Thursday, July 5, 2018

Nature Methods Contents: July 2018, Volume 15 No 7

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Nature Methods
TABLE OF CONTENTS

July 2018 Volume 15, Issue 7

Editorial
This Month
Correspondence
Research Highlights
Technology Feature
News & Views
Analysis
Brief Communications
Articles
Amendments & Corrections
 
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Custom Media presents a webcast on: Combining scRNA-seq and Flow Analyses
 
Date: Tuesday, July 24, 2018
 
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Nature Index 2018 Japan

Some of Japan's smallest institutions are among the most efficient in the production of high quality scientific research, though the decline in Japan's high quality scientific research output continues. This supplement examines reform efforts in light of the country's aim to become a "super-smart" society. 

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Editorial

 

US universities go East    p471
doi:10.1038/s41592-018-0060-9

This Month

 

John T. Ngo    p473
Vivien Marx
doi:10.1038/s41592-018-0047-6

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Nature Spotlight on Hong Kong: Building science innovation 

Hong Kong is maximising major scientific innovation and commercial benefits through its proximity to the research and development hubs in mainland China. Yet barriers to collaboration remain. 

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Correspondence

 

Bioconda: sustainable and comprehensive software distribution for the life sciences    pp475 - 476
Björn Grüning, Ryan Dale, Andreas Sjödin, Brad A. Chapman, Jillian Rowe et al.
doi:10.1038/s41592-018-0046-7

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Research Highlights

 

Weighing single proteins with light    p477
Rita Strack
doi:10.1038/s41592-018-0055-6

Corrected in vivo imaging    p478
Zachary J. Lapin
doi:10.1038/s41592-018-0056-5

Correlating behavior and neural activity at high resolution    p479
Nina Vogt
doi:10.1038/s41592-018-0057-4

Transcripts from a spliceosome    p480
Tal Nawy
doi:10.1038/s41592-018-0058-3

Targeting Cas9    p481
Nicole Rusk
doi:10.1038/s41592-018-0061-8

Sensing cellular metabolites    p481
Rita Strack
doi:10.1038/s41592-018-0062-7

Higher-order genetic interactions    p481
Nicole Rusk
doi:10.1038/s41592-018-0063-6

Inferring neuronal activity from gene expression    p481
Nina Vogt
doi:10.1038/s41592-018-0064-5

Speedy optogenetics in red    p482
Nina Vogt
doi:10.1038/s41592-018-0065-4

DNA molecular forceps    p482
Allison Doerr
doi:10.1038/s41592-018-0066-3

Metastasis in a dish    p482
Tal Nawy
doi:10.1038/s41592-018-0067-2

Clocking translation in live cells    p482
Rita Strack
doi:10.1038/s41592-018-0068-1

Polymer model predicts chromatin folding    p483
Lei Tang
doi:10.1038/s41592-018-0059-2

Methods
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Technology Feature

 

What makes birds and bats the talk of the town    pp485 - 488
Vivien Marx
doi:10.1038/s41592-018-0050-y

News & Views

 

Controlling protein function with HCV protease    pp489 - 490
Bryan C. Dickinson
doi:10.1038/s41592-018-0043-x

Analysis

 

A comparison of methods to assess cell mechanical properties    pp491 - 498
Pei-Hsun Wu, Dikla Raz-Ben Aroush, Atef Asnacios, Wei-Chiang Chen, Maxim E. Dokukin et al.
doi:10.1038/s41592-018-0015-1

This Analysis compares and contrasts methods for measuring the mechanical properties of cells by applying the different approaches to the same breast cancer cell line.

 

A reassessment of DNA-immunoprecipitation-based genomic profiling    pp499 - 504
Antonio Lentini, Cathrine Lagerwall, Svante Vikingsson, Heidi K. Mjoseng, Karolos Douvlataniotis et al.
doi:10.1038/s41592-018-0038-7

Reanalysis of DNA-immunoprecipitation-based data shows that modification-specific antibodies bind unmodified short tandem repeats, and IgG controls are needed to avoid false positives.

 

Comprehensive comparative analysis of 5′-end RNA-sequencing methods    pp505 - 511
Xian Adiconis, Adam L. Haber, Sean K. Simmons, Ami Levy Moonshine, Zhe Ji et al.
doi:10.1038/s41592-018-0014-2

A direct comparison of 5′-end RNA-seq methods reveals strong performance by CAGE, and identifies differential transcriptional start site usage among brain-related samples.

