Friday, September 15, 2017

Nature Reviews Genetics Contents October 2017 Volume 18 Number 10 pp 577-636

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Nature Reviews Genetics
 

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TABLE OF CONTENTS
 
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Nature Reviews Genetics cover
2016 2-year Impact Factor 40.282 Journal Metrics 2-year Median 28.5
In this issue
Research Highlights
Reviews
 
Also this month
 Featured article:
Settling the score: variant prioritization and Mendelian disease
Karen Eilbeck, Aaron Quinlan & Mark Yandell

 
 
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RESEARCH HIGHLIGHTS
 
Top

Model organisms: New tools, new insights — probing social behaviour in ants
p577 | doi:10.1038/nrg.2017.70
PDF


Pathogen genetics: Evolutionary dynamics driving drug resistance
p578 | doi:10.1038/nrg.2017.68
PDF


Chromosome biology: Different turfs for cohesin and condensin
p578 | doi:10.1038/nrg.2017.71
PDF


Genetic engineering: Pigs without PERVs
p579 | doi:10.1038/nrg.2017.73
PDF


Gene therapy: Human genome editing in heart disease
p580 | doi:10.1038/nrg.2017.69
PDF


 

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REVIEWS
 
Top
Evolutionary biology through the lens of budding yeast comparative genomics
Souhir Marsit, Jean-Baptiste Leducq, Éléonore Durand, Axelle Marchant, Marie Filteau & Christian R. Landry

p581 | doi:10.1038/nrg.2017.49
Saccharomyces cerevisiae has become an important model organism in the field of evolutionary genomics. Comparative genomic analysis of laboratory, wild and domesticated yeast populations is generating insights into how new species form and how populations adapt to their environments.
Abstract | Full Text | PDF

 
Settling the score: variant prioritization and Mendelian disease
Karen Eilbeck, Aaron Quinlan & Mark Yandell

p599 | doi:10.1038/nrg.2017.52
For clinical cases of Mendelian disease that lack a genetic diagnosis, genome and exome sequencing are increasingly used for seeking the genetic cause. This Review discusses the strategies and computational tools for prioritizing the many genetic variants identified in each genome into those that are most likely to be causal for disease. The authors discuss how diverse types of biochemical, evolutionary, pedigree and clinical-phenotype information are used, and they highlight common pitfalls to be aware of for responsible variant prioritization.
Abstract | Full Text | PDF

 
Synthetic lethality and cancer
Nigel J. O'Neil, Melanie L. Bailey & Philip Hieter

p613 | doi:10.1038/nrg.2017.47
The authors review the concept of synthetic lethality — when the perturbation of one of two genes alone is viable, but the perturbation of both genes simultaneously results in the loss of viability — from model organisms to human cancers, and discuss how genetic interactions can be exploited for the identification of new drug targets in cancer.
Abstract | Full Text | PDF

 
Dissecting evolution and disease using comparative vertebrate genomics
Jennifer R. S. Meadows & Kerstin Lindblad-Toh

p624 | doi:10.1038/nrg.2017.51
The last 25 years has seen a revolution in sequencing, with more than 100 vertebrate genome sequences now available. In this Review, Meadows and Lindblad-Toh discuss how the genomics of non-human organisms can provide insights into vertebrate biology and conservation, and how they can contribute to the understanding of human health and disease.
Abstract | Full Text | PDF

 
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