Thursday, November 8, 2018

Nature Methods Contents: November 2018, Volume 15 No 11

Nature Methods


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TABLE OF CONTENTS

November 2018 Volume 15, Issue 11

Editorial
This Month
Correspondence
Comment
Research Highlights
Technology Feature
News & Views
Review Articles
Resources
Brief Communications
Articles
Amendments & Corrections

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Editorial

The impact of the NIH BRAIN Initiative    p839
doi:10.1038/s41592-018-0210-0

This Month

Anna Moroni    p841
Vivien Marx
doi:10.1038/s41592-018-0192-y

Predicting with confidence and tolerance    pp843 - 845
Naomi Altman & Martin Krzywinski
doi:10.1038/s41592-018-0196-7

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Correspondence

A community-developed open-source computational ecosystem for big neuro data    pp846 - 847
Joshua T. Vogelstein, Eric Perlman, Benjamin Falk, Alex Baden, William Gray Roncal et al.
doi:10.1038/s41592-018-0181-1

Striped UniFrac: enabling microbiome analysis at unprecedented scale    pp847 - 848
Daniel McDonald, Yoshiki Vázquez-Baeza, David Koslicki, Jason McClelland, Nicolai Reeve et al.
doi:10.1038/s41592-018-0187-8

Comment

A call for public archives for biological image data    pp849 - 854
Jan Ellenberg, Jason R. Swedlow, Mary Barlow, Charles E. Cook, Ugis Sarkans et al.
doi:10.1038/s41592-018-0195-8

Research Highlights

High-speed protein crystallography    p855
Allison Doerr
doi:10.1038/s41592-018-0205-x

Fluorescent proteins from scratch    p856
Rita Strack
doi:10.1038/s41592-018-0206-9

Keeping CRISPR in check    p857
Nicole Rusk
doi:10.1038/s41592-018-0207-8

Diploid genome in 3D    p858
Lei Tang
doi:10.1038/s41592-018-0208-7

A winning single-cell combination    p859
Tal Nawy
doi:10.1038/s41592-018-0197-6

Smarter cell sorting    p859
Rita Strack
doi:10.1038/s41592-018-0198-5

Shaking up clearing cocktails    p859
Nina Vogt
doi:10.1038/s41592-018-0199-4

Finding S-sulfinylated proteins    p859
Allison Doerr
doi:10.1038/s41592-018-0200-2

Protein circuit engineering    p860
Nicole Rusk
doi:10.1038/s41592-018-0201-1

Mechanistic microbiota models    p860
Tal Nawy
doi:10.1038/s41592-018-0202-0

Blinking in the cold    p860
Rita Strack
doi:10.1038/s41592-018-0203-z

Improving long-read accuracy    p860
Lei Tang
doi:10.1038/s41592-018-0204-y

Variants from the deep    p861
Tal Nawy
doi:10.1038/s41592-018-0209-6

Technology Feature

Neuroscience models: choose your dimension    pp863 - 866
Vivien Marx
doi:10.1038/s41592-018-0191-z

News & Views

Enhancing the glycosciences toolkit: new GAGs in the lineup    pp867 - 868
Jeremy E. Turnbull
doi:10.1038/s41592-018-0190-0

Deep learning to predict microscope images    pp868 - 870
Roger Brent & Laura Boucheron
doi:10.1038/s41592-018-0194-9

Review Articles

Cellular barcoding: lineage tracing, screening and beyond    pp871 - 879
Justus M. Kebschull & Anthony M. Zador
doi:10.1038/s41592-018-0185-x

A review of cellular barcoding fundamentals and applications, including powerful approaches for lineage reconstruction, genetic screening, and the recording of cellular activity and neuroanatomy.

Resources

The GAGOme: a cell-based library of displayed glycosaminoglycans    pp881 - 888
Yen-Hsi Chen, Yoshiki Narimatsu, Thomas M. Clausen, Catarina Gomes, Richard Karlsson et al.
doi:10.1038/s41592-018-0086-z

A CHO cell library displaying a near-complete repertoire of glycosaminoglycan (GAG) modifications provides a resource for cell-based binding assays, recombinant proteoglycan expression, and assembly of GAG glycan microarrays.

