanie Palczewski, Stefan Schreiber, Dustin Holloway, Stephen McLaughlin, Heather E. Peckham, Clarence Lee, Thomas Huebsch, Margret R. Hoehe

    出版 2011
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  5. 5
    Chromatin and sequence features that define the fine and gross structure of genomic methylation patterns

    Chromatin and sequence features that define the fine and gross structure of genomic methylation patterns 由 John R. Edwards, Anne O’Donnell‐Luria, Robert A. Rollins, Heather E. Peckham, Clarence Lee, Maria H. Milekic, Benjamin Chanrion, Yutao Fu, Tao Su, Hanina Hibshoosh, Jay A. Gingrich, Fatemeh Haghighi, Robert C. Nutter, Timothy H. Bestor

    出版 2010
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  6. 6
    A Novel Fusion of TPR and ALK in Lung Adenocarcinoma

    A Novel Fusion of TPR and ALK in Lung Adenocarcinoma 由 Yoon‐La Choi, Maruja E. Lira, Min Eui Hong, Ryong Nam Kim, So‐Jung Choi, Ji‐Young Song, Kinnari Pandy, Derrick L. Mann, Joshua A. Stahl, Heather E. Peckham, Zongli Zheng, Joungho Han, Mao Mao, Young Tae Kim

    出版 2014
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  7. 7
    Carrier Testing for Severe Childhood Recessive Diseases by Next-Generation Sequencing

    Carrier Testing for Severe Childhood Recessive Diseases by Next-Generation Sequencing 由 Callum J. Bell, Darrell L. Dinwiddie, Neil Miller, Shannon Hateley, Elena E. Ganusova, Joann Mudge, Ray J. Langley, Lu Zhang, Clarence Lee, Faye Schilkey, Vrunda Sheth, Jimmy E. Woodward, Heather E. Peckham, Gary P. Schroth, Ryan W. Kim, Stephen F. Kingsmore

    出版 2011
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  8. 8
    Rapid whole-genome mutational profiling using next-generation sequencing technologies

    Rapid whole-genome mutational profiling using next-generation sequencing technologies 由 Andrew R. Smith, Aaron R. Quinlan, Heather E. Peckham, Kathryn Makowsky, Wei Tao, Betty Woolf, Lei Shen, William F. Donahue, Nadeem Tusneem, Michael P. Strömberg, Donald A. Stewart, Lu Zhang, Swati Ranade, Jason Warner, Clarence Lee, B E Coleman, Zheng Zhang, Stephen F. McLaughlin, Joel A. Malek, Jon M. Sorenson, Alan P. Blanchard, Jarrod Chapman, David R. Hillman, Feng Chen, Daniel S. Rokhsar, Kevin McKernan, Thomas W. Jeffries, Gábor Marth, Paul M. Richardson

    出版 2008
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  9. 9
    Population Genetic Inference from Personal Genome Data: Impact of Ancestry and Admixture on Human Genomic Variation

    Population Genetic Inference from Personal Genome Data: Impact of Ancestry and Admixture on Human Genomic Variation 由 Jeffrey M. Kidd, Simon Gravel, Jake Byrnes, Andrés Moreno‐Estrada, Shaila Musharoff, Katarzyna Bryc, Jeremiah D. Degenhardt, Abra Brisbin, Vrunda Sheth, Rong Chen, Stephen F. McLaughlin, Heather E. Peckham, Larsson Omberg, Christina A. Bormann Chung, Sarah A. Stanley, Kevin A. Pearlstein, Elizabeth Levandowsky, Suehelay Acevedo‐Acevedo, Adam Auton, Alon Keinan, Víctor Acuña-Alonzo, Rodrigo Barquera, Samuel Canizales‐Quinteros, Celeste Eng, Esteban G. Burchard, Archie Russell, Andy Reynolds, Andrew G. Clark, Martin G. Reese, Stephen E. Lincoln, Atul J. Butte, Francisco M. De La Vega, Carlos D. Bustamante

