Searching journal content for S W Scherer in author.

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  1. Research: Resolving complex duplication variants in autism spectrum disorder using long-read genome sequencing
    • Jesper Eisfeldt,
    • Edward J. Higginbotham,
    • Felix Lenner,
    • Jennifer Howe,
    • Bridget A. Fernandez,
    • Anna Lindstrand,
    • Stephen W. Scherer,
    • and Lars Feuk
    Genome Res. November 2024 34: 1763-1773; Published in Advance October 29, 2024, doi:10.1101/gr.279263.124
    OPEN ACCESS ARTICLE
  2. Method: An efficient genotyper and star-allele caller for pharmacogenomics
    • Ananth Hari,
    • Qinghui Zhou,
    • Nina Gonzaludo,
    • John Harting,
    • Stuart A. Scott,
    • Xiang Qin,
    • Steve Scherer,
    • S. Cenk Sahinalp,
    • and Ibrahim Numanagić
    Genome Res. January 2023 33: 61-70; Published in Advance January 19, 2023, doi:10.1101/gr.277075.122
  3. Research: Postmortem genetic screening for the identification, verification, and reporting of genetic variants contributing to the sudden death of the young
    • D. Nicole R. Methner,
    • Steven E. Scherer,
    • Katherine Welch,
    • Magdalena Walkiewicz,
    • Christine M. Eng,
    • John W. Belmont,
    • Mark C. Powell,
    • Viktoriya Korchina,
    • Harsha Vardhan Doddapaneni,
    • Donna M. Muzny,
    • Richard A. Gibbs,
    • Dwayne A. Wolf,
    • Luis A. Sanchez,
    • and Roger Kahn
    Genome Res. September 2016 26: 1170-1177; Published in Advance July 19, 2016, doi:10.1101/gr.195800.115
  4. Insight/Outlook: The ethics of conducting molecular autopsies in cases of sudden death in the young
    • Amy L. McGuire,
    • Quianta Moore,
    • Mary Majumder,
    • Magdalena Walkiewicz,
    • Christine M. Eng,
    • John W. Belmont,
    • Salma Nassef,
    • Sandra Darilek,
    • Katie Rutherford,
    • Stacey Pereira,
    • Steven E. Scherer,
    • V. Reid Sutton,
    • Dwayne Wolf,
    • Richard A. Gibbs,
    • Roger Kahn,
    • Luis A. Sanchez,
    • and the Molecular Autopsy Consortium of Houston (MATCH)
    Genome Res. September 2016 26: 1165-1169; Published in Advance July 13, 2016, doi:10.1101/gr.192401.115
  5. Resource: Comparative validation of the D. melanogaster modENCODE transcriptome annotation
    • Zhen-Xia Chen,
    • David Sturgill,
    • Jiaxin Qu,
    • Huaiyang Jiang,
    • Soo Park,
    • Nathan Boley,
    • Ana Maria Suzuki,
    • Anthony R. Fletcher,
    • David C. Plachetzki,
    • Peter C. FitzGerald,
    • Carlo G. Artieri,
    • Joel Atallah,
    • Olga Barmina,
    • James B. Brown,
    • Kerstin P. Blankenburg,
    • Emily Clough,
    • Abhijit Dasgupta,
    • Sai Gubbala,
    • Yi Han,
    • Joy C. Jayaseelan,
    • Divya Kalra,
    • Yoo-Ah Kim,
    • Christie L. Kovar,
    • Sandra L. Lee,
    • Mingmei Li,
    • James D. Malley,
    • John H. Malone,
    • Tittu Mathew,
    • Nicolas R. Mattiuzzo,
    • Mala Munidasa,
    • Donna M. Muzny,
    • Fiona Ongeri,
    • Lora Perales,
    • Teresa M. Przytycka,
    • Ling-Ling Pu,
    • Garrett Robinson,
    • Rebecca L. Thornton,
    • Nehad Saada,
    • Steven E. Scherer,
    • Harold E. Smith,
    • Charles Vinson,
    • Crystal B. Warner,
    • Kim C. Worley,
    • Yuan-Qing Wu,
    • Xiaoyan Zou,
    • Peter Cherbas,
    • Manolis Kellis,
