Literature DB >> 24939151

Literome: PubMed-scale genomic knowledge base in the cloud.

Hoifung Poon1, Chris Quirk1, Charlie DeZiel1, David Heckerman1.   

Abstract

MOTIVATION: Advances in sequencing technology have led to an exponential growth of genomics data, yet it remains a formidable challenge to interpret such data for identifying disease genes and drug targets. There has been increasing interest in adopting a systems approach that incorporates prior knowledge such as gene networks and genotype-phenotype associations. The majority of such knowledge resides in text such as journal publications, which has been undergoing its own exponential growth. It has thus become a significant bottleneck to identify relevant knowledge for genomic interpretation as well as to keep up with new genomics findings.
RESULTS: In the Literome project, we have developed an automatic curation system to extract genomic knowledge from PubMed articles and made this knowledge available in the cloud with a Web site to facilitate browsing, searching and reasoning. Currently, Literome focuses on two types of knowledge most pertinent to genomic medicine: directed genic interactions such as pathways and genotype-phenotype associations. Users can search for interacting genes and the nature of the interactions, as well as diseases and drugs associated with a single nucleotide polymorphism or gene. Users can also search for indirect connections between two entities, e.g. a gene and a disease might be linked because an interacting gene is associated with a related disease.
AVAILABILITY AND IMPLEMENTATION: Literome is freely available at literome.azurewebsites.net. Download for non-commercial use is available via Web services.
© The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

Mesh:

Year:  2014        PMID: 24939151     DOI: 10.1093/bioinformatics/btu383

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  25 in total

Review 1.  Sex and gender differences and biases in artificial intelligence for biomedicine and healthcare.

Authors:  Davide Cirillo; Silvina Catuara-Solarz; Czuee Morey; Emre Guney; Laia Subirats; Simona Mellino; Annalisa Gigante; Alfonso Valencia; María José Rementeria; Antonella Santuccione Chadha; Nikolaos Mavridis
Journal:  NPJ Digit Med       Date:  2020-06-01

Review 2.  Genetic Testing and Tissue Banking for Personalized Oncology: Analytical and Institutional Factors.

Authors:  George Miles; James Rae; Suresh S Ramalingam; John Pfeifer
Journal:  Semin Oncol       Date:  2015-07-14       Impact factor: 4.929

3.  A basal stem cell signature identifies aggressive prostate cancer phenotypes.

Authors:  Bryan A Smith; Artem Sokolov; Vladislav Uzunangelov; Robert Baertsch; Yulia Newton; Kiley Graim; Colleen Mathis; Donghui Cheng; Joshua M Stuart; Owen N Witte
Journal:  Proc Natl Acad Sci U S A       Date:  2015-10-12       Impact factor: 11.205

4.  Notch signaling activation induces cell death in MAPKi-resistant melanoma cells.

Authors:  Dareen M Mikheil; Kirthana Prabhakar; Ayyan Arshad; Carlos I Rodriguez; Michael A Newton; Vijayasaradhi Setaluri
Journal:  Pigment Cell Melanoma Res       Date:  2019-02-03       Impact factor: 4.693

5.  Identifying digenic disease genes via machine learning in the Undiagnosed Diseases Network.

Authors:  Souhrid Mukherjee; Joy D Cogan; John H Newman; John A Phillips; Rizwan Hamid; Jens Meiler; John A Capra
Journal:  Am J Hum Genet       Date:  2021-09-15       Impact factor: 11.025

6.  GeneDive: A gene interaction search and visualization tool to facilitate precision medicine.

Authors:  Paul Previde; Brook Thomas; Mike Wong; Emily K Mallory; Dragutin Petkovic; Russ B Altman; Anagha Kulkarni
Journal:  Pac Symp Biocomput       Date:  2018

7.  Integrative Analysis Identifies Four Molecular and Clinical Subsets in Uveal Melanoma.

Authors:  A Gordon Robertson; Juliann Shih; Christina Yau; Ewan A Gibb; Junna Oba; Karen L Mungall; Julian M Hess; Vladislav Uzunangelov; Vonn Walter; Ludmila Danilova; Tara M Lichtenberg; Melanie Kucherlapati; Patrick K Kimes; Ming Tang; Alexander Penson; Ozgun Babur; Rehan Akbani; Christopher A Bristow; Katherine A Hoadley; Lisa Iype; Matthew T Chang; Andrew D Cherniack; Christopher Benz; Gordon B Mills; Roel G W Verhaak; Klaus G Griewank; Ina Felau; Jean C Zenklusen; Jeffrey E Gershenwald; Lynn Schoenfield; Alexander J Lazar; Mohamed H Abdel-Rahman; Sergio Roman-Roman; Marc-Henri Stern; Colleen M Cebulla; Michelle D Williams; Martine J Jager; Sarah E Coupland; Bita Esmaeli; Cyriac Kandoth; Scott E Woodman
Journal:  Cancer Cell       Date:  2017-08-14       Impact factor: 31.743

8.  Knowledge bases and software support for variant interpretation in precision oncology.

Authors:  Florian Borchert; Andreas Mock; Aurelie Tomczak; Jonas Hügel; Samer Alkarkoukly; Alexander Knurr; Anna-Lena Volckmar; Albrecht Stenzinger; Peter Schirmacher; Jürgen Debus; Dirk Jäger; Thomas Longerich; Stefan Fröhling; Roland Eils; Nina Bougatf; Ulrich Sax; Matthieu-P Schapranow
Journal:  Brief Bioinform       Date:  2021-11-05       Impact factor: 11.622

9.  Down-regulation of BCL2L13 renders poor prognosis in clear cell and papillary renal cell carcinoma.

Authors:  Fei Meng; Luojin Zhang; Mingjun Zhang; Kaiqin Ye; Wei Guo; Yu Liu; Wulin Yang; Zhimin Zhai; Hongzhi Wang; Jun Xiao; Haiming Dai
Journal:  Cancer Cell Int       Date:  2021-06-30       Impact factor: 5.722

10.  Search and visualization of gene-drug-disease interactions for pharmacogenomics and precision medicine research using GeneDive.

Authors:  Mike Wong; Paul Previde; Jack Cole; Brook Thomas; Nayana Laxmeshwar; Emily Mallory; Jake Lever; Dragutin Petkovic; Russ B Altman; Anagha Kulkarni
Journal:  J Biomed Inform       Date:  2021-03-16       Impact factor: 8.000

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