Mastermind Search Companion
Extension Actions
- Live on Store
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
Latest reviews
- Matts Bell
- Allows for searching across multiple sites in parallel.
- Matts Bell
- Allows for searching across multiple sites in parallel.
- Candace Chapman
- 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.
- Mark Brown
- 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.
- Mark Brown
- 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.