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Active HORIZON European Commission

Using museum specimens to understand mushroom population genomics.


Funder European Commission
Recipient Organization Universitetet I Oslo
Country Norway
Start Date Feb 01, 2024
End Date Jan 31, 2026
Duration 730 days
Number of Grantees 2
Roles Associated Partner; Coordinator
Data Source European Commission
Grant ID 101103900
Grant Description

Museum collections and other repositories contain a vast amount of specimens associated with metadata detailing the location,habitat and ecological observations of the specimen at the moment of collection. Since these specimens are biological tissues, DNAsequencing techniques can be used to study them.

However, their application to fungi is still very limited.

One of such applications ispopulation genomics, a field where fungal study is also severely lagging behind that of plants and animals.

The combination ofsequences from museum specimens and fresh material will allow us to study populations of two mushroom-forming fungi,Trichaptum abietinum and Phelopillus nigrolimitatus.

T. abietinum is an abundant species that is emerging as a model for population studies, with abundant information in Scandinavia.

Museum samples will allow us to detect potential changes in selective forces that have affected Norwegian populations, mainly associated with landscape changes over the XXth century.

P. nigrolimitatus is a Scandinavian Nearly Threatened species whose populations have been dwindling in association to land usechanges.

Museum samples will allow us to compare past and current genetic diversity of Norwegian populations, which will helpinform conservation efforts.

The project will generate SNP chips, which will help future population and conservation studies by providing a reliable and cost-efficient analytical tool.

MUSHEUM will combine population genomic data with specimen metadata and ecological information to study selective pressures in the two species.

Finally, MUSHEUM will make use of the combined genome skimming data generated for the design of SNP probes to generate de novo genome assemblies of the two species. This advances will allow to repurpose data from population studies for the generation of reference assemblies.

All Grantees

Biofokus; Universitetet I Oslo

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