C
Callum J. Bell
Researcher at National Center for Genome Resources
Publications - 48
Citations - 7502
Callum J. Bell is an academic researcher from National Center for Genome Resources. The author has contributed to research in topics: Genome & Gene mapping. The author has an hindex of 29, co-authored 47 publications receiving 6926 citations. Previous affiliations of Callum J. Bell include National Institute for Basic Biology, Japan & University of Pennsylvania.
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Journal ArticleDOI
Assignment of 30 Microsatellite Loci to the Linkage Map of Arabidopsis
Callum J. Bell,Joseph R. Ecker +1 more
TL;DR: After the presence of microsatellites in Arabidopsis and their utility for genetic mapping had been demonstrated, systematic screening for (CA)n and (GA)n sequences was carried out on marker-selected plasmid libraries and a small-insert genomic library.
Journal ArticleDOI
Requirement of the Auxin Polar Transport System in Early Stages of Arabidopsis Floral Bud Formation.
TL;DR: It is suggested that the normal level of polar transport activity in the inflorescence axes is required in early developmental stages of floral bud formation in Arabidopsis and that the primary function of the pin1 gene is auxin polar transport in the inforescence axis.
Journal ArticleDOI
The Marine Microbial Eukaryote Transcriptome Sequencing Project (MMETSP): Illuminating the Functional Diversity of Eukaryotic Life in the Oceans through Transcriptome Sequencing
Patrick J. Keeling,Patrick J. Keeling,Fabien Burki,Heather M. Wilcox,Bassem Allam,Eric E. Allen,Linda A. Amaral-Zettler,Linda A. Amaral-Zettler,E. Virginia Armbrust,John M. Archibald,John M. Archibald,Arvind K. Bharti,Callum J. Bell,Bank Beszteri,Kay D. Bidle,Connor Cameron,Lisa Campbell,David A. Caron,Rose Ann Cattolico,Jackie L. Collier,Kathryn J. Coyne,Simon K. Davy,Phillipe Deschamps,Sonya T. Dyhrman,Bente Edvardsen,Ruth D. Gates,Christopher J. Gobler,Spencer J. Greenwood,Stephanie Guida,Jennifer L. Jacobi,Kjetill S. Jakobsen,Erick R. James,Bethany D. Jenkins,Uwe John,Matthew D. Johnson,Andrew R. Juhl,Anja Kamp,Anja Kamp,Laura A. Katz,Ronald P. Kiene,Alexander Kudryavtsev,Alexander Kudryavtsev,Brian S. Leander,Senjie Lin,Connie Lovejoy,Denis H. Lynn,Denis H. Lynn,Adrian Marchetti,George B. McManus,Aurora M. Nedelcu,Susanne Menden-Deuer,Cristina Miceli,Thomas Mock,Marina Montresor,Mary Ann Moran,Shauna A. Murray,Govind Nadathur,Satoshi Nagai,Peter B. Ngam,Brian Palenik,Jan Pawlowski,Giulio Petroni,Gwenael Piganeau,Matthew C. Posewitz,Karin Rengefors,Giovanna Romano,Mary E. Rumpho,Tatiana A. Rynearson,Kelly B. Schilling,Declan C. Schroeder,Alastair G. B. Simpson,Alastair G. B. Simpson,Claudio H. Slamovits,Claudio H. Slamovits,David Roy Smith,G. Jason Smith,Sarah R. Smith,Heidi M. Sosik,Peter Stief,Edward C. Theriot,Scott N. Twary,Pooja E. Umale,Daniel Vaulot,Boris Wawrik,Glen L. Wheeler,William H. Wilson,Yan Xu,Adriana Zingone,Alexandra Z. Worden,Alexandra Z. Worden +89 more
TL;DR: In this paper, the authors describe a resource of 700 transcriptomes from marine microbial eukaryotes to help understand their role in the world's oceans and their biology, evolution, and ecology.
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Carrier Testing for Severe Childhood Recessive Diseases by Next-Generation Sequencing
Callum J. Bell,Darrell L. Dinwiddie,Darrell L. Dinwiddie,Neil A. Miller,Neil A. Miller,Shannon Hateley,Elena E. Ganusova,Joann Mudge,Raymond J. Langley,Lu Zhang,Clarence Lee,Faye D. Schilkey,Vrunda Sheth,Jimmy E. Woodward,Heather E. Peckham,Gary P. Schroth,Ryan W. Kim,Stephen F. Kingsmore,Stephen F. Kingsmore +18 more
TL;DR: This study provides a proof of concept that it should be possible to introduce preconception carrier screening for many recessive pediatric disease mutations as long as the disease genes are known and predicts that the screening test could be made faster and more cost-effective with the advent of microdroplet polymerase chain reaction and third-generation sequencing technologies.
Journal ArticleDOI
Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis.
Sergio E. Baranzini,Joann Mudge,Jennifer C. van Velkinburgh,Pouya Khankhanian,Irina Khrebtukova,Neil A. Miller,Lu Zhang,Andrew Farmer,Callum J. Bell,Ryan W. Kim,Gregory D. May,Jimmy E. Woodward,Stacy J. Caillier,Joseph P. McElroy,Refujia Gomez,Marcelo J. Pando,Leonda E. Clendenen,Elena E. Ganusova,Faye D. Schilkey,Thiruvarangan Ramaraj,Omar Khan,James Huntley,Shujun Luo,Pui-Yan Kwok,Thomas D. Wu,Gary P. Schroth,Jorge R. Oksenberg,Stephen L. Hauser,Stephen F. Kingsmore +28 more
TL;DR: This first systematic effort to estimate sequence variation among monozygotic co-twins did not find evidence for genetic, epigenetic or transcriptome differences that explained disease discordance, and are the first, to the authors' knowledge, female, twin and autoimmune disease individual genome sequences reported.