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TABLE OF CONTENTS |
May 2016 Volume 13, Issue 5 |
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| In This Issue Editorial This Month Correspondence Research Highlights Technology Feature Reviews 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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Data sharing comes to structural biology p381 doi:10.1038/nmeth.3862 New archives for raw X-ray crystallography and cryo-EM data will accelerate progress in structural biology.
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This Month | Top |
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The Author File: Judit Villen p383 Vivien Marx doi:10.1038/nmeth.3841 Measuring phosphoproteins reproducibly and taking time to bike.
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Points of Significance: Regression diagnostics pp385 - 386 Naomi Altman and Martin Krzywinski doi:10.1038/nmeth.3854 Residual plots can be used to validate assumptions about the regression model.
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Correspondence | Top |
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EMPIAR: a public archive for raw electron microscopy image data pp387 - 388 Andrii Iudin, Paul K Korir, José Salavert-Torres, Gerard J Kleywegt and Ardan Patwardhan doi:10.1038/nmeth.3806
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Research Highlights | Top |
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Technology Feature | Top |
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Microbiology: the road to strain-level identification pp401 - 404 Vivien Marx doi:10.1038/nmeth.3837 Tools are emerging to help labs trawl for sequences that reveal microbial strains and their functional potential in deep pools of metagenomic data.
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Reviews | Top |
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A practical guide to hydrogels for cell culture pp405 - 414 Steven R Caliari and Jason A Burdick doi:10.1038/nmeth.3839
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Measuring cell-generated forces: a guide to the available tools pp415 - 423 William J Polacheck and Christopher S Chen doi:10.1038/nmeth.3834 There is a growing appreciation that mechanical forces have important roles in many aspects of biology. This review provides a survey of methods for measuring the forces exerted by cells and discusses technical barriers to their implementation.
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Analysis | Top |
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Standardized benchmarking in the quest for orthologs OPEN pp425 - 430 Adrian M Altenhoff, Brigitte Boeckmann, Salvador Capella-Gutierrez, Daniel A Dalquen, Todd DeLuca et al. doi:10.1038/nmeth.3830
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Brief Communications | Top |
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Plug-and-play analysis of the human phosphoproteome by targeted high-resolution mass spectrometry pp431 - 434 Robert T Lawrence, Brian C Searle, Ariadna Llovet and Judit Villén doi:10.1038/nmeth.3811 A method (and resource) demonstrating the mining of information from large-scale phosphoproteomics data sets is presented, allowing users to build targeted parallel reaction monitoring mass spectrometry assays to study phosphosites of interest.
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Strain-level microbial epidemiology and population genomics from shotgun metagenomics pp435 - 438 Matthias Scholz, Doyle V Ward, Edoardo Pasolli, Thomas Tolio, Moreno Zolfo et al. doi:10.1038/nmeth.3802 PanPhlAn detects strains and characterizes strain-specific gene content and activity within metagenomic and metatranscriptomic samples for microbial population analysis and epidemiology.
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Quantitative super-resolution imaging with qPAINT pp439 - 442 Ralf Jungmann, Maier S Avendaño, Mingjie Dai, Johannes B Woehrstein, Sarit S Agasti et al. doi:10.1038/nmeth.3804 Quantitative points accumulation in nanoscale topography (qPAINT) makes use of predictable binding kinetics between DNA-PAINT imager and docking strands to achieve accurate and precise counting of molecules in spatially unresolved complexes.
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Sparse PCA corrects for cell type heterogeneity in epigenome-wide association studies pp443 - 445 Elior Rahmani, Noah Zaitlen, Yael Baran, Celeste Eng, Donglei Hu et al. doi:10.1038/nmeth.3809 Principal component analysis on a subset of differentially methylated regions in a mixture of cell types is the basis of ReFACTor, a program to account for heterogeneity in epigenome-wide association studies (EWAS).
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Articles | Top |
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High-efficiency cellular reprogramming with microfluidics pp446 - 452 Camilla Luni, Stefano Giulitti, Elena Serena, Luca Ferrari, Alessandro Zambon et al. doi:10.1038/nmeth.3832 Microfluidic reprogramming of human somatic cells to induced pluripotent stem cells is rapid and highly efficient, enabling large-scale derivation from patient cells as well as seamless on-chip differentiation without cell expansion.
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Reprogramming eukaryotic translation with ligand-responsive synthetic RNA switches pp453 - 458 Andrew V Anzalone, Annie J Lin, Sakellarios Zairis, Raul Rabadan and Virginia W Cornish doi:10.1038/nmeth.3807 Ligand-triggered ribosomal frameshifting allows control of the relative stoichiometry of two proteins and enables the building of logic gates from a single mRNA.
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