A mutant-cell library for systematic analysis of heparan sulfate structure–function relationships    pp889 - 899
Hong Qiu, Songshan Shi, Jingwen Yue, Meng Xin, Alison V. Nairn et al.
doi:10.1038/s41592-018-0189-6

A library of mutant mouse lung endothelial cells expressing a comprehensive repertoire of heparin sulfate structure modifications enables studies of the structure–function relationships of this complex polysaccharide.

Brief Communications

The hit-and-return system enables efficient time-resolved serial synchrotron crystallography    pp901 - 904
Eike C. Schulz, Pedram Mehrabi, Henrike M. Müller-Werkmeister, Friedjof Tellkamp, Ajay Jha et al.
doi:10.1038/s41592-018-0180-2

A data-collection strategy using a fixed-target crystallography chip allows time-resolved serial synchrotron crystallography experiments to determine enzyme intermediate structures with time resolutions of milliseconds to seconds.

A fully automatic method yielding initial models from high-resolution cryo-electron microscopy maps    pp905 - 908
Thomas C. Terwilliger, Paul D. Adams, Pavel V. Afonine & Oleg V. Sobolev
doi:10.1038/s41592-018-0173-1

A fully automated method for modeling protein and protein–RNA complex structure from cryo-EM data, requiring minimal user intervention, is described.

A high-throughput pipeline for validation of antibodies    pp909 - 912
Krzysztof Sikorski, Adi Mehta, Marit Inngjerdingen, Flourina Thakor, Simon Kling et al.
doi:10.1038/s41592-018-0179-8

This paper describes a platform for carrying out antibody-based capture and mass spectrometry in parallel, and tests the feasibility of this platform for high-throughput validation of antibodies.

Analyzing complex single-molecule emission patterns with deep learning    pp913 - 916
Peiyi Zhang, Sheng Liu, Abhishek Chaurasia, Donghan Ma, Michael J. Mlodzianoski et al.
doi:10.1038/s41592-018-0153-5

The deep neural network smNet extracts multiplexed parameters such as 3D position, orientation and wavefront distortion from emission patterns of single molecules.

Label-free prediction of three-dimensional fluorescence images from transmitted-light microscopy    pp917 - 920
Chawin Ounkomol, Sharmishtaa Seshamani, Mary M. Maleckar, Forrest Collman & Gregory R. Johnson
doi:10.1038/s41592-018-0111-2

Convolutional neural networks enable prediction of fluorescently labeled structures from three-dimensional time-lapse transmitted-light images. Applications include multiplexed long time-lapse imaging and prediction of fluorescence in electron micrographs.

FLIRT: fast local infrared thermogenetics for subcellular control of protein function    pp921 - 923
Sophia M. Hirsch, Sriramkumar Sundaramoorthy, Tim Davies, Yelena Zhuravlev, Jennifer C. Waters et al.
doi:10.1038/s41592-018-0168-y

FLIRT enables spatiotemporally precise control of protein function in C. elegans by harnessing existing temperature-sensitive mutations. Proteins can be inactivated at desired sites by infrared laser light targeted to the region(s) of interest.

Engineered anti-CRISPR proteins for optogenetic control of CRISPR–Cas9    pp924 - 927
Felix Bubeck, Mareike D. Hoffmann, Zander Harteveld, Sabine Aschenbrenner, Andreas Bietz et al.
doi:10.1038/s41592-018-0178-9

CASANOVA uses LOV and blue light to regulate CRISPR activity.

CRISPR-Sirius: RNA scaffolds for signal amplification in genome imaging    pp928 - 931
Hanhui Ma, Li-Chun Tu, Ardalan Naseri, Yu-Chieh Chung, David Grunwald et al.
doi:10.1038/s41592-018-0174-0

Multiple MS2 loops inserted in the first loop of an sgRNA after the spacer sequence stabilize the sgRNA and allow recruitment of multicolor fluorescent proteins for imaging of low-repeat genomic loci.

Spatial organization of the somatosensory cortex revealed by osmFISH    pp932 - 935
Simone Codeluppi, Lars E. Borm, Amit Zeisel, Gioele La Manno, Josina A. van Lunteren et al.
doi:10.1038/s41592-018-0175-z

osmFISH applies automated cycles of single-molecule fluorescence in situ hybridization without barcoding to provide spatial gene expression in tissue sections at high sensitivity, accuracy and throughput.

Stability, affinity, and chromatic variants of the glutamate sensor iGluSnFR    pp936 - 939
Jonathan S. Marvin, Benjamin Scholl, Daniel E. Wilson, Kaspar Podgorski, Abbas Kazemipour et al.
doi:10.1038/s41592-018-0171-3

Variants of the genetically encoded sensor iGluSnFR extend the range of conditions under which glutamate neurotransmission can be visualized. In addition, chromatic variants of iGluSnFR improve compatibility with various illumination schemes.

Articles

Guide Swap enables genome-scale pooled CRISPR–Cas9 screening in human primary cells    pp941 - 946
Pamela Y. Ting, Albert E. Parker, J. Scott Lee, Chris Trussell, Orzala Sharif et al.
doi:10.1038/s41592-018-0149-1

Guide Swap challenges the hypothesis that Cas9–sgRNA binding is irreversible. The authors find that instead, nontargeting sgRNAs are swapped for targeting sgRNAs in the Cas9 complex. The method allows genome-scale functional screens in primary cells

De novo computational RNA modeling into cryo-EM maps of large ribonucleoprotein complexes    pp947 - 954
Kalli Kappel, Shiheng Liu, Kevin P. Larsen, Georgios Skiniotis, Elisabetta Viani Puglisi et al.
doi:10.1038/s41592-018-0172-2

DRRAFTER, a method for RNA modeling into cryo-EM maps, generates accurate models for diverse RNA–protein complexes.

emClarity: software for high-resolution cryo-electron tomography and subtomogram averaging    pp955 - 961
Benjamin A. Himes & Peijun Zhang
doi:10.1038/s41592-018-0167-z

A software tool, emClarity, implements several improvements in cryo-electron tomography image-processing algorithms to achieve sub-nanometer resolution for diverse macromolecular structures.

Species-level functional profiling of metagenomes and metatranscriptomes    pp962 - 968
Eric A. Franzosa, Lauren J. McIver, Gholamali Rahnavard, Luke R. Thompson, Melanie Schirmer et al.
doi:10.1038/s41592-018-0176-y

HUMAnN2 uses a tiered sequence search to provide rapid and accurate species-level functional profiles of microbial communities from metagenomic and metatranscriptomic data.

A light-gated potassium channel for sustained neuronal inhibition    pp969 - 976
Laura Alberio, Andrea Locarno, Andrea Saponaro, Edoardo Romano, Valérie Bercier et al.
doi:10.1038/s41592-018-0186-9

BLINK2 is a light-activated potassium channel for optogenetic inhibition of neuronal activity. Alberio et al. apply the tool in systems as diverse as cultured rat neurons, mouse brain slices, behaving zebrafish and a rat model of neuropathic pain.

Transparent Danionella translucida as a genetically tractable vertebrate brain model    pp977 - 983
Lisanne Schulze, Jörg Henninger, Mykola Kadobianskyi, Thomas Chaigne, Ana Isabel Faustino et al.
doi:10.1038/s41592-018-0144-6

The combination of transparency, small brain size and genetic access positions Danionella translucida as a promising model organism for functional imaging of neuronal circuits, especially during complex behaviors in adults.

Amendments & Corrections

Publisher Correction: Image Data Resource: a bioimage data integration and publication platform    p984
Eleanor Williams, Josh Moore, Simon W Li, Gabriella Rustici, Aleksandra Tarkowska et al.
doi:10.1038/s41592-018-0169-x

Publisher Correction: Precision and accuracy of single-molecule FRET measurements—a multi-laboratory benchmark study    p984
Björn Hellenkamp, Sonja Schmid, Olga Doroshenko, Oleg Opanasyuk, Ralf Kühnemuth et al.
doi:10.1038/s41592-018-0193-x

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