Mastermind Search Companion
The Mastermind Search Companion augments your gene and variant searches with articles citing your gene or variant from Mastermind.
Total ratings
5.00
(Rating count:
11)User reviews
Recent rating average:
5.00
All time rating average:
5.00
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| Date | Author | Rating | Lang | Comment |
|---|---|---|---|---|
| 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. What is most helpful about this extension is that it takes my searches beyond typical lit review in Google Scholar by compiling/standardizing results from multiple sites (like ClinVar, HGMD, and COSMIC). It saves me a lot of time, and I have confidence in the quality of results. | |
| 2022-05-18 |  | | Allows for searching across multiple sites in parallel. | |
| 2022-05-18 |  | | en | Allows for searching across multiple sites in parallel. |
| 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. | |
| 2022-05-18 |  | | en | 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. |
| 2022-05-18 |  | | This tool is a time saver. Very easy to use. Definitely would recommend to make any database search easier. | |
| 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. | |
| 2018-03-31 |  | | en | 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. |