Gene Ranking based on Paths from Phenotypes to Genes on Knowledge Graph

Author:

Yamaguchi Atsuko1,Shin Jae-Moon2,Fujiwara Toyofumi2

Affiliation:

1. Tokyo City University, Japan

2. Database Center for Life Science, Japan

Funder

JSPS Kakenhi

Publisher

ACM

Reference10 articles.

1. Johannes Birgmeier , Maximilian Haeussler , Cole  A. Deisseroth , Ethan  H. Steinberg , Karthik  A. Jagadeesh , Alexander  J. Ratner , Harendra Guturu , Aaron  M. Wenger , Mark  E. Diekhans , Peter  D. Stenson , David  N. Cooper , Christopher Ré , Alan  H. Beggs , Jonathan  A. Bernstein , and Gill Bejerano . 2020. AMELIE speeds Mendelian diagnosis by matching patient phenotype and genotype to primary literature. Science Translational Medicine 12 ( 2020 ), eaau9113. Johannes Birgmeier, Maximilian Haeussler, Cole A. Deisseroth, Ethan H. Steinberg, Karthik A. Jagadeesh, Alexander J. Ratner, Harendra Guturu, Aaron M. Wenger, Mark E. Diekhans, Peter D. Stenson, David N. Cooper, Christopher Ré, Alan H. Beggs, Jonathan A. Bernstein, and Gill Bejerano. 2020. AMELIE speeds Mendelian diagnosis by matching patient phenotype and genotype to primary literature. Science Translational Medicine 12 (2020), eaau9113.

2. The Semanticscience Integrated Ontology (SIO) for biomedical research and knowledge discovery

3. PubCaseFinder: A Case-Report-Based, Phenotype-Driven Differential-Diagnosis System for Rare Diseases

4. Michael  M. Gottlieb , David  J. Arenillas , Savanie Maithripala , Zachary  D. Maurer , Maja Tarailo Graovac , Linlea Armstrong , Millan Patel , Clara van Karnebeek , and Wyeth  W. Wasserman . 2015. GeneYenta: a phenotype-based rare disease case matching tool based on online dating algorithms for the acceleration of exome interpretation. Human mutation 36, 4 ( 2015 ), 432–438. Michael M. Gottlieb, David J. Arenillas, Savanie Maithripala, Zachary D. Maurer, Maja Tarailo Graovac, Linlea Armstrong, Millan Patel, Clara van Karnebeek, and Wyeth W. Wasserman. 2015. GeneYenta: a phenotype-based rare disease case matching tool based on online dating algorithms for the acceleration of exome interpretation. Human mutation 36, 4 (2015), 432–438.

5. Mayumi Kamada , Toshiaki Katayama , Shuichi Kawashima , Ryosuke Kojima , Masahiko Nakatsui , and Yasushi Okuno . 2019. Med2RDF: Semantic Biomedical Knowledge-base and APIs for the Clinical Genome Medicine . In Proceedings of 12th International Conference on Semantic Web Applications and Tools for Health Care and Life Sciences(SWAT4HCLS 2019 ), Ronald Cornet and Andra Waagmeester (Eds.). CEUR Workshop Proceedings, Edinburgh, Scotland , 161–162. http://ceur-ws.org/Vol-2849/paper-31.pdf Mayumi Kamada, Toshiaki Katayama, Shuichi Kawashima, Ryosuke Kojima, Masahiko Nakatsui, and Yasushi Okuno. 2019. Med2RDF: Semantic Biomedical Knowledge-base and APIs for the Clinical Genome Medicine. In Proceedings of 12th International Conference on Semantic Web Applications and Tools for Health Care and Life Sciences(SWAT4HCLS 2019), Ronald Cornet and Andra Waagmeester (Eds.). CEUR Workshop Proceedings, Edinburgh, Scotland, 161–162. http://ceur-ws.org/Vol-2849/paper-31.pdf

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Integrating Knowledge Graphs for Enhanced Drilling Accident Retrieval and Risk Prediction in China's Oil and Gas Industry;2024 IEEE 6th Advanced Information Management, Communicates, Electronic and Automation Control Conference (IMCEC);2024-05-24

2. KG-Hub—building and exchanging biological knowledge graphs;Bioinformatics;2023-06-30

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3