Phenopolis: an open platform for harmonization and analysis of genetic and phenotypic data
- PMID: 28334266
- DOI: 10.1093/bioinformatics/btx147
Phenopolis: an open platform for harmonization and analysis of genetic and phenotypic data
Abstract
Summary: Phenopolis is an open-source web server providing an intuitive interface to genetic and phenotypic databases. It integrates analysis tools such as variant filtering and gene prioritization based on phenotype. The Phenopolis platform will accelerate clinical diagnosis, gene discovery and encourage wider adoption of the Human Phenotype Ontology in the study of rare genetic diseases.
Availability and implementation: A demo of the website is available at https://phenopolis.github.io . If you wish to install a local copy, source code and installation instruction are available at https://github.com/phenopolis . The software is implemented using Python, MongoDB, HTML/Javascript and various bash shell scripts.
Contact: n.pontikos@ucl.ac.uk.
Supplementary information: Supplementary data are available at Bioinformatics online.
© The Author (2017). Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com
Similar articles
-
Pheno4J: a gene to phenotype graph database.Bioinformatics. 2017 Oct 15;33(20):3317-3319. doi: 10.1093/bioinformatics/btx397. Bioinformatics. 2017. PMID: 28633344
-
Novel phenotype-disease matching tool for rare genetic diseases.Genet Med. 2019 Feb;21(2):339-346. doi: 10.1038/s41436-018-0050-4. Epub 2018 Jun 12. Genet Med. 2019. PMID: 29895857
-
A clinical knowledge graph-based framework to prioritize candidate genes for facilitating diagnosis of Mendelian diseases and rare genetic conditions.BMC Bioinformatics. 2025 Mar 14;26(1):82. doi: 10.1186/s12859-025-06096-2. BMC Bioinformatics. 2025. PMID: 40087567 Free PMC article.
-
Genetic Modifiers and Rare Mendelian Disease.Genes (Basel). 2020 Feb 25;11(3):239. doi: 10.3390/genes11030239. Genes (Basel). 2020. PMID: 32106447 Free PMC article. Review.
-
Harmonising phenomics information for a better interoperability in the rare disease field.Eur J Med Genet. 2018 Nov;61(11):706-714. doi: 10.1016/j.ejmg.2018.01.013. Epub 2018 Feb 7. Eur J Med Genet. 2018. PMID: 29425702 Review.
Cited by
-
Clinical and Genetic Characteristics of 15 Affected Patients From 12 Japanese Families with GUCY2D-Associated Retinal Disorder.Transl Vis Sci Technol. 2020 May 11;9(6):2. doi: 10.1167/tvst.9.6.2. eCollection 2020 May. Transl Vis Sci Technol. 2020. PMID: 32821499 Free PMC article.
-
ENIGMA HALFpipe: Interactive, reproducible, and efficient analysis for resting-state and task-based fMRI data.Hum Brain Mapp. 2022 Jun 15;43(9):2727-2742. doi: 10.1002/hbm.25829. Epub 2022 Mar 19. Hum Brain Mapp. 2022. PMID: 35305030 Free PMC article. Review.
-
A novel missense mutation in HSF4 causes autosomal-dominant congenital lamellar cataract in a British family.Eye (Lond). 2018 Apr;32(4):806-812. doi: 10.1038/eye.2017.268. Epub 2017 Dec 15. Eye (Lond). 2018. PMID: 29243736 Free PMC article.
-
Diagnosis of Rare Diseases: a scoping review of clinical decision support systems.Orphanet J Rare Dis. 2020 Sep 24;15(1):263. doi: 10.1186/s13023-020-01536-z. Orphanet J Rare Dis. 2020. PMID: 32972444 Free PMC article.
-
Whole-genome sequencing reveals a recurrent missense mutation in the Connexin 46 (GJA3) gene causing autosomal-dominant lamellar cataract.Eye (Lond). 2018 May 1;32(10):1661-1668. doi: 10.1038/s41433-018-0154-8. Eye (Lond). 2018. PMID: 29934635 Free PMC article.
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases