Hola,
Os escribo por si a alguien le interesara participar en el panel que estamos organizando para el próximo congreso de la EASST en Madrid (6-9 julio 2022).
Panel 004 The futures of and in Genomics
Abstract:
The dramatic fall in the price and cost of genomics testing has made
possible a practice that seemed to be confined to the laboratory until a
few years ago. Testing one's DNA, or that of beings close to us is an
increasingly widespread and almost trivialised possibility. Particularly
in the reproductive sphere, where non-invasive prenatal testing,
pre-conception or gamete donor screening are emerging, but also more
simply with the use of direct-to-consumer genetic tests that can
investigate susceptibility to diseases, food intolerances, allergies,
and so on. A common element of these tests is that they use genomics to
anticipate the future in different ways: to predict the possibility of a
genetic mutation in a couple before conception, to identify the
presence of a chromosomal/genetic disorders in a foetus before it to be
born, or the predisposition to a common, multi-factorial disease before
its onset. The relationship with the future is certainly one of the
aspects that makes genomics as much promising as controversial, if not even disturbing. That
is why this panel aims to ignite a conversation around the question:
what are the futures embedded in genomics?
The possibility of a disease-free future comes along with the threat of
discriminating on the basis of DNA and, more generally, with the
imperative of knowledge-based management to optimise risk. While
healthcare systems are extremely cautious about these tests, whose
clinical usefulness they often dispute, their main driving forces are
clinics, laboratories, or private companies whose commercial strategies
rely on the symbolic power of the genome. In this space, situated on the
fringes or outside the national healthcare services or the medical
establishment, the access rules to human constitutional DNA are
reconfigured and rooted in the very materiality of the technology used.
These types of highly routinised testing practices make use of a wide
range of devices that, for instance, analyse genomes through panels of
pre-set DNA variants or segments in a quasi-automatized way. As these
panels incorporate the medical decision of what regions of DNA are worth
being analysed, they are the object of debate of international, national, or local ethics
committees, and medical associations. Also, like many other
classification systems, they tend to crystallize into standards that
compete in crafting the future of genomics. In this panel, we welcome
contributions aiming to explore how these futures embedded in genomics
reconfigure practices of consumption and subjectification, discourses
and imaginaries of health and well-being, systems of regulation of
access to DNA, and the production of testing devices. We are also open
to submissions delving into the more-than-human confines, where genetic
testing or screening are used on embryos, foetuses, or non-human animals
such as companion animals or farm animals.
Fecha límite para envíos: 1/02/2022.
Toda la información sobre el process de envío de propuestas la encontráis en
la web del congreso.
Saludos,
Violeta Argudo-Portal y Mauro Turrini