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Featured researches published by Gregg A. Helt.


Science | 2007

RNA Maps Reveal New RNA Classes and a Possible Function for Pervasive Transcription

Philipp Kapranov; Jill Cheng; Sujit Dike; David A. Nix; Radharani Duttagupta; Aarron T. Willingham; Peter F. Stadler; Jana Hertel; Jörg Hackermüller; Ivo L. Hofacker; Ian Bell; Evelyn Cheung; Jorg Drenkow; Erica Dumais; Sandeep Patel; Gregg A. Helt; Madhavan Ganesh; Srinka Ghosh; Antonio Piccolboni; Victor Sementchenko; Hari Tammana; Thomas R. Gingeras

Significant fractions of eukaryotic genomes give rise to RNA, much of which is unannotated and has reduced protein-coding potential. The genomic origins and the associations of human nuclear and cytosolic polyadenylated RNAs longer than 200 nucleotides (nt) and whole-cell RNAs less than 200 nt were investigated in this genome-wide study. Subcellular addresses for nucleotides present in detected RNAs were assigned, and their potential processing into short RNAs was investigated. Taken together, these observations suggest a novel role for some unannotated RNAs as primary transcripts for the production of short RNAs. Three potentially functional classes of RNAs have been identified, two of which are syntenically conserved and correlate with the expression state of protein-coding genes. These data support a highly interleaved organization of the human transcriptome.


BMC Bioinformatics | 2009

Genoviz Software Development Kit: Java tool kit for building genomics visualization applications.

Gregg A. Helt; John W. Nicol; Ed Erwin; Eric Blossom; Steven G. Blanchard; Stephen A. Chervitz; Cyrus L. Harmon; Ann E. Loraine

BackgroundVisualization software can expose previously undiscovered patterns in genomic data and advance biological science.ResultsThe Genoviz Software Development Kit (SDK) is an open source, Java-based framework designed for rapid assembly of visualization software applications for genomics. The Genoviz SDK framework provides a mechanism for incorporating adaptive, dynamic zooming into applications, a desirable feature of genome viewers. Visualization capabilities of the Genoviz SDK include automated layout of features along genetic or genomic axes; support for user interactions with graphical elements (Glyphs) in a map; a variety of Glyph sub-classes that promote experimentation with new ways of representing data in graphical formats; and support for adaptive, semantic zooming, whereby objects change their appearance depending on zoom level and zooming rate adapts to the current scale. Freely available demonstration and production quality applications, including the Integrated Genome Browser, illustrate Genoviz SDK capabilities.ConclusionSeparation between graphics components and genomic data models makes it easy for developers to add visualization capability to pre-existing applications or build new applications using third-party data models. Source code, documentation, sample applications, and tutorials are available at http://genoviz.sourceforge.net/.


Journal of Bioinformatics and Computational Biology | 2003

EXPLORING ALTERNATIVE TRANSCRIPT STRUCTURE IN THE HUMAN GENOME USING BLOCKS AND INTERPRO

Ann E. Loraine; Gregg A. Helt; Melissa S. Cline; Michael A. Siani-Rose

Understanding how alternative splicing affects gene function is an important challenge facing modern-day molecular biology. Using homology-based, protein sequence analysis methods, it should be possible to investigate how transcript diversity impacts protein function. To test this, high-quality exon-intron structures were deduced for over 8000 human genes, including over 1300 (17 percent) that produce multiple transcript variants. A data mining technique (DiffMotif) was developed to identify genes in which transcript variation coincides with changes in conserved motifs between variants. Applying this method, we found that 30 percent of the multi-variant genes in our test set exhibited a differential profile of conserved InterPro and/or BLOCKS motifs across different mRNA variants. To investigate these, a visualization tool (ProtAnnot) that displays amino acid motifs in the context of genomic sequence was developed. Using this tool, genes revealed by the DiffMotif method were analyzed, and when possible, hypotheses regarding the potential role of alternative transcript structure in modulating gene function were developed. Examples of these, including: MEOX1, a homeobox-containing protein; AIRE, involved in auto-immune disease; PLAT, tissue type plasminogen activator; and CD79b, a component of the B-cell receptor complex, are presented. These results demonstrate that amino acid motif databases like BLOCKS and InterPro are useful tools for investigating how alternative transcript structure affects gene function.


Science | 2005

Transcriptional maps of 10 human chromosomes at 5-nucleotide resolution

Jill Cheng; Philipp Kapranov; Jorg Drenkow; Sujit Dike; Shane Brubaker; Sandeep Patel; Jeffrey Long; David Stern; Hari Tammana; Gregg A. Helt; Victor Sementchenko; Antonio Piccolboni; Stefan Bekiranov; Dione K. Bailey; Madhavan Ganesh; Srinka Ghosh; Ian Bell; Daniela S. Gerhard; Thomas R. Gingeras


Cell | 2004

Unbiased Mapping of Transcription Factor Binding Sites along Human Chromosomes 21 and 22 Points to Widespread Regulation of Noncoding RNAs

Simon Cawley; Stefan Bekiranov; Huck H Ng; Philipp Kapranov; Edward A. Sekinger; Dione Kampa; Antonio Piccolboni; Victor Sementchenko; Jill Cheng; Alan Williams; Raymond Wheeler; Brant Wong; Jorg Drenkow; Mark Yamanaka; Sandeep Patel; Shane Brubaker; Hari Tammana; Gregg A. Helt; Kevin Struhl; Thomas R. Gingeras


Genome Research | 2004

Novel RNAs Identified From an In-Depth Analysis of the Transcriptome of Human Chromosomes 21 and 22

Dione Kampa; Jill Cheng; Philipp Kapranov; Mark Yamanaka; Shane Brubaker; Simon Cawley; Jorg Drenkow; Antonio Piccolboni; Stefan Bekiranov; Gregg A. Helt; Hari Tammana; Thomas R. Gingeras


Genome Research | 2005

Examples of the complex architecture of the human transcriptome revealed by RACE and high-density tiling arrays

Philipp Kapranov; Jorg Drenkow; Jill Cheng; Jeffrey C. Long; Gregg A. Helt; Sujit Dike; Thomas R. Gingeras


Archive | 2004

System, method, and computer program product for dynamic display, and analysis of biological sequence data

Gregg A. Helt


BMC Bioinformatics | 2002

Visualizing the genome: techniques for presenting human genome data and annotations

Ann E. Loraine; Gregg A. Helt


Archive | 2003

Method, system and computer software providing a genomic web portal for functional analysis of alternative splice variants

Ann E. Loraine; Melissa S. Cline; Gregg A. Helt; Michael A. Siani-Rose; David Kulp; Ron Shigeta

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Ann E. Loraine

University of North Carolina at Charlotte

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Jorg Drenkow

Cold Spring Harbor Laboratory

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Thomas R. Gingeras

Cold Spring Harbor Laboratory

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