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Dive into the research topics where Chandra L. Theesfeld is active.

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Featured researches published by Chandra L. Theesfeld.


Nucleic Acids Research | 2004

The Gene Ontology (GO) database and informatics resource.

Midori A. Harris; Jennifer I. Clark; Amelia Ireland; Jane Lomax; Michael Ashburner; R. Foulger; K. Eilbeck; Suzanna E. Lewis; B. Marshall; Christopher J. Mungall; John Richter; Gerald M. Rubin; Judith A. Blake; Mary E. Dolan; Harold J. Drabkin; Janan T. Eppig; David P. Hill; Li Ni; Martin Ringwald; Rama Balakrishnan; J. M. Cherry; Karen R. Christie; Maria C. Costanzo; Selina S. Dwight; Stacia R. Engel; Dianna G. Fisk; Jodi E. Hirschman; Eurie L. Hong; Robert S. Nash; Anand Sethuraman

The Gene Ontology (GO) project (http://www. geneontology.org/) provides structured, controlled vocabularies and classifications that cover several domains of molecular and cellular biology and are freely available for community use in the annotation of genes, gene products and sequences. Many model organism databases and genome annotation groups use the GO and contribute their annotation sets to the GO resource. The GO database integrates the vocabularies and contributed annotations and provides full access to this information in several formats. Members of the GO Consortium continually work collectively, involving outside experts as needed, to expand and update the GO vocabularies. The GO Web resource also provides access to extensive documentation about the GO project and links to applications that use GO data for functional analyses.


Nucleic Acids Research | 2004

Saccharomyces Genome Database (SGD) provides tools to identify and analyze sequences from Saccharomyces cerevisiae and related sequences from other organisms

Karen R. Christie; Shuai Weng; Rama Balakrishnan; Maria C. Costanzo; Kara Dolinski; Selina S. Dwight; Stacia R. Engel; Becket Feierbach; Dianna G. Fisk; Jodi E. Hirschman; Eurie L. Hong; Laurie Issel-Tarver; Robert S. Nash; Anand Sethuraman; Barry Starr; Chandra L. Theesfeld; Rey Andrada; Gail Binkley; Qing Dong; Christopher Lane; Mark Schroeder; David Botstein; J. Michael Cherry

The Saccharomyces Genome Database (SGD; http://www.yeastgenome.org/), a scientific database of the molecular biology and genetics of the yeast Saccharomyces cerevisiae, has recently developed several new resources that allow the comparison and integration of information on a genome-wide scale, enabling the user not only to find detailed information about individual genes, but also to make connections across groups of genes with common features and across different species. The Fungal Alignment Viewer displays alignments of sequences from multiple fungal genomes, while the Sequence Similarity Query tool displays PSI-BLAST alignments of each S.cerevisiae protein with similar proteins from any species whose sequences are contained in the non-redundant (nr) protein data set at NCBI. The Yeast Biochemical Pathways tool integrates groups of genes by their common roles in metabolism and displays the metabolic pathways in a graphical form. Finally, the Find Chromosomal Features search interface provides a versatile tool for querying multiple types of information in SGD.


Genome Biology | 2005

Discovery of biological networks from diverse functional genomic data

Chad L. Myers; Drew Robson; Adam Wible; Matthew A. Hibbs; Camelia Chiriac; Chandra L. Theesfeld; Kara Dolinski; Olga G. Troyanskaya

We have developed a general probabilistic system for query-based discovery of pathway-specific networks through integration of diverse genome-wide data. This framework was validated by accurately recovering known networks for 31 biological processes in Saccharomyces cerevisiae and experimentally verifying predictions for the process of chromosomal segregation. Our system, bioPIXIE, a public, comprehensive system for integration, analysis, and visualization of biological network predictions for S. cerevisiae, is freely accessible over the worldwide web.


Nucleic Acids Research | 2006

Genome Snapshot: a new resource at the Saccharomyces Genome Database (SGD) presenting an overview of the Saccharomyces cerevisiae genome

Jodi E. Hirschman; Rama Balakrishnan; Karen R. Christie; Maria C. Costanzo; Selina S. Dwight; Stacia R. Engel; Dianna G. Fisk; Eurie L. Hong; Michael S. Livstone; Robert S. Nash; Julie Park; Rose Oughtred; Marek S. Skrzypek; Barry Starr; Chandra L. Theesfeld; Jennifer M. Williams; Rey Andrada; Gail Binkley; Qing Dong; Christopher Lane; Stuart R. Miyasato; Anand Sethuraman; Mark Schroeder; Mayank K. Thanawala; Shuai Weng; Kara Dolinski; David Botstein; J. Michael Cherry

