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Part 2 focuses on some specific challenges that that arise for the traditional informed-consent process in population-wide genetics\/genomics research, especially where data-mining techniques are used. In the third and final section, we defend a model of consent based on the notion of a \"charitable trust,\" which we believe can help to preserve the integrity of the consent process in the context of medical and genetic research involving DNA databanks.<\/jats:p>","DOI":"10.1145\/1839994.1839996","type":"journal-article","created":{"date-parts":[[2010,8,11]],"date-time":"2010-08-11T12:57:24Z","timestamp":1281531444000},"page":"11-21","update-policy":"https:\/\/doi.org\/10.1145\/crossmark-policy","source":"Crossref","is-referenced-by-count":2,"title":["The consent process in medical research involving DNA databanks"],"prefix":"10.1145","volume":"40","author":[{"given":"Herman T.","family":"Tavani","sequence":"first","affiliation":[{"name":"Rivier College"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Maria","family":"Bottis","sequence":"additional","affiliation":[{"name":"Ionian University (Greece)"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"320","published-online":{"date-parts":[[2010,6]]},"reference":[{"volume-title":"Goodman, K.E. 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