Contributors -- Introduction -- Section One: Balancing Individual and Collective Interests -- "Strictly Biomedical? Sketching the Ethics of the Big Data Ecosystem in Biomedicine"; Effy Vayena and Urs Gasser -- Using Transactional Big Data for Epidemiological Surveillance: Google Flu Trends and Ethical Implications of 'Infodemiology'; Annika Richterich -- Denmark at a Crossroad? Intensified Data Sourcing in a Research Radical Country; Klaus Hoeyer -- A Critical Examination of Policy-Developments in Information Governance and the Biosciences; Edward Hockings -- Section Two: Privacy and Data Protection -- Many Have it Wrong - Samples Do Contain Personal Data: The Data Protection Regulation as a Superior Framework to Protect Donor Interests in Biobanking and Genomic Research; Dara Hallinan and Paul De Hert -- What's Wrong With the Right to Genetic Privacy: Beyond Exceptionalism, Parochialism and Adventitious Ethics; Bryce Goodman -- Section Three: Consent -- How Data are Transforming the Landscape of Biomedical Ethics: The Need for Elsi Metadata on Consent; J. Patrick Woolley -- On the Compatibility of Big Data Driven Research and Informed Consent - The Example of the Human Brain Project; Markus Christen, Josep Domingo-Ferrer, Bogdan Draganski, Tade Spranger, Henrik Walter -- Section Four: Ethical Governance -- Big Data Governance: Solidarity and the Patient Voice; Simon Woods -- Premises for Clinical Genetics Data Governance: Grappling With Diverse Value Logics; Polyxeni Vassilakopoulou, Espen Skorve, Margunn Aanestad -- State Responsibility and Accountability in Managing Big Data in Biobank Research - Tensions and Challenges in the Right of Access to Data; Aaro Tupasela and Sandra Liede -- Big Data, Small Talk: Lessons From the Ethical Practices of Interpersonal Communication for the Management of Biomedical Big Data; Paula Boddington -- Section Five: Professionalism and Ethical Duties -- Researchers' Duty to Share Pre-Publication Data: From the Prima Facie Duty to Practice; Christoph Schickhardt, Nelson Hosley, Eva C. Winkler -- Reporting and Transparency in Big Data: The Nexus of Ethics and Methodology; Stuart G Nicholls, Sinéad M. Langan, Eric I. Benchimol -- Creating a Culture of Ethics in Biomedical Big Data: Adapting 'Guidelines for Professional Practice' to Promote Ethical Use and Research Practice; Rochelle E. Tractenberg -- Section Six: Foresight -- The Ethics and Politics of Infrastructures: Creating the Conditions of Possibility for Big Data in Medicine; Linda F. Hogle -- Ethical Reuse of Data From Health Care: Data, Persons and Interests; Pete Mills -- The Ethics of Big Data: Current and Foreseeable Issues in Biomedical Contexts; Brent Daniel Mittelstadt and Luciano Floridi.