Thursday, August 28, 2014

Nature Methods Contents: September 2014 Volume 11 pp 875 - 972

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TABLE OF CONTENTS

September 2014 Volume 11, Issue 9

In This Issue
Editorials
This Month
Correspondence
Research Highlights
Commentaries
Technology Feature
News and Views
Brief Communications
Articles
Corrigenda
Addendum
Application Notes
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In This Issue

Top

InThisIssue   

Editorials

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The measure of reproducibility   p875
doi:10.1038/nmeth.3096
A clear idea of the performance—the strengths but also the limits—of biological research methods is critical for generating reliable data that others are able to reproduce.

Change at Nature Methods   p875
doi:10.1038/nmeth.3097
We announce a change in leadership at Nature Methods and wish Daniel Evanko, our departing chief editor and the new head of editorial services at Nature Publishing Group, every success.

This Month

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The Author File: Richard Neutze   p877
Vivien Marx
doi:10.1038/nmeth.3074
Proteins 'breathe' in an ultrafast way that can be captured with XFELs.

Points of Significance: Replication   pp879 - 880
Paul Blainey, Martin Krzywinski and Naomi Altman
doi:10.1038/nmeth.3091
Quality is often more important than quantity.

Correspondence

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Light-sheet functional imaging in fictively behaving zebrafish   pp883 - 884
Nikita Vladimirov, Yu Mu, Takashi Kawashima, Davis V Bennett, Chao-Tsung Yang et al.
doi:10.1038/nmeth.3040

See also: News and Views by Cunningham

Guided visual exploration of genomic stratifications in cancer   pp884 - 885
Marc Streit, Alexander Lex, Samuel Gratzl, Christian Partl, Dieter Schmalstieg et al.
doi:10.1038/nmeth.3088

Research Highlights

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Nanopores read long genomic DNA
An ion-current map characteristic of four nucleotides traversing a protein nanopore allows resequencing of long DNA reads.

Optical inhibition in red
The red light-sensitive optogenetic inhibitor Jaws enables the modulation of neural activity deep inside the brain.

A protein code to target RNA
The protein-RNA specificity code of an RNA-binding protein can be used to target diverse transcripts in the cell for regulation.

Unraveling the lncRNA mystery
A method to study the domain architecture of long noncoding RNAs provides insights into their biological functions.

Hitting the mark
Genome-editing technologies generally stay on target, but researchers should remain vigilant for variants acquired during experimental manipulation.

Methods in Brief

Abnormalities during reprogramming | Following transcription in real time | Intracellular topology | Identifying genetic barriers to reprogramming

Tools in Brief

Watching auxin make its move | Pinpointing postsynaptic partners | Another hit to the gut microbiome | Myelination in arrays

Methods
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Commentaries

Top

Improved reproducibility by assuring confidence in measurements in biomedical research   pp895 - 898
Anne L Plant, Laurie E Locascio, Willie E May and Patrick D Gallagher
doi:10.1038/nmeth.3076
'Irreproducibility' is symptomatic of a broader challenge in measurement in biomedical research. From the US National Institute of Standards and Technology (NIST) perspective of rigorous metrology, reproducibility is only one aspect of establishing confidence in measurements. Appropriate controls, reference materials, statistics and informatics are required for a robust measurement process. Research is required to establish these tools for biological measurements, which will lead to greater confidence in research results.

A critique of methods for temperature imaging in single cells   pp899 - 901
Guillaume Baffou, Hervé Rigneault, Didier Marguet and Ludovic Jullien
doi:10.1038/nmeth.3073
We argue that standard thermodynamic considerations and scaling laws show that a single cell cannot substantially raise its temperature by endogenous thermogenesis. This statement seriously questions the interpretations of recent work reporting temperature heterogeneities measured in single living cells.

Technology Feature

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Structural biology: 'seeing' crystals the XFEL way   pp903 - 908
Vivien Marx
doi:10.1038/nmeth.3070
X-ray free-electron lasers (XFELs) offer opportunities beyond classic X-ray crystallography, particularly for proteins that are difficult to crystallize.

News and Views

Top

Analyzing neural data at huge scale   pp911 - 912
John P Cunningham
doi:10.1038/nmeth.3071
A new distributed computing framework for data analysis enables neuroscientists to meet the computational demands of modern experimental technologies.

See also: Correspondence by Vladimirov et al. | Article by Amat et al. | Article by Freeman et al.

Brief Communications

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Efficient CRISPR-Cas9-mediated genome editing in Plasmodium falciparum   pp915 - 918
Jeffrey C Wagner, Randall J Platt, Stephen J Goldfless, Feng Zhang and Jacquin C Niles
doi:10.1038/nmeth.3063
Single guide RNAs driven by a T7 promoter target Cas9 to two endogenous loci, leading to fast and efficient genome editing in the malaria parasite P. falciparum.

High-resolution reconstruction of the beating zebrafish heart   pp919 - 922
Michaela Mickoleit, Benjamin Schmid, Michael Weber, Florian O Fahrbach, Sonja Hombach et al.
doi:10.1038/nmeth.3037
A series of technical and analytical improvements to light sheet microscopy is described, permitting dynamic imaging of the beating zebrafish heart at cellular resolution.

Visualizing a protein quake with time-resolved X-ray scattering at a free-electron laser   pp923 - 926
David Arnlund, Linda C Johansson, Cecilia Wickstrand, Anton Barty, Garth J Williams et al.
doi:10.1038/nmeth.3067
A 'protein quake' is directly monitored on the picosecond timescale using the method of time-resolved wide-angle X-ray scattering at an X-ray free-electron laser.

High-resolution structure determination by continuous-rotation data collection in MicroED   pp927 - 930
Brent L Nannenga, Dan Shi, Andrew G W Leslie and Tamir Gonen
doi:10.1038/nmeth.3043
High-resolution, three-dimensional protein structures can be solved using MicroED, an electron diffraction method that uses three-dimensional microcrystals. An improved MicroED data collection approach described here increases data quality and resolution and extends its broad applicability.

Nanoscale high-content analysis using compositional heterogeneities of single proteoliposomes   pp931 - 934
Signe Mathiasen, Sune M Christensen, Juan José Fung, Søren G F Rasmussen, Jonathan F Fay et al.
doi:10.1038/nmeth.3062
The compositional heterogeneity of proteoliposome reconstitution can skew the results of ensemble-average measurements of transmembrane protein structure and function. These compositional heterogeneities can be exploited, however, with a single-proteoliposome, high-content screening method.

Phen-Gen: combining phenotype and genotype to analyze rare disorders   pp935 - 937
Asif Javed, Saloni Agrawal and Pauline C Ng
doi:10.1038/nmeth.3046
To find causative mutations in rare disorders, the Phen-Gen software combines disease symptoms and sequencing data with prior knowledge about the gene.

Epiviz: interactive visual analytics for functional genomics data   pp938 - 940
Florin Chelaru, Llewellyn Smith, Naomi Goldstein and Héctor Corrada Bravo
doi:10.1038/nmeth.3038
Integration of genome visualization with Bioconductor-based analysis tools allows rapid and interactive analysis of genomes, transcriptomes and epigenomes.

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Articles

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Mapping brain activity at scale with cluster computing   pp941 - 950
Jeremy Freeman, Nikita Vladimirov, Takashi Kawashima, Yu Mu, Nicholas J Sofroniew et al.
doi:10.1038/nmeth.3041
An open-source library of analytical tools for mapping large-scale patterns of brain activity using cluster computing finds structure in two-photon imaging data from mouse and whole-brain light-sheet functional imaging data from behaving larval zebrafish. Vladimirov et al., also in this issue, describes the light-sheet functional imaging system used here.

See also: News and Views by Cunningham

Fast, accurate reconstruction of cell lineages from large-scale fluorescence microscopy data   pp951 - 958
Fernando Amat, William Lemon, Daniel P Mossing, Katie McDole, Yinan Wan et al.
doi:10.1038/nmeth.3036
This paper describes automated methods for the accurate segmentation and tracking of tens of thousands of nuclei in time-lapse imaging data of developing embryos.

See also: News and Views by Cunningham

RNA motif discovery by SHAPE and mutational profiling (SHAPE-MaP)   pp959 - 965
Nathan A Siegfried, Steven Busan, Greggory M Rice, Julie A E Nelson and Kevin M Weeks
doi:10.1038/nmeth.3029
The combination of selective 2'-hydroxyl acylation of RNA with high-throughput sequencing of the transcribed cDNA allows identification of chemically modified sites as mutations in the sequence that then yield highly accurate secondary-structure models of the RNA.

Isolation of rare recombinants without using selectable markers for one-step seamless BAC mutagenesis   pp966 - 970
George T Lyozin, Paul C Bressloff, Amit Kumar, Yasuhiro Kosaka, Bradley L Demarest et al.
doi:10.1038/nmeth.3030
Application of the founder principle from population genetics to variant selection after recombineering allows the isolation of rare unselected recombinants.

Addendum

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Addendum: Independent optical excitation of distinct neural populations   p972
Nathan C Klapoetke, Yasunobu Murata, Sung Soo Kim, Stefan R Pulver, Amanda Birdsey-Benson et al.
doi:10.1038/nmeth0914-972

Corrigenda

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Corrigendum: Fluorophore localization algorithms for super-resolution microscopy   p971
Alex Small and Shane Stahlheber
doi:10.1038/nmeth0914-971a

Corrigendum: Evaluation of quantitative miRNA expression platforms in the microRNA quality control (miRQC) study   p971
Pieter Mestdagh, Nicole Hartmann, Lukas Baeriswyl, Ditte Andreasen, Nathalie Bernard et al.
doi:10.1038/nmeth0914-971b

Corrigendum: A holidic medium for Drosophila melanogaster   p971
Matthew D W Piper, Eric Blanc, Ricardo Leitão-Goncalves, Mingyao Yang, Xiaoli He et al.
doi:10.1038/nmeth0914-971c

Corrigendum: Independent optical excitation of distinct neural populations   p971
Nathan C Klapoetke, Yasunobu Murata, Sung Soo Kim, Stefan R Pulver, Amanda Birdsey-Benson et al.
doi:10.1038/nmeth0914-971d

Application Notes

Top

Chromatrap® 96: a new solid-state platform for high-throughput ChIP   
Amy L Beynon, Lindsay J Parkes, Matthew L Turner, Steve Knight, Steve Conlan et al.

One solution for cloning and mutagenesis: In-Fusion® HD Cloning Plus   
Malathi Raman and Karen Martin

Top
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