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Method of the Year 2013.
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- Nature Methods, 2014, v. 11, n. 1, p. 1, doi. 10.1038/nmeth.2801
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Benjamin F. Cravatt.
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- Nature Methods, 2014, v. 11, n. 1, p. 3, doi. 10.1038/nmeth.2774
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Genomics: Genomes in 3D improve one-dimensional assemblies.
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- Nature Methods, 2014, v. 11, n. 1, p. 5, doi. 10.1038/nmeth.2795
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Structural biology: Electron crystallography goes 3D WITH MicroED.
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- Nature Methods, 2014, v. 11, n. 1, p. 6, doi. 10.1038/nmeth.2797
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Biophysics: Unfolding to force.
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- Nature Methods, 2014, v. 11, n. 1, p. 6, doi. 10.1038/nmeth.2796
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Sequencing: Protein nanopores to detect DNA methylation.
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- Nature Methods, 2014, v. 11, n. 1, p. 8, doi. 10.1038/nmeth.2798
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Sequencing: Transcriptome of a single nucleus.
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- Nature Methods, 2014, v. 11, n. 1, p. 9, doi. 10.1038/nmeth.2788
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Molecular engineering: Engineering detergent-stable membrane proteins.
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- Nature Methods, 2014, v. 11, n. 1, p. 9, doi. 10.1038/nmeth.2789
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- Article
Genomics: Bias in ChIP-seq data.
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- Nature Methods, 2014, v. 11, n. 1, p. 9, doi. 10.1038/nmeth.2786
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Structural biology: A solution to the phasing problem.
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- Nature Methods, 2014, v. 11, n. 1, p. 9, doi. 10.1038/nmeth.2787
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Genetics: TALENs knock out human microRNAs.
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- Nature Methods, 2014, v. 11, n. 1, p. 10, doi. 10.1038/nmeth.2792
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Chemical biology: Chemically probing GPCR-ligand interactions.
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- Nature Methods, 2014, v. 11, n. 1, p. 10, doi. 10.1038/nmeth.2790
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Neuroscience: Seeing the brain through a prism.
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- Nature Methods, 2014, v. 11, n. 1, p. 10, doi. 10.1038/nmeth.2793
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Stem cells: 3D expansion of human pluripotent stem cells.
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- Nature Methods, 2014, v. 11, n. 1, p. 10, doi. 10.1038/nmeth.2791
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Structural biology: The in vivo RNA structurome.
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- Nature Methods, 2014, v. 11, n. 1, p. 11, doi. 10.1038/nmeth.2799
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Singled out for sequencing.
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- Nature Methods, 2014, v. 11, n. 1, p. 13, doi. 10.1038/nmeth.2768
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Single-cell sequencing.
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- Nature Methods, 2014, v. 11, n. 1, p. 18, doi. 10.1038/nmeth.2771
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Dissecting genomic diversity, one cell at a time.
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- Nature Methods, 2014, v. 11, n. 1, p. 19, doi. 10.1038/nmeth.2783
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Entering the era of single-cell transcriptomics in biology and medicine.
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- Nature Methods, 2014, v. 11, n. 1, p. 22, doi. 10.1038/nmeth.2764
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The promise of single-cell sequencing.
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- Nature Methods, 2014, v. 11, n. 1, p. 25, doi. 10.1038/nmeth.2769
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Bring on the neuro tools.
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- Nature Methods, 2014, v. 11, n. 1, p. 28, doi. 10.1038/nmeth.2776
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CRISPRs and epigenome editing.
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- Nature Methods, 2014, v. 11, n. 1, p. 28, doi. 10.1038/nmeth.2775
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Tiny tools to measure force.
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- Nature Methods, 2014, v. 11, n. 1, p. 29, doi. 10.1038/nmeth.2778
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In situ sequencing.
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- Nature Methods, 2014, v. 11, n. 1, p. 29, doi. 10.1038/nmeth.2777
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Single-particle electron cryomicroscopy.
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- Nature Methods, 2014, v. 11, n. 1, p. 30, doi. 10.1038/nmeth.2779
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Intracellular mini-binders.
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- Nature Methods, 2014, v. 11, n. 1, p. 30, doi. 10.1038/nmeth.2780
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Self-organizing stem cells.
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- Nature Methods, 2014, v. 11, n. 1, p. 31, doi. 10.1038/nmeth.2782
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The power of a crowd.
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- Nature Methods, 2014, v. 11, n. 1, p. 31, doi. 10.1038/nmeth.2781
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Pouring over liquid handling.
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- Nature Methods, 2014, v. 11, n. 1, p. 33, doi. 10.1038/nmeth.2785
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The genome shows its sensitive side.
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- Nature Methods, 2014, v. 11, n. 1, p. 39, doi. 10.1038/nmeth.2770
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Quantitative assessment of single-cell RNA-sequencing methods.
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- Nature Methods, 2014, v. 11, n. 1, p. 41, doi. 10.1038/nmeth.2694
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A quantitative liposome microarray to systematically characterize protein-lipid interactions.
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- Nature Methods, 2014, v. 11, n. 1, p. 47, doi. 10.1038/nmeth.2734
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Quantifying RNA allelic ratios by microfluidic multiplex PCR and sequencing.
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- Nature Methods, 2014, v. 11, n. 1, p. 51, doi. 10.1038/nmeth.2736
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Deciphering laminar-specific neural inputs with line-scanning fMRI.
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- Nature Methods, 2014, v. 11, n. 1, p. 55, doi. 10.1038/nmeth.2730
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HiRIEF LC-MS enables deep proteome coverage and unbiased proteogenomics.
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- Nature Methods, 2014, v. 11, n. 1, p. 59, doi. 10.1038/nmeth.2732
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Quantifying the local resolution of cryo-EM density maps.
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- Nature Methods, 2014, v. 11, n. 1, p. 63, doi. 10.1038/nmeth.2727
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Coupling transcription factor occupancy to nucleosome architecture with DNase-FLASH.
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- Nature Methods, 2014, v. 11, n. 1, p. 66, doi. 10.1038/nmeth.2713
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Refined DNase-seq protocol and data analysis reveals intrinsic bias in transcription factor footprint identification.
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- Nature Methods, 2014, v. 11, n. 1, p. 73, doi. 10.1038/nmeth.2762
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A chemoproteomic platform to quantitatively map targets of lipid-derived electrophiles.
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- Nature Methods, 2014, v. 11, n. 1, p. 79, doi. 10.1038/nmeth.2759
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Parallel measurement of dynamic changes in translation rates in single cells.
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- Nature Methods, 2014, v. 11, n. 1, p. 86, doi. 10.1038/nmeth.2729
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Integrating protein-protein interaction networks with phenotypes reveals signs of interactions.
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- Nature Methods, 2014, v. 11, n. 1, p. 94, doi. 10.1038/nmeth.2733
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A holidic medium for Drosophila melanogaster.
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- Nature Methods, 2014, v. 11, n. 1, p. 100, doi. 10.1038/nmeth.2731
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Niche-independent high-purity cultures of Lgr5<sup>+</sup> intestinal stem cells and their progeny.
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- Nature Methods, 2014, v. 11, n. 1, p. 106, doi. 10.1038/nmeth.2737
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