PheWeb statistics

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Citations per year

Number of citations per year for the bioinformatics software tool PheWeb
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Tool usage distribution map

This map represents all the scientific publications referring to PheWeb per scientific context
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Associated diseases

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Popular tool citations

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PheWeb specifications

Information


Unique identifier OMICS_16276
Name PheWeb
Interface Web user interface
Restrictions to use None
Biological technology Illumina
Programming languages Python
Computer skills Basic
Stability Stable
Maintained Yes

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Maintainer


  • person_outline Peter VandeHaar

Information


Unique identifier OMICS_16276
Name PheWeb
Software type Package/Module
Interface Command line interface
Restrictions to use None
Operating system Unix/Linux
Programming languages Python
License MIT License
Computer skills Advanced
Stability Stable
Requirements
Flask, pysam, marisa-trie, flask-compress, intervaltree, tqdm, openpyxl, scipy, numpy, attrdict, requests, gunicorn, boltons, blist
Maintained Yes

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Versioning


No version available

Maintainer


  • person_outline Peter VandeHaar

PheWeb citation

library_books

Evaluation of Gene Based Family Based Methods to Detect Novel Genes Associated With Familial Late Onset Alzheimer Disease

2018
Front Neurosci
PMCID: 5893779
PMID: 29670507
DOI: 10.3389/fnins.2018.00209

[…] le sclerosis (Baranzini et al., ). Missense and frameshift variants in CPAMD8 were identified in three families affected with Anterior Segment Dysgenesis (Cheong et al., ). According to the UKBiobank PheWeb (http://pheweb.sph.umich.edu:5000/), CPAMD8 has a 2.9 × 10−9 p-value for its association with AD. We did not find any shared pathway between CPAMD8 and known AD genes in the GeneMANIA network, […]


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PheWeb institution(s)
Computational Medicine and Bioinformatics, U-M Medical School, University of Michigan, MI, USA

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