3,267 research outputs found

    Genomics and Privacy: Implications of the New Reality of Closed Data for the Field

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    Open source and open data have been driving forces in bioinformatics in the past. However, privacy concerns may soon change the landscape, limiting future access to important data sets, including personal genomics data. Here we survey this situation in some detail, describing, in particular, how the large scale of the data from personal genomic sequencing makes it especially hard to share data, exacerbating the privacy problem. We also go over various aspects of genomic privacy: first, there is basic identifiability of subjects having their genome sequenced. However, even for individuals who have consented to be identified, there is the prospect of very detailed future characterization of their genotype, which, unanticipated at the time of their consent, may be more personal and invasive than the release of their medical records. We go over various computational strategies for dealing with the issue of genomic privacy. One can “slice” and reformat datasets to allow them to be partially shared while securing the most private variants. This is particularly applicable to functional genomics information, which can be largely processed without variant information. For handling the most private data there are a number of legal and technological approaches—for example, modifying the informed consent procedure to acknowledge that privacy cannot be guaranteed, and/or employing a secure cloud computing environment. Cloud computing in particular may allow access to the data in a more controlled fashion than the current practice of downloading and computing on large datasets. Furthermore, it may be particularly advantageous for small labs, given that the burden of many privacy issues falls disproportionately on them in comparison to large corporations and genome centers. Finally, we discuss how education of future genetics researchers will be important, with curriculums emphasizing privacy and data security. However, teaching personal genomics with identifiable subjects in the university setting will, in turn, create additional privacy issues and social conundrums

    Tapping the Potential of Traditional Knowledge Associated with Medicinal Plants of Tribal Communities in Central India: Perspective and Avenues

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    India is known to have over 700 scheduled tribes which are native to five different regions viz., Himalayan, Central, Western, Dravidian and islands, each having its own primitive trait and cultural distinction. Out of these diverse territories, Central Indian region has the distinction of hosting 55% of the total tribal population of India which provides diverse region for bioprospecting. This region provides a natural, invaluable store house of indigenous medicinal plant diversity that is of great importance for mankind. Protection of traditional knowledge of these tribal communities residing in central India is the need of hour as overexploitation of natural resources due to increase in population may lead to extinction of important medicinal plant species. With careful management of the natural resources a sustainable balance can be achieved. The review envisages providing baseline data on important tribal communities and their status, traditional knowledge, medicinal properties of native plants of tribals and gives an insight for exploitation of these plants by pharmaceutical industry as well as insilico approach for screening new active compounds and drug designing

    Controlling new knowledge: Genomic science, governance and the politics of bioinformatics

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    The rise of bioinformatics is a direct response to the political difficulties faced by genomics in its quest to be a new biomedical innovation, its value being that it acts as the bridge between the promise of genomics and its realization in the form of health benefits. Western scientific elites are able to use their close relationship with the state to control and facilitate the emergence of new domains compatible with the existing distribution of epistemic power – all within the embrace of public trust. The incorporation of bioinformatics as the saviour of genomics had to be integrated with the operation of two key aspects of governance in this field: the definition and ownership of the new knowledge. This was achieved mainly by the development of common standards and by the promotion of the values of communality, open access and the public ownership of data to legitimize and maintain the governance power of publicly funded genomic science. Opposition from industry advocating the private ownership of knowledge has been largely neutered through the institutions supporting the science-state concordat. However, in order for translation into health benefit to occur and public trust to be assured, genomic and clinical data have to be integrated and knowledge ownership agreed across the separate and distinct governance territories of scientist, clinical medicine and society. Tensions abound as science seeks ways of maintaining its control of knowledge production through the negotiation of new forms of governance with the institutions and values of clinicians and patients
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