The Mastermind Search Companion augments your gene and variant searches with articles citing your gene or variant from Mastermind.

Latest Version

Version
2.0
Update
January 13, 2022
Size
2.36MiB
Developer
genomenon.com
Category
Users
2,000+
Rating
5 ★
Manifest Version
3
Web Store Status
Languages Support
English
See more
Permissions
Storage
Tabs
See more

Mastermind Search Companion Extension

Mastermind Search Companion is used with the Mastermind Genomic Search Engine to optimize genomic variant research and interpretation by seamlessly integrating with the sites you already use. With Search Companion, you can:

Easily view helpful gene and variant information in the new sliding drawer tab with links to the evidence in Mastermind

Speed up your existing workflow without having to change it with the integrated display of Mastermind data in a variety of platforms you already use

Find more articles for your search when using ClinVar, HGMD, dbSNP, old dbSNP, OMIM, COSMIC, CIViC, UCSC Browser, Google Scholar, Google, VarSome, GeneCards, NCBI, Gnomad, SNPedia, and OncoKB by tapping into Mastermind data

Quickly compare Mastermind search results with results from the other platforms

For more information about Mastermind, visit the Mastermind Genomic Search Engine page: https://www.genomenon.com/mastermind/

Platforms

ClinVar

HGMD

dbSNP (new)

dbSNP (old)

OMIM

COSMIC

CIViC

UCSC Browser

Google Scholar

Google

VarSome

GeneCards

NCBI

Gnomad

SNPedia

OncoKB
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Source Manifest.json

{"update_url": "https://clients2.google.com/service/update2/crx", "name": "Mastermind Search Companion", "short_name": "Mastermind", "version": "2.0", "manifest_version": 3, "description": "The Mastermind Search Companion augments your gene and variant searches with articles citing your gene or variant from Mastermind.", "icons": { "16": "mm16.png", "48": "mm48.png", "128": "mm128.png" }, "content_scripts": [ { "matches": ["*://*/*"], "run_at": "document_idle", "js": ["content_scripts.js", "drawer.js"], "all_frames": true } ], "background": { "service_worker": "service_worker.js" }, "action": { "default_icon": "mm48.png" }, "options_ui": { "page": "options.html" }, "permissions": ["storage", "tabs"], "host_permissions": ["http://*/", "https://*/"], "web_accessible_resources": [ { "resources": ["*.png", "*.svg"], "matches": [""] } ], "key": "MIIBIjANBgkqhkiG9w0BAQEFAAOCAQ8AMIIBCgKCAQEAusvtTFZfFFcuVrCj/epmymIYjwILPmznc2e40UkcS6Ghn55tgVdQy/01pD9OmbgvQQt/LRnbvXDD65TDkpKr0bXSXraA8JV030IlQj/u/J7w8vCkxIsIyeKh04cnihyUNUll39nYsp7ikjKUMJiMT8uYUqcj8ptVUgpOVjgVJLKbat4+r18Q0mk4WN8p9f3guNuNB7dihtUTc3WGJ9AKwgHUb0eKRgvEo1Xxg5ptGnCw+D+IHVuX+WCm+WA2bJNQig8JWoipYmnpdiS+jPdwc81qlDSD7EWQdUWWSO+F9ZNdQI7hjYVJsl9stic0X5511enB1yOi4qWEH4XFFYstgwIDAQAB"}
Read more

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User reviews

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Matts Bell (ID: 000000f2873df2b3) Voted 5 ★ - Updated 05/18/2022 Allows for searching across multiple sites in parallel.

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Mark Brown (ID: 000000b78da41949) Voted 5 ★ - Updated 05/18/2022 Very useful tool that overlays on ClinVar, HGMD, dbSNP, OMIM, COSMIC, CIViC, UCSC Browser, Google Scholar, VarSome, GeneCards, NCBI, Gnomad, SNPedia, & OncoKB. Quickly shows number of articles in PubMed containing the variant (no matter how the author describes it), A view of the variants published across the protein, transcripts, amino acid & CDNA positions & genomic positions.