Få besked, når der er ændringer til dette udbud Gem dette udbud under "Mine udbud"

Databasesystemer 2021/S 142-377891

Kort beskrivelse

The solution will be used by clinical scientists from the regional healthcare system as well as researchers from the universities. They will log into the NCG HPC system and access the solution preferably through third party interpretation software, or directly via an internet browser. With the genetic variant database software/tool they should be able to filter variants based on several criteria, e.g. mutation type, pathogenicity score, disease, location in gene/genome etc. This section clarifies that any standard terms that are in conflict with the described use of licenses are set a side.

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Ordregiver Nationalt Genom Center
Annonceret 26-07-2021 kl. 00.00
Sidst ændret 26-07-2021 kl. 10.00
Deadline 20-08-2021 Se klokkeslæt under udbudsdetaljer
Udbudstype EU-udbud
Udbudsdetaljer https://ted.europa.eu/udl?uri=TED:NOTICE:377891-2021:TEXT:EN:HTML
Leveringssted DANMARK
Dokumenttype Bekendtgørelse om ændringer eller supplerende oplysninger

Bekendtgørelse om ændringer eller supplerende oplysninger (21-07-2021)

Databasesystemer 2021/S 139-369878

https://ted.europa.eu/udl?uri=TED:NOTICE:369878-2021:TEXT:EN:HTML
Kort beskrivelse

The solution will be used by clinical scientists from the regional healthcare system as well as researchers from the universities. They will log into the NCG HPC system and access the solution preferably through third party interpretation software, or directly via an internet browser. With the genetic variant database software/tool they should be able to filter variants based on several criteria, e.g. mutation type, pathogenicity score, disease, location in gene/genome, etc. This section clarifies that any standard terms that are in conflict with the described use of licenses are set a side.

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Ordregiver Nationalt Genom Center
Annonceret 21-07-2021 kl. 00.00
Sidst ændret 21-07-2021 kl. 10.00
Deadline 06-08-2021 Se klokkeslæt under udbudsdetaljer
Udbudstype EU-udbud
Udbudsdetaljer https://ted.europa.eu/udl?uri=TED:NOTICE:369878-2021:TEXT:EN:HTML
Leveringssted DANMARK
Dokumenttype Bekendtgørelse om ændringer eller supplerende oplysninger

Udbudsbekendtgørelse (12-07-2021)

Databasesystemer 2021/S 132-350096

https://ted.europa.eu/udl?uri=TED:NOTICE:350096-2021:TEXT:EN:HTML
Kort beskrivelse

The solution will be used by clinical scientists from the regional healthcare system as well as researchers from the universities. They will log into the NCG HPC system and access the solution preferably through third party interpretation software, or directly via an internet browser. With the genetic variant database software/tool they should be able to filter variants based on several criteria, e.g. mutation type, pathogenicity score, disease, location in gene/genome etc. This section clarifies that any standard terms that are in conflict with the described use of licenses are set a side.

Læs mere
Ordregiver Nationalt Genom Center
Annonceret 12-07-2021 kl. 00.00
Sidst ændret 12-07-2021 kl. 10.00
Deadline 04-08-2021 Se klokkeslæt under udbudsdetaljer
Udbudstype EU-udbud
Udbudsdetaljer https://ted.europa.eu/udl?uri=TED:NOTICE:350096-2021:TEXT:EN:HTML
Leveringssted DANMARK
Dokumenttype Udbudsbekendtgørelse