Sequencing and annotation of the entire Saccharomyces cerevisiae genome has made it possible to gain a genome-wide perspective on yeast genes and gene products. To make this information available on an ongoing basis, the Saccharomyces Genome Database (SGD) () has created the Genome Snapshot (). The Genome Snapshot summarizes the current state of knowledge about the genes and chromosomal features of S.cerevisiae. The information is organized into two categories: (i) number of each type of chromosomal feature annotated in the genome and (ii) number and distribution of genes annotated to Gene Ontology terms. Detailed lists are accessible through SGDs Advanced Search tool (), and all the data presented on this page are available from the SGD ftp site ().


Nucleic Acids Research | 2007

Expanded protein information at SGD: new pages and proteome browser

Robert S. Nash; Shuai Weng; Benjamin C. Hitz; Rama Balakrishnan; Karen R. Christie; Maria C. Costanzo; Selina S. Dwight; Stacia R. Engel; Dianna G. Fisk; Jodi E. Hirschman; Eurie L. Hong; Michael S. Livstone; Rose Oughtred; Julie Park; Marek S. Skrzypek; Chandra L. Theesfeld; Gail Binkley; Qing Dong; Christopher Lane; Stuart R. Miyasato; Anand Sethuraman; Mark Schroeder; Kara Dolinski; David Botstein; J. Michael Cherry

The recent explosion in protein data generated from both directed small-scale studies and large-scale proteomics efforts has greatly expanded the quantity of available protein information and has prompted the Saccharomyces Genome Database (SGD; ) to enhance the depth and accessibility of protein annotations. In particular, we have expanded ongoing efforts to improve the integration of experimental information and sequence-based predictions and have redesigned the protein information web pages. A key feature of this redesign is the development of a GBrowse-derived interactive Proteome Browser customized to improve the visualization of sequence-based protein information. This Proteome Browser has enabled SGD to unify the display of hidden Markov model (HMM) domains, protein family HMMs, motifs, transmembrane regions, signal peptides, hydropathy plots and profile hits using several popular prediction algorithms. In addition, a physico-chemical properties page has been introduced to provide easy access to basic protein information. Improvements to the layout of the Protein Information page and integration of the Proteome Browser will facilitate the ongoing expansion of sequence-specific experimental information captured in SGD, including post-translational modifications and other user-defined annotations. Finally, SGD continues to improve upon the availability of genetic and physical interaction data in an ongoing collaboration with BioGRID by providing direct access to more than 82 000 manually-curated interactions.


Nucleic Acids Research | 2003

Saccharomyces Genome Database (SGD) provides biochemical and structural information for budding yeast proteins

Shuai Weng; Qing Dong; Rama Balakrishnan; Karen R. Christie; Maria C. Costanzo; Kara Dolinski; Selina S. Dwight; Stacia R. Engel; Dianna G. Fisk; Eurie L. Hong; Laurie Issel-Tarver; Anand Sethuraman; Chandra L. Theesfeld; Rey Andrada; Gail Binkley; Christopher Lane; Mark Schroeder; David Botstein; J. Michael Cherry

The Saccharomyces Genome Database (SGD: http://genome-www.stanford.edu/Saccharomyces/) has recently developed new resources to provide more complete information about proteins from the budding yeast Saccharomyces cerevisiae. The PDB Homologs page provides structural information from the Protein Data Bank (PDB) about yeast proteins and/or their homologs. SGD has also created a resource that utilizes the eMOTIF database for motif information about a given protein. A third new resource is the Protein Information page, which contains protein physical and chemical properties, such as molecular weight and hydropathicity scores, predicted from the translated ORF sequence.


Nucleic Acids Research | 2004

Fungal BLAST and Model Organism BLASTP Best Hits: new comparison resources at the Saccharomyces Genome Database (SGD).

