The outstanding scientist, R.A. Fisher:His views on eugenics and race

R.A. Fisher was one of the greatest scientists of the 20th century (Fig. 1). He was a man of extraordinary ability and originality whose scientific contributions ranged over a very wide area of science, from biology through statistics to ideas on continental drift, and whose work has had a huge positive impact on human welfare. Not surprisingly, some of his large volume of work is not widely used or accepted at the current time, but his scientific brilliance has never been challenged. He was from an early age a supporter of certain eugenic ideas, and it is for this reason that he has been accused of being a racist and an advocate of forced sterilisation (Evans 2020). His promotion of eugenics has recently caused various organisations to remove his name from awards and dedications of buildings (Tarran 2020; Rothamsted Research 2020; Society for the Study of Evolution 2020; Gonville and Caius College 2020). A primary aim of this paper is to conduct a careful analysis of his own writings in these areas. Our purpose is neither to defend nor attack Fisher’s work in eugenics and views on race, but to present a careful account of their substance and nature.Publisher PDFPeer reviewe

LMDA Newsletter, July 1, 2016

Contents include: Letter from the Editor; A Message from our LMDA President; Canadian Fellows: Vicki Stroich & Bob White in Conversation; Freelancing Across America: On the Road with Heather Helinsky; From Producing to Freelancing: Artistic Leaders Jayne Wenger & Mead Hunter; Freelancing in Canada: David Geary Talks Shop & Indigenous Dramaturgy; Early Career Projects: Anna Woodruff Collaborates with Melis Aker; Benches We Have Shared: Elizabeth Bennett & Liz Engelman Talk Life after Institutional Dramaturgy; Upcoming Events.https://soundideas.pugetsound.edu/lmdanewsletter/1008/thumbnail.jp

An interactive genome browser of association results from the UK10K cohorts project.

UNLABELLED: High-throughput sequencing technologies survey genetic variation at genome scale and are increasingly used to study the contribution of rare and low-frequency genetic variants to human traits. As part of the Cohorts arm of the UK10K project, genetic variants called from low-read depth (average 7×) whole genome sequencing of 3621 cohort individuals were analysed for statistical associations with 64 different phenotypic traits of biomedical importance. Here, we describe a novel genome browser based on the Biodalliance platform developed to provide interactive access to the association results of the project. AVAILABILITY AND IMPLEMENTATION: The browser is available at http://www.uk10k.org/dalliance.html. Source code for the Biodalliance platform is available under a BSD license from http://github.com/dasmoth/dalliance, and for the LD-display plugin and backend from http://github.com/dasmoth/ldserv