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Dive into the research topics where Angie S. Hinrichs is active.

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Featured researches published by Angie S. Hinrichs.


Nucleic Acids Research | 2006

The UCSC genome browser database: update 2007

Robert M. Kuhn; Donna Karolchik; Ann S. Zweig; Heather Trumbower; Daryl J. Thomas; Archana Thakkapallayil; Charles W. Sugnet; Mario Stanke; Kayla E. Smith; Adam Siepel; Kate R. Rosenbloom; Brooke Rhead; Brian J. Raney; Andrew A. Pohl; Jakob Skou Pedersen; Fan Hsu; Angie S. Hinrichs; Rachel A. Harte; Mark Diekhans; Hiram Clawson; Gill Bejerano; Galt P. Barber; Robert Baertsch; David Haussler; William Kent

The UCSC Genome Browser Database (GBD, http://genome.ucsc.edu) is a publicly available collection of genome assembly sequence data and integrated annotations for a large number of organisms, including extensive comparative-genomic resources. In the past year, 13 new genome assemblies have been added, including two important primate species, orangutan and marmoset, bringing the total to 46 assemblies for 24 different vertebrates and 39 assemblies for 22 different invertebrate animals. The GBD datasets may be viewed graphically with the UCSC Genome Browser, which uses a coordinate-based display system allowing users to juxtapose a wide variety of data. These data include all mRNAs from GenBank mapped to all organisms, RefSeq alignments, gene predictions, regulatory elements, gene expression data, repeats, SNPs and other variation data, as well as pairwise and multiple-genome alignments. A variety of other bioinformatics tools are also provided, including BLAT, the Table Browser, the Gene Sorter, the Proteome Browser, VisiGene and Genome Graphs.


Nucleic Acids Research | 2012

The UCSC Genome Browser database: extensions and updates 2011

Timothy R. Dreszer; Donna Karolchik; Ann S. Zweig; Angie S. Hinrichs; Brian J. Raney; Robert M. Kuhn; Laurence R. Meyer; Matthew C. Wong; Cricket A. Sloan; Kate R. Rosenbloom; Greg Roe; Brooke Rhead; Andy Pohl; Venkat S. Malladi; Chin H. Li; Katrina Learned; Vanessa M. Kirkup; Fan Hsu; Rachel A. Harte; Luvina Guruvadoo; Mary Goldman; Belinda Giardine; Pauline A. Fujita; Mark Diekhans; Melissa S. Cline; Hiram Clawson; Galt P. Barber; David Haussler; W. James Kent

The University of California Santa Cruz Genome Browser (http://genome.ucsc.edu) offers online public access to a growing database of genomic sequence and annotations for a wide variety of organisms. The Browser is an integrated tool set for visualizing, comparing, analyzing and sharing both publicly available and user-generated genomic data sets. In the past year, the local database has been updated with four new species assemblies, and we anticipate another four will be released by the end of 2011. Further, a large number of annotation tracks have been either added, updated by contributors, or remapped to the latest human reference genome. Among these are new phenotype and disease annotations, UCSC genes, and a major dbSNP update, which required new visualization methods. Growing beyond the local database, this year we have introduced ‘track data hubs’, which allow the Genome Browser to provide access to remotely located sets of annotations. This feature is designed to significantly extend the number and variety of annotation tracks that are publicly available for visualization and analysis from within our site. We have also introduced several usability features including track search and a context-sensitive menu of options available with a right-click anywhere on the Browsers image.


Proceedings of the National Academy of Sciences of the United States of America | 2003

Evolution's cauldron: Duplication, deletion, and rearrangement in the mouse and human genomes

W. James Kent; Robert Baertsch; Angie S. Hinrichs; Webb Miller; David Haussler

This study examines genomic duplications, deletions, and rearrangements that have happened at scales ranging from a single base to complete chromosomes by comparing the mouse and human genomes. From whole-genome sequence alignments, 344 large (>100-kb) blocks of conserved synteny are evident, but these are further fragmented by smaller-scale evolutionary events. Excluding transposon insertions, on average in each megabase of genomic alignment we observe two inversions, 17 duplications (five tandem or nearly tandem), seven transpositions, and 200 deletions of 100 bases or more. This includes 160 inversions and 75 duplications or transpositions of length >100 kb. The frequencies of these smaller events are not substantially higher in finished portions in the assembly. Many of the smaller transpositions are processed pseudogenes; we define a “syntenic” subset of the alignments that excludes these and other small-scale transpositions. These alignments provide evidence that ≈2% of the genes in the human/mouse common ancestor have been deleted or partially deleted in the mouse. There also appears to be slightly less nontransposon-induced genome duplication in the mouse than in the human lineage. Although some of the events we detect are possibly due to misassemblies or missing data in the current genome sequence or to the limitations of our methods, most are likely to represent genuine evolutionary events. To make these observations, we developed new alignment techniques that can handle large gaps in a robust fashion and discriminate between orthologous and paralogous alignments.


