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Nature Reviews Genetics Contents January 2016 Volume 17 Number 1 pp 1-62

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Nature Reviews Genetics

 
TABLE OF CONTENTS
 
January 2016 Volume 17 Number 1
Nature Reviews Genetics cover
Impact Factor 36.978 *
In this issue
Comment
Research Highlights
Reviews


Also this month
Article series:
Applications of next-generation sequencing
Disease mechanisms
Non-coding RNA
 Featured article:
Unique features of long non-coding RNA biogenesis and function
Jeffrey J. Quinn & Howard Y. Chang


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Comment: Principle of proportionality in genomic data sharing
Caroline F. Wright, Matthew E. Hurles & Helen V. Firth
p1 | doi:10.1038/nrg.2015.5
Caroline Wright, Matthew Hurles and Helen Firth propose that a principle of proportionality be applied to genomic data that weighs the depth of data (what is shared) against the breadth of sharing (with whom) to find a proportionate approach that balances beneficence and non-maleficence.
Abstract | Full Text | PDF

RESEARCH HIGHLIGHTS
Top

Chromatin: Moving a TAD closer to unravelling chromosome architecture
p3 | doi:10.1038/nrg.2015.7
PDF

Disease genetics: SNP location helps predict disease aetiology
p4 | doi:10.1038/nrg.2015.12
PDF

Complex traits: A diamond in the ruff
p4 | doi:10.1038/nrg.2015.15
PDF

Gene regulation: Landscape and mechanisms of transcription factor cooperativity
p5 | doi:10.1038/nrg.2015.11
PDF

Molecular evolution: Regulatory runaways
p6 | doi:10.1038/nrg.2015.14
PDF

Techniques: Exploring protein-RNA interactions with RNA Tagging
p6 | doi:10.1038/nrg.2015.6
PDF

Molecular genetics: Through the cracked lens of cancer genomes
p7 | doi:10.1038/nrg.2015.13
PDF


IN BRIEF

Epigenomics: Sperm as obesity propagator? | Technique: Mapping open chromatin in single cells | Genetic screens: CRISPR knockout screens for human fitness genes
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Genetics
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REVIEWS
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Article series: Applications of next-generation sequencing
Genetic studies in intellectual disability and related disorders
Lisenka E. L. M. Vissers, Christian Gilissen & Joris A. Veltman
p9 | doi:10.1038/nrg3999
The phenotypic heterogeneity of intellectual disability (ID) disorders has hampered studies of the underlying genetics, but major progress has been achieved by recent applications of next-generation sequencing. This Review discusses our latest understanding of ID genetics, including the identification of de novo and inherited mutations of various types, strategies for assigning disease causality to the mutations, emerging pathological mechanisms and future research directions.
Abstract | Full Text | PDF | Supplementary information

Article series: Disease mechanisms
RNA mis-splicing in disease
Marina M. Scotti & Maurice S. Swanson
p19 | doi:10.1038/nrg.2015.3
Complex and intricate RNA splicing mechanisms are crucial for gene regulation and for maximizing proteomic diversity. This Review discusses how alterations to splicing mechanisms — such as mutations in pre-mRNAs, or mutations and dysregulation of core spliceosome proteins and other RNA-binding proteins — results in diverse molecular consequences and various diseases. Opportunities for therapeutic correction of these defects are also explored.
Abstract | Full Text | PDF

Evolution of vertebrate sex chromosomes and dosage compensation
Jennifer A. Marshall Graves
p33 | doi:10.1038/nrg.2015.2
The differentiation of sex chromosomes in vertebrates created a need for mechanisms that compensate for differences in dosage of gene expression between the sexes. The author reviews the diversity of these mechanisms, their effects on gene expression, and their origin and evolution across the major vertebrate groups.
Abstract | Full Text | PDF

Article series: Non-coding RNA
Unique features of long non-coding RNA biogenesis and function
Jeffrey J. Quinn & Howard Y. Chang
p47 | doi:10.1038/nrg.2015.10
Long non-coding RNAs (lncRNAs) are a class of RNAs with great molecular and regulatory diversity. This Review discusses how, beyond their lack of protein-coding potential, some types of lncRNAs are known to exhibit features that are distinct from mRNAs, including their transcriptional regulation, localization, processing, biological capabilities and degradation. Such properties underlie many of the key cellular functions of lncRNAs.
Abstract | Full Text | PDF

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