Mastermind Search Companion
Overview
Mastermind Search Companion is a Chrome extension developed by Genomenon Inc..
According to the data from Chrome web store, current version of Mastermind Search Companion is 2.0, updated on 2022-01-13.
2,000+ users have installed this extension.
13 users have rated this extension with an average rating of .
developer website: genomenon.com
The Mastermind Search Companion augments your gene and variant searches with articles citing your gene or variant from Mastermind.
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
VarSome
GeneCards
NCBI
Gnomad
SNPedia
OncoKB
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Latest Reviews
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Garrett Sheets
2022-05-19
A big part of my work is collecting and organizing information from a variety of genomic resources, and ensuring that it is complete, accurate, and up-to-date. |
Matts Bell
2022-05-18
Allows for searching across multiple sites in parallel. |
Candace Chapman
2022-05-18
This is an excellent tool for finding genomic literature regardless of nomenclature. It reaches into all the sites I would use and finds more evidence than any of them. |
Jake Kastroll
2022-05-18
This tool is a time saver. Very easy to use. Definitely would recommend to make any database search easier. |
Mark Brown
2022-05-18
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. |