    • Michael B. Eisen,
    • Fabio Piano,
    • Karin Kionte,
    • David H. Fitch,
    • Paul W. Sternberg,
    • Asher D. Cutter,
    • Michael O. Duff,
    • Roger A. Hoskins,
    • Brenton R. Graveley,
    • Richard A. Gibbs,
    • Peter J. Bickel,
    • Artyom Kopp,
    • Piero Carninci,
    • Susan E. Celniker,
    • Brian Oliver,
    • and Stephen Richards
    Genome Res. July 2014 24: 1209-1223; Published in Advance July 1, 2014, doi:10.1101/gr.159384.113
    OPEN ACCESS ARTICLE
  6. Method: Sequencing of isolated sperm cells for direct haplotyping of a human genome
    • Ewen F. Kirkness,
    • Rashel V. Grindberg,
    • Joyclyn Yee-Greenbaum,
    • Christian R. Marshall,
    • Stephen W. Scherer,
    • Roger S. Lasken,
    • and J. Craig Venter
    Genome Res. May 2013 23: 826-832; Published in Advance January 2, 2013, doi:10.1101/gr.144600.112
  7. Research: Whole-exome sequencing combined with functional genomics reveals novel candidate driver cancer genes in endometrial cancer
    • Han Liang,
    • Lydia W.T. Cheung,
    • Jie Li,
    • Zhenlin Ju,
    • Shuangxing Yu,
    • Katherine Stemke-Hale,
    • Turgut Dogruluk,
    • Yiling Lu,
    • Xiuping Liu,
    • Chao Gu,
    • Wei Guo,
    • Steven E. Scherer,
    • Hannah Carter,
    • Shannon N. Westin,
    • Mary D. Dyer,
    • Roeland G.W. Verhaak,
    • Fan Zhang,
    • Rachel Karchin,
    • Chang-Gong Liu,
    • Karen H. Lu,
    • Russell R. Broaddus,
    • Kenneth L. Scott,
    • Bryan T. Hennessy,
    • and Gordon B. Mills
    Genome Res. November 2012 22: 2120-2129; Published in Advance October 1, 2012, doi:10.1101/gr.137596.112
  8. Method: A novel approach identifies new differentially methylated regions (DMRs) associated with imprinted genes
    • Sanaa Choufani,
    • Jonathan S. Shapiro,
    • Martha Susiarjo,
    • Darci T. Butcher,
    • Daria Grafodatskaya,
    • Youliang Lou,
    • Jose C. Ferreira,
    • Dalila Pinto,
    • Stephen W. Scherer,
    • Lisa G. Shaffer,
    • Philippe Coullin,
    • Isabella Caniggia,
    • Joseph Beyene,
    • Rima Slim,
    • Marisa S. Bartolomei,
    • and Rosanna Weksberg
    Genome Res. March 2011 21: 465-476; Published in Advance February 7, 2011, doi:10.1101/gr.111922.110
  9. LETTER: A sequence-level map of chromosomal breakpoints in the MCF-7 breast cancer cell line yields insights into the evolution of a cancer genome
    • Oliver A. Hampton,
    • Petra Den Hollander,
    • Christopher A. Miller,
    • David A. Delgado,
    • Jian Li,
    • Cristian Coarfa,
    • Ronald A. Harris,
    • Stephen Richards,
    • Steven E. Scherer,
    • Donna M. Muzny,
    • Richard A. Gibbs,
    • Adrian V. Lee,
    • and Aleksandar Milosavljevic
    Genome Res. February 2009 19: 167-177; Published in Advance December 3, 2008, doi:10.1101/gr.080259.108
    OPEN ACCESS ARTICLE
  10. LETTER: Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencing
    • David Monk,
    • Alexandre Wagschal,
    • Philippe Arnaud,
    • Pari-Sima Müller,
    • Layla Parker-Katiraee,
    • Déborah Bourc’his,
    • Stephen W. Scherer,
    • Robert Feil,
    • Philip Stanier,
    • and Gudrun E. Moore
    Genome Res. August 2008 18: 1270-1281; Published in Advance May 14, 2008, doi:10.1101/gr.077115.108
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