Rama Balakrishnan; Karen R. Christie; Maria C. Costanzo; Kara Dolinski; Selina S. Dwight; Stacia R. Engel; Dianna G. Fisk; Jodi E. Hirschman; Eurie L. Hong; Robert S. Nash; Rose Oughtred; Marek S. Skrzypek; Chandra L. Theesfeld; Gail Binkley; Qing Dong; Christopher Lane; Anand Sethuraman; Shuai Weng; David Botstein; J. Michael Cherry

The Saccharomyces Genome Database (SGD; http://www.yeastgenome.org/) is a scientific database of gene, protein and genomic information for the yeast Saccharomyces cerevisiae. SGD has recently developed two new resources that facilitate nucleotide and protein sequence comparisons between S.cerevisiae and other organisms. The Fungal BLAST tool provides directed searches against all fungal nucleotide and protein sequences available from GenBank, divided into categories according to organism, status of completeness and annotation, and source. The Model Organism BLASTP Best Hits resource displays, for each S.cerevisiae protein, the single most similar protein from several model organisms and presents links to the database pages of those proteins, facilitating access to curated information about potential orthologs of yeast proteins.


Nature Neuroscience | 2016

Genome-wide prediction and functional characterization of the genetic basis of autism spectrum disorder

Arjun Krishnan; Ran Zhang; Victoria Yao; Chandra L. Theesfeld; Aaron K. Wong; Alicja Tadych; Natalia Volfovsky; Alan Packer; Alex E. Lash; Olga G. Troyanskaya

Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder with a strong genetic basis. Yet, only a small fraction of potentially causal genes—about 65 genes out of an estimated several hundred—are known with strong genetic evidence from sequencing studies. We developed a complementary machine-learning approach based on a human brain-specific gene network to present a genome-wide prediction of autism risk genes, including hundreds of candidates for which there is minimal or no prior genetic evidence. Our approach was validated in a large independent case–control sequencing study. Leveraging these genome-wide predictions and the brain-specific network, we demonstrated that the large set of ASD genes converges on a smaller number of key pathways and developmental stages of the brain. Finally, we identified likely pathogenic genes within frequent autism-associated copy-number variants and proposed genes and pathways that are likely mediators of ASD across multiple copy-number variants. All predictions and functional insights are available at http://asd.princeton.edu.


Genome Research | 2016

An extended set of yeast-based functional assays accurately identifies human disease mutations

Song Sun; Fan Yang; Guihong Tan; Michael Costanzo; Rose Oughtred; Jodi E. Hirschman; Chandra L. Theesfeld; Pritpal Bansal; Nidhi Sahni; Song Yi; Analyn Yu; Tanya Tyagi; Cathy Tie; David E. Hill; Marc Vidal; Brenda Andrews; Charles Boone; Kara Dolinski; Frederick P. Roth

We can now routinely identify coding variants within individual human genomes. A pressing challenge is to determine which variants disrupt the function of disease-associated genes. Both experimental and computational methods exist to predict pathogenicity of human genetic variation. However, a systematic performance comparison between them has been lacking. Therefore, we developed and exploited a panel of 26 yeast-based functional complementation assays to measure the impact of 179 variants (101 disease- and 78 non-disease-associated variants) from 22 human disease genes. Using the resulting reference standard, we show that experimental functional assays in a 1-billion-year diverged model organism can identify pathogenic alleles with significantly higher precision and specificity than current computational methods.


CSH Protocols | 2016

BioGRID: A Resource for Studying Biological Interactions in Yeast.

Rose Oughtred; Andrew Chatr-aryamontri; Bobby-Joe Breitkreutz; Christie S. Chang; Jennifer M. Rust; Chandra L. Theesfeld; Sven Heinicke; Ashton Breitkreutz; Daici Chen; Jodi E. Hirschman; Nadine Kolas; Michael S. Livstone; Julie Nixon; Lara O’Donnell; Lindsay Ramage; Andrew Winter; Teresa Reguly; Adnane Sellam; Chris Stark; Lorrie Boucher; Kara Dolinski; Mike Tyers

The Biological General Repository for Interaction Datasets (BioGRID) is a freely available public database that provides the biological and biomedical research communities with curated protein and genetic interaction data. Structured experimental evidence codes, an intuitive search interface, and visualization tools enable the discovery of individual gene, protein, or biological network function. BioGRID houses interaction data for the major model organism species--including yeast, nematode, fly, zebrafish, mouse, and human--with particular emphasis on the budding yeast Saccharomyces cerevisiae and the fission yeast Schizosaccharomyces pombe as pioneer eukaryotic models for network biology. BioGRID has achieved comprehensive curation coverage of the entire literature for these two major yeast models, which is actively maintained through monthly curation updates. As of September 2015, BioGRID houses approximately 335,400 biological interactions for budding yeast and approximately 67,800 interactions for fission yeast. BioGRID also supports an integrated posttranslational modification (PTM) viewer that incorporates more than 20,100 yeast phosphorylation sites curated through its sister database, the PhosphoGRID.

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