Nature | 2007

Discovery of functional elements in 12 Drosophila genomes using evolutionary signatures

Alexander Stark; Michael F. Lin; Pouya Kheradpour; Jakob Skou Pedersen; Leopold Parts; Joseph W. Carlson; Madeline A. Crosby; Matthew D. Rasmussen; Sushmita Roy; Ameya N. Deoras; J. Graham Ruby; Julius Brennecke; Harvard FlyBase curators; Berkeley Drosophila Genome; Emily Hodges; Angie S. Hinrichs; Anat Caspi; Benedict Paten; Seung-Won Park; Mira V. Han; Morgan L. Maeder; Benjamin J. Polansky; Bryanne E. Robson; Stein Aerts; Jacques van Helden; Bassem A. Hassan; Donald G. Gilbert; Deborah A. Eastman; Michael D. Rice; Michael Weir

Sequencing of multiple related species followed by comparative genomics analysis constitutes a powerful approach for the systematic understanding of any genome. Here, we use the genomes of 12 Drosophila species for the de novo discovery of functional elements in the fly. Each type of functional element shows characteristic patterns of change, or ‘evolutionary signatures’, dictated by its precise selective constraints. Such signatures enable recognition of new protein-coding genes and exons, spurious and incorrect gene annotations, and numerous unusual gene structures, including abundant stop-codon readthrough. Similarly, we predict non-protein-coding RNA genes and structures, and new microRNA (miRNA) genes. We provide evidence of miRNA processing and functionality from both hairpin arms and both DNA strands. We identify several classes of pre- and post-transcriptional regulatory motifs, and predict individual motif instances with high confidence. We also study how discovery power scales with the divergence and number of species compared, and we provide general guidelines for comparative studies.


Nucleic Acids Research | 2014

The UCSC Genome Browser database: 2014 update

Donna Karolchik; Galt P. Barber; Jonathan Casper; Hiram Clawson; Melissa S. Cline; Mark Diekhans; Timothy R. Dreszer; Pauline A. Fujita; Luvina Guruvadoo; Maximilian Haeussler; Rachel A. Harte; Steven G. Heitner; Angie S. Hinrichs; Katrina Learned; Brian T. Lee; Chin H. Li; Brian J. Raney; Brooke Rhead; Kate R. Rosenbloom; Cricket A. Sloan; Matthew L. Speir; Ann S. Zweig; David Haussler; Robert M. Kuhn; W. James Kent

The University of California Santa Cruz (UCSC) Genome Browser (http://genome.ucsc.edu) offers online public access to a growing database of genomic sequence and annotations for a large collection of organisms, primarily vertebrates, with an emphasis on the human and mouse genomes. The Browser’s web-based tools provide an integrated environment for visualizing, comparing, analysing and sharing both publicly available and user-generated genomic data sets. As of September 2013, the database contained genomic sequence and a basic set of annotation ‘tracks’ for ∼90 organisms. Significant new annotations include a 60-species multiple alignment conservation track on the mouse, updated UCSC Genes tracks for human and mouse, and several new sets of variation and ENCODE data. New software tools include a Variant Annotation Integrator that returns predicted functional effects of a set of variants uploaded as a custom track, an extension to UCSC Genes that displays haplotype alleles for protein-coding genes and an expansion of data hubs that includes the capability to display remotely hosted user-provided assembly sequence in addition to annotation data. To improve European access, we have added a Genome Browser mirror (http://genome-euro.ucsc.edu) hosted at Bielefeld University in Germany.


Nucleic Acids Research | 2007

The UCSC Genome Browser Database: 2008 update

Donna Karolchik; Robert M. Kuhn; Robert Baertsch; Galt P. Barber; Hiram Clawson; Mark Diekhans; Belinda Giardine; Rachel A. Harte; Angie S. Hinrichs; Fan Hsu; K. M. Kober; Webb Miller; Jakob Skou Pedersen; Andy Pohl; Brian J. Raney; Brooke Rhead; Kate R. Rosenbloom; Kayla E. Smith; Mario Stanke; Archana Thakkapallayil; Heather Trumbower; Ting Wang; Ann S. Zweig; David Haussler; William Kent

The University of California, Santa Cruz, Genome Browser Database (GBD) provides integrated sequence and annotation data for a large collection of vertebrate and model organism genomes. Seventeen new assemblies have been added to the database in the past year, for a total coverage of 19 vertebrate and 21 invertebrate species as of September 2007. For each assembly, the GBD contains a collection of annotation data aligned to the genomic sequence. Highlights of this year’s additions include a 28-species human-based vertebrate conservation annotation, an enhanced UCSC Genes set, and more human variation, MGC, and ENCODE data. The database is optimized for fast interactive performance with a set of web-based tools that may be used to view, manipulate, filter and download the annotation data. New toolset features include the Genome Graphs tool for displaying genome-wide data sets, session saving and sharing, better custom track management, expanded Genome Browser configuration options and a Genome Browser wiki site. The downloadable GBD data, the companion Genome Browser toolset and links to documentation and related information can be found at: http://genome.ucsc.edu/. INTRODUCTION Fundamental to expanding our knowledge of how the human body works in health and in disease is the capability to access and share data produced through experimentation and computational analysis. The University of California, Santa Cruz (UCSC) Genome Browser Database (GBD) (http://genome.ucsc.edu) (1) provides a common repository for genomic annotation data—including comparative genomics, genes and gene predictions; mRNA and EST alignments; and expression, regulation, variation and assembly data—and robust, flexible tools for viewing, comparing, distributing and analyzing the information. Produced and maintained by the Genome Bioinformatics Group at the UCSC Center for Biomolecular Science and Engineering, the GBD focuses primarily on vertebrate and model organism genomes, with an emphasis on comparative genomics analysis. As of September 2007 the GBD contains data for 11 mammalian species including human, mouse, rat, chimpanzee, rhesus macaque, horse, cow, cat, dog, opossum and platypus; 8 other vertebrates: chicken, lizard (Anolis carolinensis), frog (Xenopus tropicalis), zebrafish, fugu, tetraodon, medaka and stickleback; and 21 invertebrates including 11 flies, honeybee, Anopheles mosquito, five worms, one yeast (Saccharomyces cerevisiae) and two deuterostomes—purple sea urchin and sea squirt. For many of the organisms, more than one assembly is provided, and several older archived assemblies may be *To whom correspondence should be addressed. Tel: +1 831 459 1544; Fax: +1 831 459 1809; Email: [email protected] University of California, Santa Cruz, Genome Browser Database (GBD) provides integrated sequence and annotation data for a large collection of vertebrate and model organism genomes. Seventeen new assemblies have been added to the database in the past year, for a total coverage of 19 vertebrate and 21 invertebrate species as of September 2007. For each assembly, the GBD contains a collection of annotation data aligned to the genomic sequence. Highlights of this years additions include a 28-species human-based vertebrate conservation annotation, an enhanced UCSC Genes set, and more human variation, MGC, and ENCODE data. The database is optimized for fast interactive performance with a set of web-based tools that may be used to view, manipulate, filter and download the annotation data. New toolset features include the Genome Graphs tool for displaying genome-wide data sets, session saving and sharing, better custom track management, expanded Genome Browser configuration options and a Genome Browser wiki site. The downloadable GBD data, the companion Genome Browser toolset and links to documentation and related information can be found at: http://genome.ucsc.edu/.


Nucleic Acids Research | 2015

The UCSC Genome Browser database: 2015 update

Kate R. Rosenbloom; Joel Armstrong; Galt P. Barber; Jonathan Casper; Hiram Clawson; Mark Diekhans; Timothy R. Dreszer; Pauline A. Fujita; Luvina Guruvadoo; Maximilian Haeussler; Rachel A. Harte; Steven G. Heitner; Glenn Hickey; Angie S. Hinrichs; Robert Hubley; Donna Karolchik; Katrina Learned; Brian T. Lee; Chin H. Li; Karen H. Miga; Ngan Nguyen; Benedict Paten; Brian J. Raney; Arian Smit; Matthew L. Speir; Ann S. Zweig; David Haussler; Robert M. Kuhn; W. James Kent

Launched in 2001 to showcase the draft human genome assembly, the UCSC Genome Browser database (http://genome.ucsc.edu) and associated tools continue to grow, providing a comprehensive resource of genome assemblies and annotations to scientists and students worldwide. Highlights of the past year include the release of a browser for the first new human genome reference assembly in 4 years in December 2013 (GRCh38, UCSC hg38), a watershed comparative genomics annotation (100-species multiple alignment and conservation) and a novel distribution mechanism for the browser (GBiB: Genome Browser in a Box). We created browsers for new species (Chinese hamster, elephant shark, minke whale), ‘mined the web’ for DNA sequences and expanded the browser display with stacked color graphs and region highlighting. As our user community increasingly adopts the UCSC track hub and assembly hub representations for sharing large-scale genomic annotation data sets and genome sequencing projects, our menu of public data hubs has tripled.


Nucleic Acids Research | 2010

ENCODE whole-genome data in the UCSC Genome Browser

Kate R. Rosenbloom; Timothy R. Dreszer; Michael Pheasant; Galt P. Barber; Laurence R. Meyer; Andy Pohl; Brian J. Raney; Ting Wang; Angie S. Hinrichs; Ann S. Zweig; Pauline A. Fujita; Katrina Learned; Brooke Rhead; Kayla E. Smith; Robert M. Kuhn; Donna Karolchik; David Haussler; W. James Kent

The Encyclopedia of DNA Elements (ENCODE) project is an international consortium of investigators funded to analyze the human genome with the goal of producing a comprehensive catalog of functional elements. The ENCODE Data Coordination Center at The University of California, Santa Cruz (UCSC) is the primary repository for experimental results generated by ENCODE investigators. These results are captured in the UCSC Genome Bioinformatics database and download server for visualization and data mining via the UCSC Genome Browser and companion tools (Rhead et al. The UCSC Genome Browser Database: update 2010, in this issue). The ENCODE web portal at UCSC (http://encodeproject.org or http://genome.ucsc.edu/ENCODE) provides information about the ENCODE data and convenient links for access.


Bioinformatics | 2010

BigWig and BigBed

William Kent; Ann S. Zweig; Galt P. Barber; Angie S. Hinrichs; Donna Karolchik

Summary: BigWig and BigBed files are compressed binary indexed files containing data at several resolutions that allow the high-performance display of next-generation sequencing experiment results in the UCSC Genome Browser. The visualization is implemented using a multi-layered software approach that takes advantage of specific capabilities of web-based protocols and Linux and UNIX operating systems files, R trees and various indexing and compression tricks. As a result, only the data needed to support the current browser view is transmitted rather than the entire file, enabling fast remote access to large distributed data sets. Availability and implementation: Binaries for the BigWig and BigBed creation and parsing utilities may be downloaded at http://hgdownload.cse.ucsc.edu/admin/exe/linux.x86_64/. Source code for the creation and visualization software is freely available for non-commercial use at http://hgdownload.cse.ucsc.edu/admin/jksrc.zip, implemented in C and supported on Linux. The UCSC Genome Browser is available at http://genome.ucsc.edu Contact: [email protected] Supplementary information: Supplementary byte-level details of the BigWig and BigBed file formats are available at Bioinformatics online. For an in-depth description of UCSC data file formats and custom tracks, see http://genome.ucsc.edu/FAQ/FAQformat.html and http://genome.ucsc.edu/goldenPath/help/hgTracksHelp.html


Nucleic Acids Research | 2016

The UCSC Genome Browser database: 2016 update.

Matthew L. Speir; Ann S. Zweig; Kate R. Rosenbloom; Brian J. Raney; Benedict Paten; Parisa Nejad; Brian T. Lee; Katrina Learned; Donna Karolchik; Angie S. Hinrichs; Steven G. Heitner; Rachel A. Harte; Maximilian Haeussler; Luvina Guruvadoo; Pauline A. Fujita; Christopher Eisenhart; Mark Diekhans; Hiram Clawson; Jonathan Casper; Galt P. Barber; David Haussler; Robert M. Kuhn; W. James Kent

For the past 15 years, the UCSC Genome Browser (http://genome.ucsc.edu/) has served the international research community by offering an integrated platform for viewing and analyzing information from a large database of genome assemblies and their associated annotations. The UCSC Genome Browser has been under continuous development since its inception with new data sets and software features added frequently. Some release highlights of this year include new and updated genome browsers for various assemblies, including bonobo and zebrafish; new gene annotation sets; improvements to track and assembly hub support; and a new interactive tool, the “Data Integrator”, for intersecting data from multiple tracks. We have greatly expanded the data sets available on the most recent human assembly, hg38/GRCh38, to include updated gene prediction sets from GENCODE, more phenotype- and disease-associated variants from ClinVar and ClinGen, more genomic regulatory data, and a new multiple genome alignment.

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David Haussler

University of California

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W. James Kent

University of California

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Ann S. Zweig

University of California

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Brian J. Raney

University of California

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Hiram Clawson

University of California

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Robert M. Kuhn

University of California

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Galt P. Barber

University of California

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Mark Diekhans

University of California

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