 

Brief Communications

 

CRISPR off-target analysis in genetically engineered rats and mice    pp512 - 514
Keith R. Anderson, Maximilian Haeussler, Colin Watanabe, Vasantharajan Janakiraman, Jessica Lund et al.
doi:10.1038/s41592-018-0011-5

Off-targets identified by whole-genome sequencing of CRISPR-treated mouse embryos and their genetic parents are compared to predictions from GUIDE-seq and computational methods.

 

Automated, parallel mass spectrometry imaging and structural identification of lipids    pp515 - 518
Shane R. Ellis, Martin R. L. Paine, Gert B. Eijkel, Josch K. Pauling, Peter Husen et al.
doi:10.1038/s41592-018-0010-6

An automated method coupling tandem mass spectrometry with high-resolution mass spectrometry imaging simultaneously reveals both the molecular structure of lipids and their spatial locations in tissue.

 

Chemogenetic control of gene expression and cell signaling with antiviral drugs    pp519 - 522

doi:10.1038/s41592-018-0042-y

Ligand-inducible connection (LInC) combines HCV protease and protease inhibitors to offer an orthogonal chemogenetic approach for controlling protein functions including protein localization, gene expression, and cell–cell communication.

 

StaPLs: versatile genetically encoded modules for engineering drug-inducible proteins    pp523 - 526
Conor L. Jacobs, Ryan K. Badiee & Michael Z. Lin
doi:10.1038/s41592-018-0041-z

Stabilizable polypeptide linkages (StaPLs) based on hepatitis C virus protease enable robust, reversible, and orthogonal chemogenetic control of protein functions, including CRISPR–Cas9 activity, transcription, and protein dimerization.

 

EASI-tag enables accurate multiplexed and interference-free MS2-based proteome quantification    pp527 - 530
Sebastian Virreira Winter, Florian Meier, Christoph Wichmann, Juergen Cox, Matthias Mann et al.
doi:10.1038/s41592-018-0037-8

EASI-tag, a new type of isobaric labeling reagents, enables multiplexed and highly accurate proteome quantification by mass spectrometry.

 

DeTiN: overcoming tumor-in-normal contamination    pp531 - 534
Amaro Taylor-Weiner, Chip Stewart, Thomas Giordano, Mendy Miller, Mara Rosenberg et al.
doi:10.1038/s41592-018-0036-9

DeTiN can identify and account for signal from tumor cells that contaminate normal samples, for more sensitive somatic variant detection.

 

Efficient and precise editing of endogenous transcripts with SNAP-tagged ADARs    pp535 - 538
Paul Vogel, Matin Moschref, Qin Li, Tobias Merkle, Karthika D. Selvasaravanan et al.
doi:10.1038/s41592-018-0017-z

Fusion of a guide RNA directly to an adenosine deaminase via a SNAP-tag allows for precise and efficient RNA editing.

 

SAVER: gene expression recovery for single-cell RNA sequencing    pp539 - 542
Mo Huang, Jingshu Wang, Eduardo Torre, Hannah Dueck, Sydney Shaffer et al.
doi:10.1038/s41592-018-0033-z

SAVER accurately recovers expression values in single-cell RNA-sequencing data to improve downstream analysis.

 

GeNets: a unified web platform for network-based genomic analyses    pp543 - 546
Taibo Li, April Kim, Joseph Rosenbluh, Heiko Horn, Liraz Greenfeld et al.
doi:10.1038/s41592-018-0039-6

The GeNets web platform can identify the most informative network, as well as execute, store and share network-based analyses of RNA-seq or genomic datasets.

 

Articles

 

Mapping the physical network of cellular interactions    pp547 - 553
Jean-Charles Boisset, Judith Vivié, Dominic Grün, Mauro J. Muraro, Anna Lyubimova et al.
doi:10.1038/s41592-018-0009-z

The ProximID approach generates single-cell expression profiles and a network of enriched physical cellular interactions within a tissue.

 

Amendments & Corrections

 

Author Correction: Informed-Proteomics: open-source software package for top-down proteomics    p554
Jungkap Park, Paul D Piehowski, Christopher Wilkins, Mowei Zhou, Joshua Mendoza et al.
doi:10.1038/s41592-018-0040-0

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