    出版 2012
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  10. 10
    A small-cell lung cancer genome with complex signatures of tobacco exposure

    A small-cell lung cancer genome with complex signatures of tobacco exposure 由 Erin Pleasance, Philip J. Stephens, Sarah O’Meara, David J. McBride, Alison Meynert, David Jones, Meng‐Lay Lin, David Beare, King Wai Lau, Chris Greenman, Ignacio Varela, Serena Nik‐Zainal, Helen Davies, Gonzalo R. Ordóñez, Laura Mudie, Calli Latimer, Sarah Edkins, Lucy Stebbings, Lina Chen, Mingming Jia, Catherine Leroy, John Marshall, Andrew Menzies, Adam P. Butler, Jon W. Teague, Jonathon Mangion, Yongming Sun, Stephen F. McLaughlin, Heather E. Peckham, Eric F. Tsung, Gina L. Costa, Clarence Lee, John D. Minna, Adi F. Gazdar, Ewan Birney, Michael D. Rhodes, Kevin McKernan, Michael R. Stratton, P. Andrew Futreal, Peter J. Campbell

    出版 2009
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  11. 11
    Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding

    Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding 由 Kevin McKernan, Heather E. Peckham, Gina L. Costa, Stephen F. McLaughlin, Yutao Fu, Eric F. Tsung, Christopher R. Clouser, Cisyla Duncan, Jeffrey K. Ichikawa, Clarence Lee, Zheng Zhang, Swati Ranade, Eileen T. Dimalanta, Fiona Hyland, Tanya Sokolsky, Lei Zhang, Andrew Sheridan, Haoning Fu, Cynthia L. Hendrickson, Bin Li, Lev Kotler, Jeremy R Stuart, Joel A. Malek, Jonathan M. Manning, Alena A Antipova, Damon S. Perez, Michael P. Moore, Kathleen Hayashibara, M.R. Lyons, Robert E. Beaudoin, Brittany E. Coleman, Michael W. Laptewicz, Adam E. Sannicandro, Michael D. Rhodes, Rajesh Gottimukkala, Shan Yang, Vineet Bafna, Ali Bashir, Andrew R. MacBride, Can Alkan, Jeffrey M. Kidd, Evan E. Eichler, Martin G. Reese, Francisco M. De La Vega, Alan P. Blanchard

    出版 2009
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  12. 12
    Mapping copy number variation by population-scale genome sequencing

    Mapping copy number variation by population-scale genome sequencing 由 Ryan E. Mills, Klaudia Walter, Chip Stewart, Robert E. Handsaker, Ken Chen, Can Alkan, Alexej Abyzov, Seungtai Yoon, Kai Ye, R. Keira Cheetham, Asif Chinwalla, Donald F. Conrad, Yutao Fu, Fabian Grubert, Iman Hajirasouliha, Fereydoun Hormozdiari, Lilia M. Iakoucheva, Zamin Iqbal, Shuli Kang, Jeffrey M. Kidd, Miriam K. Konkel, Joshua M. Korn, Ekta Khurana, Deniz Kural, Hugo Y. K. Lam, Jing Leng, Ruiqiang Li, Yingrui Li, Chang‐Yun Lin, Ruibang Luo, Xinmeng Jasmine Mu, James Nemesh, Heather E. Peckham, Tobias Rausch, Aylwyn Scally, Xinghua Shi, Michael P. Strömberg, Adrian M. Stütz, Alexander E. Urban, Jerilyn A. Walker, Jiantao Wu, Goo Jun, Zhengdong D. Zhang, Mark A. Batzer, Li Ding, Gábor Marth, Gil McVean, Jonathan Sebat, M Snyder, Jun Wang, Kenny Ye, Evan E. Eichler, Mark Gerstein, Matthew E. Hurles, Charles Lee, Steven A. McCarroll, Jan O. Korbel

    出版 2011
    获取全文
    Artigo
    加到收藏夹
    Saved in:

检索工具: