• Documents
  • Authors
  • Tables
  • Log in
  • Sign up
  • MetaCart
  • DMCA
  • Donate

CiteSeerX logo

Tools

Sorted by:
Try your query at:
Semantic Scholar Scholar Academic
Google Bing DBLP
Results 1 - 10 of 26
Next 10 →

UTGB Toolkit for Personalized Genome Browsers

by Taro L. Saito, Jun Yoshimura, Shin Sasaki, Budrul Ahsan, Reginaldo Kuroshu, Shinichi Morishita
"... The advent of high-throughput DNA sequencers has increased the pace of collecting enormous amounts of genomic information, yielding billions of nucleotides on a weekly basis. This advance represents an improvement of two orders of magnitude over traditional Sanger sequencers in terms of the number o ..."
Abstract - Add to MetaCart
of Tokyo Genome Browser) Toolkit is designed to meet three major requirements for personalization of genome browsers: easy installation of the system with minimum efforts, browsing locally stored data, and rapid interactive design of web interfaces tailored to individual needs. The UTGB Toolkit is licensed

Genome analysis

by Taro L. Saito, Jun Yoshimura, Shin Sasaki, Budrul Ahsan, Atsushi Sasaki, Reginaldo Kuroshu, Shinichi Morishita , 2009
"... UTGB toolkit for personalized genome browsers ..."
Abstract - Cited by 1 (0 self) - Add to MetaCart
UTGB toolkit for personalized genome browsers

The personal genome browser: visualizing functions of genetic variants

by Liran Juan, Mingxiang Teng, Tianyi Zang, Yafeng Hao, Zhenxing Wang, Chengwu Yan, Yongzhuang Liu, Jie Li, Tianjiao Zhang, Yadong Wang - Nucleic Acids Res , 2014
"... Advances in high-throughput sequencing technolo-gies have brought us into the individual genome era. Projects such as the 1000 Genomes Project have led the individual genome sequencing to be-come more and more popular. How to visualize, anal-yse and annotate individual genomes with knowl-edge bases ..."
Abstract - Cited by 4 (2 self) - Add to MetaCart
to support genome studies and per-sonalized healthcare is still a big challenge. The Personal Genome Browser (PGB) is developed to provide comprehensive functional annotation and visualization for individual genomes based on the genetic–molecular–phenotypic model. Investigators can easily view individual

Family Genome Browser: Visualizing Genomes with Pedigree In- formation

by Genome Analysis, Liran Juan, Yongzhuang Liu, Yongtian Wang, Mingxiang Teng, Tianyi Zang
"... Motivation: Families with inherited diseases are widely used in Mendelian/complex disease studies. Owing to the advances in high-throughput sequencing technologies, family genome sequencing becomes more and more prevalent. Visualizing family genomes can greatly facilitate human genetics studies and ..."
Abstract - Add to MetaCart
and personalized medicine. However, due to the complex genetic relationships and high similari-ties among genomes of consanguineous family members, family genomes are difficult to be visualized in traditional genome visuali-zation framework. How to visualize the family genome variants and their functions

User Interface Toolkit for Ubiquitous TV

by Javier Burón Fernández, Konstantinos Chorianopoulos, Enrique García Salcines, De Castro Lozano, Beatriz Sainz, De Abajo
"... The wide adoption of small and powerful mobile computers, such as smart phones and tablets, has raised the opportunity to employ them in multi-user and multi-device iTV scenarios. In particular, the standardization of HTML5 and the increase of cloud services have made the web browser a suitable tool ..."
Abstract - Add to MetaCart
The wide adoption of small and powerful mobile computers, such as smart phones and tablets, has raised the opportunity to employ them in multi-user and multi-device iTV scenarios. In particular, the standardization of HTML5 and the increase of cloud services have made the web browser a suitable

Genome analysis Advance Access publication December 6, 2012 ChromoZoom: a flexible, fluid, web-based genome browser

by Theodore R. Pak, Frederick P. Roth, Alfonso Valencia , 2012
"... Summary: Current web-based genome browsers require repetitious user input to scroll over long distances, alter the drawing density of elements or zoom through multiple orders of magnitude. Generally, either the server or the client is responsible for the majority of data processing, resulting in eit ..."
Abstract - Add to MetaCart
Summary: Current web-based genome browsers require repetitious user input to scroll over long distances, alter the drawing density of elements or zoom through multiple orders of magnitude. Generally, either the server or the client is responsible for the majority of data processing, resulting

Personal Inquiry: Lessons Learned

by S. Anastopoulou, M. Wright, M. Sharples, S. Ainsworth, C. Crook, B. Norton
"... The paper describes a school trial in secondary to school to explore how version 1 of the PI Toolkit helped students to perform a personally relevant scientific inquiry in a science classroom and at home. Over a three-week period (nine lessons), twenty one 13-14 year old students in an inner city sc ..."
Abstract - Add to MetaCart
The paper describes a school trial in secondary to school to explore how version 1 of the PI Toolkit helped students to perform a personally relevant scientific inquiry in a science classroom and at home. Over a three-week period (nine lessons), twenty one 13-14 year old students in an inner city

Superimposed Information for the Internet

by David Maier, Lois Delcambre , 1999
"... Introduction It has existed for several millennia, in the form of commentaries on religious books, law and literature. We see it today in concordances, citation indexes and genome maps. You probably have created some of it, as a bookmark file in your web browser. The "it" we refer to is ..."
Abstract - Cited by 48 (8 self) - Add to MetaCart
Introduction It has existed for several millennia, in the form of commentaries on religious books, law and literature. We see it today in concordances, citation indexes and genome maps. You probably have created some of it, as a bookmark file in your web browser. The "it" we refer

RESEARCH ARTICLE Low-Frequency IL23R Coding Variant Associated with Crohn’s Disease Susceptibility in Japanese Subjects Identified by Personal Genomics Analysis

by Kei Onodera, Yoshiaki Arimura, Hiroyuki Isshiki, Kentaro Kawakami, Kanna Nagaishi, Kentaro Yamashita, Eiichiro Yamamoto, Takeshi Niinuma, Yasuyoshi Naishiro, Hiromu Suzuki, Kohzoh Imai, Yasuhisa Shinomura , 1371
"... Background The common disease-common variant hypothesis is insufficient to explain the complexities of Crohn’s disease (CD) genetics; therefore, rare variants are expected to be important in the disease. We explored rare variants associated with susceptibility to CD in Japanese individuals by person ..."
Abstract - Add to MetaCart
by personal genomic analysis. Methods Two-step analyses were performed. The first step was a trio analysis with whole-exome sequence (WES) analysis and the second was a follow-up case-control association study. TheWES analysis pipeline comprised Burrows-Wheeler Aligner, Picard, Genome Analysis Toolkit

VMD: a community annotation database for oomycetes and microbial genomes

by Sucheta Tripathy, Varun N. P, Bing Fang, Fidel Salas, Brett M. Tyler - Nucleic Acids Res , 2006
"... The VBI Microbial Database (VMD) is a database system designed to host a range of microbial genome sequences. At present, the database contains genome sequence and annotation data of two plant pathogens Phytophthora sojae and Phytophthora ramorum. With the completion of the draft genome sequences of ..."
Abstract - Cited by 4 (0 self) - Add to MetaCart
created an easy-to-use genome browser to view the genome sequence data, which opens to detailed annotation pages for each gene model. A community annotation interface is available for registered community members to add or edit annotations. There are 1600 gene models for P.sojae and 700 models for P
Next 10 →
Results 1 - 10 of 26
Powered by: Apache Solr
  • About CiteSeerX
  • Submit and Index Documents
  • Privacy Policy
  • Help
  • Data
  • Source
  • Contact Us

Developed at and hosted by The College of Information Sciences and Technology

© 2007-2019 The Pennsylvania State University