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CoDisEASe SIGNED

Communicable Disease in the Age of Seafaring

Total Cost €

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EC-Contrib. €

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Partnership

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 CoDisEASe project word cloud

Explore the words cloud of the CoDisEASe project. It provides you a very rough idea of what is the project "CoDisEASe" about.

dynamic    regular    date    permit    easily    changing    formed    world    history    interrogated    genomic    permitted    local    immunity    evaluations    ancient    directions    emergence    landscapes    movement    peoples    diseases    colonisation    underexplored    host    selective    pathogenic    continents    geographical    sensitive    subject    shaped    humans    molecular    identities    roles    trade    epidemics    unification    rest    source    pressures    contact    temporal    interactions    genetic    collided    intimate    series    vast    had    barriers    interchange    relative    african    human    scholarly    territory    played    genes    pathogen    transfers    cultures    millennia    dna    introductions    historical    navigation    global    discovery    biological    skeletal    century    disease    north    interconnected    worlds    interrelationships    complementary    communities    american    autonomy    makeup    though    details    resolution    morphology    data    eurasian    unprecedented    post    clear    infectious    exchange    permitting    quantitative    plentiful    insults    europeans    improvements    evaluation    ecological    generating    period    acquired    americas    light    presented    travel    terminal    genomes    limited    pleistocene    loci    documents    fifteenth   

Project "CoDisEASe" data sheet

The following table provides information about the project.

Coordinator
MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV 

Organization address
address: HOFGARTENSTRASSE 8
city: MUENCHEN
postcode: 80539
website: n.a.

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Germany [DE]
 Total cost 1˙490˙043 €
 EC max contribution 1˙490˙043 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-STG
 Funding Scheme ERC-STG
 Starting year 2018
 Duration (year-month-day) from 2018-12-01   to  2023-11-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV DE (MUENCHEN) coordinator 1˙490˙043.00

Map

Leaflet | Map data © OpenStreetMap contributors, CC-BY-SA, Imagery © Mapbox

 Project objective

Infectious diseases have had an intimate history with humans and have shaped our genetic makeup through generating strong selective pressures. Although disease emergence and epidemics occur on a local scale, human interrelationships formed through travel and trade can lead to exchanges of pathogenic communities. While such transfers were common among the interconnected Eurasian and North African cultures throughout most of human history, the rest of the world experienced relative ecological autonomy. The terminal Pleistocene witnessed the colonisation of vast territory on the American continents, after which interactions between New and Old World peoples were limited for millennia by geographical barriers. These ecological worlds collided at the end of the fifteenth century, when improvements in navigation and the discovery of the Americas by Europeans permitted regular contact and plentiful opportunities for biological interchange. The identities of most diseases that played leading roles during this period of exchange are known, though details on the directions of their movement and temporal introductions remain the subject of scholarly debate. The work programme presented here will use an underexplored data source – ancient pathogen genomes – to identify infectious insults in pre- and post-contact New and Old World skeletal series, thus enabling an evaluation of changing disease landscapes at contact. Complementary to this goal, genomic loci for human immunity genes will be interrogated, thus permitting quantitative evaluations of disease adaptation. Ancient molecular data will be acquired through use of the most sensitive and up to date methods in the field of ancient DNA with the aim of bringing diseases not easily seen from skeletal morphology or historical documents to light in clear detail. This will permit an unprecedented resolution of past disease experience and host-pathogen interactions during this dynamic period of global ecological unification.

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The information about "CODISEASE" are provided by the European Opendata Portal: CORDIS opendata.

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