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TABLE OF CONTENTS
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August 2012 Volume 9, Issue 8 |
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Editorial
This Month
Correspondence
Research Highlights
Methods in Brief
Tools in Brief
Technology Feature
News and Views
Analysis
Brief Communications
Articles
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In This Issue | Top |
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In This Issue
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Editorial | Top |
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In praise of referees p765 doi:10.1038/nmeth.2136 Peer review is an essential part of scientific discourse, and referees deserve formal recognition for the service they provide.
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This Month | Top |
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The author file: Gustavo Stolovitzky p767 Monya Baker doi:10.1038/nmeth.2113 Boosting accuracy by building consensus.
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Points of view: Mapping quantitative data to color p769 Nils Gehlenborg and Bang Wong doi:10.1038/nmeth.2134 Data structure informs choice of color maps.
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Correspondence | Top |
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Reanalysis of phosphoproteomics data uncovers ADP-ribosylation sites pp771 - 772 Ivan Matic, Ivan Ahel and Ronald T Hay doi:10.1038/nmeth.2106
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jModelTest 2: more models, new heuristics and parallel computing p772 Diego Darriba, Guillermo L Taboada, Ramón Doallo and David Posada doi:10.1038/nmeth.2109
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CircadiOmics: integrating circadian genomics, transcriptomics, proteomics and metabolomics pp772 - 773 Vishal R Patel, Kristin Eckel-Mahan, Paolo Sassone-Corsi and Pierre Baldi doi:10.1038/nmeth.2111
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OpenFovea: open-source AFM data processing software pp774 - 775 Charles Roduit, Bhaskar Saha, Livan Alonso-Sarduy, Andrea Volterra, Giovanni Dietler and Sandor Kasas doi:10.1038/nmeth.2112
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Research Highlights | Top |
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Methods in Brief | Top |
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The ins and outs of optogenetic silencers | Quantifying single transcripts | Toward deep-tissue fluorescence imaging | Neural progenitors from fibroblasts
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Tools in Brief | Top |
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RNA and the proteins that bind | Synaptic activity shines in red | Shutting down parts of the glycome | Long noncoding RNAs in the worm
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Technology Feature | Top |
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RNA imaging in situ pp787 - 790 Monya Baker doi:10.1038/nmeth.2108 Rapidly maturing techniques reveal messengers within cells.
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News and Views | Top |
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High-speed microbial community profiling pp793 - 794 Daniel H Haft and Andrey Tovchigrechko doi:10.1038/nmeth.2080 A precomputed database of lineage-restricted reference genes yields a fast and accurate tool that uses sequence similarity alone to compute clade abundances from shotgun metagenomic data sets.
See also: Brief Communication by Segata et al.
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Connecting ecology and conservation through experiment pp794 - 795 Nick M Haddad doi:10.1038/nmeth.2107 An experimental infrastructure consisting of environmentally controlled and spatially linked habitat patches permits studies on terrestrial animal dispersal at an unprecedented scale for an experiment with such strict control.
See also: Article by Legrand et al.
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Analysis | Top |
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Wisdom of crowds for robust gene network inference pp796 - 804 Daniel Marbach, James C Costello, Robert Küffner, Nicole M Vega, Robert J Prill, Diogo M Camacho, Kyle R Allison, The DREAM5 Consortium, Manolis Kellis, James J Collins and Gustavo Stolovitzky doi:10.1038/nmeth.2016 This analysis comprehensively compares methods for gene regulatory network inference submitted through the DREAM5 challenge. It demonstrates that integration of predictions from multiple methods shows the most robust performance across data sets.
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Brief Communications | Top |
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Targeted gene knockout by direct delivery of zinc-finger nuclease proteins pp805 - 807 Thomas Gaj, Jing Guo, Yoshio Kato, Shannon J Sirk and Carlos F Barbas III doi:10.1038/nmeth.2030 Due to an unexpected cell-penetrating property, zinc-finger nucleases (ZFNs) can be delivered to several mammalian cell types as proteins. Dose-dependent disruption of an endogenous gene was achieved with reduced activity at known off-target sites.
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2b-RAD: a simple and flexible method for genome-wide genotyping pp808 - 810 Shi Wang, Eli Meyer, John K McKay and Mikhail V Matz doi:10.1038/nmeth.2023 Genotyping based on restriction site7ndash;associated (RAD) sequencing around type IIB enzyme recognition sites is reported. The streamlined reduced-representation approach features even and tunable genome coverage and enables large-scale genotyping studies by maximizing the amount of genotypic information that can be obtained from individuals for a given amount of sequencing.
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Metagenomic microbial community profiling using unique clade-specific marker genes pp811 - 814 Nicola Segata, Levi Waldron, Annalisa Ballarini, Vagheesh Narasimhan, Olivier Jousson and Curtis Huttenhower doi:10.1038/nmeth.2066 MetaPhlAn (metagenomic phylogenetic analysis) allows the rapid and accurate identification of microbial species and higher clades from shotgun sequencing data.
See also: News and Views by Haft & Tovchigrechko
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Multicolor two-photon tissue imaging by wavelength mixing pp815 - 818 Pierre Mahou, Maxwell Zimmerley, Karine Loulier, Katherine S Matho, Guillaume Labroille, Xavier Morin, Willy Supatto, Jean Livet, Delphine Débarre and Emmanuel Beaurepaire doi:10.1038/nmeth.2098 This method achieves simultaneous and spatially colocalized excitation of three fluorophores with distinct spectra, doing so via two-photon microscopy using a femtosecond laser and an optical parametric oscillator and by temporally overlapping the beams. Imaging of 'Brainbow'-labeled mouse and chicken nervous tissue and of developing fly embryos is shown.
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forestSV: structural variant discovery through statistical learning pp819 - 821 Jacob J Michaelson and Jonathan Sebat doi:10.1038/nmeth.2085 A machine learning-based structural-variant discovery approach that incorporates prior knowledge shows high sensitivity and specificity even on single genomes.
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A protease for 'middle-down' proteomics pp822 - 824 Cong Wu, John C Tran, Leonid Zamdborg, Kenneth R Durbin, Mingxi Li, Dorothy R Ahlf, Bryan P Early, Paul M Thomas, Jonathan V Sweedler and Neil L Kelleher doi:10.1038/nmeth.2074 A rare cutting protease that creates large peptides is well suited for differentiating protein isoforms and detecting combinations of post-translational modifications by tandem mass spectrometry.
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Scanning angle interference microscopy reveals cell dynamics at the nanoscale pp825 - 827 Matthew J Paszek, Christopher C DuFort, Matthew G Rubashkin, Michael W Davidson, Kurt S Thorn, Jan T Liphardt and Valerie M Weaver doi:10.1038/nmeth.2077 This paper reports a fluorescence imaging method based on interference contrast in which the incidence angle of the excitation light is actively scanned. The high axial precision and temporal resolution are used for dynamic nanoscale imaging of cytoskeleton and adhesion proteins in living cells.
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Articles | Top |
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The Metatron: an experimental system to study dispersal and metaecosystems for terrestrial organisms pp828 - 833 Delphine Legrand, Olivier Guillaume, Michel Baguette, Julien Cote, Audrey Trochet, Olivier Calvez, Susanne Zajitschek, Felix Zajitschek, Jane Lecomte, Quentin Bénard, Jean-François Le Galliard and Jean Clobert doi:10.1038/nmeth.2104 A flexible, environmentally controlled experimental setup for the study of terrestrial animal dispersal is reported. Its unprecedented scale should enable studies in spatial ecology and permit tests of conservation strategies in the face of environmental change.
See also: News and Views by Haddad
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Facile backbone structure determination of human membrane proteins by NMR spectroscopy pp834 - 839 Christian Klammt, Innokentiy Maslennikov, Monika Bayrhuber, Cédric Eichmann, Navratna Vajpai, Ellis Jeremy Chua Chiu, Katherine Y Blain, Luis Esquivies, June Hyun Jung Kwon, Bartosz Balana, Ursula Pieper, Andrej Sali, Paul A Slesinger, Witek Kwiatkowski, Roland Riek and Senyon Choe doi:10.1038/nmeth.2033 The combination of cell-free protein expression and combinatorial dual labeling-aided NMR analysis allows for the rapid backbone structure assessment of human membrane proteins.
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High-throughput assessment of microRNA activity and function using microRNA sensor and decoy libraries pp840 - 846 Gavriel Mullokandov, Alessia Baccarini, Albert Ruzo, Anitha D Jayaprakash, Navpreet Tung, Benjamin Israelow, Matthew J Evans, Ravi Sachidanandam and Brian D Brown doi:10.1038/nmeth.2078 Two large-scale resources for studying microRNA function are presented: one is a library of fluorescent sensors with a corresponding assay for global profiling of microRNA activity in different cell types; the other is a decoy library for suppressing microRNA activity individually or in pooled loss-of-function screens.
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Nature Chemical Biology Focus on Metabolism in 3D
In this focus issue, we feature a collection of commentary and review articles that outline some of the ideas, advances and goals that are laying the foundations for the next era of metabolism research.
To access the Focus, visit: www.nature.com/nchembio/focus/metabolism3d/index.html |
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