American Journal of Human Biology : Leading Innovation in Human Population Biology Research

2019 ◽  
Vol 31 (5) ◽  
Author(s):  
William R. Leonard
2017 ◽  
Vol 1 (3) ◽  
pp. 245-248 ◽  
Author(s):  
Chris P. Ponting

With so much genomics data being produced, it might be wise to pause and consider what purpose this data can or should serve. Some improve annotations, others predict molecular interactions, but few add directly to existing knowledge. This is because sequence annotations do not always implicate function, and molecular interactions are often irrelevant to a cell's or organism's survival or propagation. Merely correlative relationships found in big data fail to provide answers to the Why questions of human biology. Instead, those answers are expected from methods that causally link DNA changes to downstream effects without being confounded by reverse causation. These approaches require the controlled measurement of the consequences of DNA variants, for example, either those introduced in single cells using CRISPR/Cas9 genome editing or that are already present across the human population. Inferred causal relationships between genetic variation and cellular phenotypes or disease show promise to rapidly grow and underpin our knowledge base.


2012 ◽  
Vol 53 (S5) ◽  
pp. S222-S232 ◽  
Author(s):  
Trudy R. Turner

2014 ◽  
Vol 27 (1) ◽  
pp. 6-15 ◽  
Author(s):  
Julia Ravenscroft ◽  
Lawrence M. Schell ◽  
Tewentahawih′tha′ Cole

Man ◽  
1990 ◽  
Vol 25 (4) ◽  
pp. 715
Author(s):  
C. G. N. Mascie-Taylor ◽  
Michael A. Little ◽  
Jere D. Haas

Author(s):  
Theresa E. Gildner ◽  
Geeta N. Eick ◽  
Alaina L. Schneider ◽  
Felicia C. Madimenos ◽  
J. Josh Snodgrass

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