Nature Biotechnology

Papers
(The H4-Index of Nature Biotechnology is 110. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-11-01 to 2024-11-01.)
ArticleCitations
SignalP 6.0 predicts all five types of signal peptides using protein language models1309
Nanopore sequencing technology, bioinformatics and applications824
CheckV assesses the quality and completeness of metagenome-assembled viral genomes777
Highly sensitive spatial transcriptomics at near-cellular resolution with Slide-seqV2759
Dictionary learning for integrative, multimodal and scalable single-cell analysis679
Fast and accurate protein structure search with Foldseek653
Cell2location maps fine-grained cell types in spatial transcriptomics550
Robust decomposition of cell type mixtures in spatial transcriptomics547
A genomic catalog of Earth’s microbiomes523
Spatial transcriptomics at subspot resolution with BayesSpace493
Whole-cell segmentation of tissue images with human-level performance using large-scale data annotation and deep learning438
Delineating copy number and clonal substructure in human tumors from single-cell transcriptomes431
Systematic classification of unknown metabolites using high-resolution fragmentation mass spectra408
Large language models generate functional protein sequences across diverse families405
Engineered pegRNAs improve prime editing efficiency392
The clinical progress of mRNA vaccines and immunotherapies377
Differential abundance testing on single-cell data using k-nearest neighbor graphs354
Extending and improving metagenomic taxonomic profiling with uncharacterized species using MetaPhlAn 4334
Wearable materials with embedded synthetic biology sensors for biomolecule detection333
A Python library for probabilistic analysis of single-cell omics data330
Improved metagenome binning and assembly using deep variational autoencoders329
Integrative analysis of multimodal mass spectrometry data in MZmine 3325
Mapping single-cell data to reference atlases by transfer learning308
Modular, efficient and constant-memory single-cell RNA-seq preprocessing306
inStrain profiles population microdiversity from metagenomic data and sensitively detects shared microbial strains295
High-plex imaging of RNA and proteins at subcellular resolution in fixed tissue by spatial molecular imaging292
Scalable, multimodal profiling of chromatin accessibility, gene expression and protein levels in single cells290
Single-cell CUT&Tag profiles histone modifications and transcription factors in complex tissues288
A long-term study of AAV gene therapy in dogs with hemophilia A identifies clonal expansions of transduced liver cells279
Programmable deletion, replacement, integration and inversion of large DNA sequences with twin prime editing276
Computational principles and challenges in single-cell data integration275
Generation of human striatal organoids and cortico-striatal assembloids from human pluripotent stem cells267
Carbon-negative production of acetone and isopropanol by gas fermentation at industrial pilot scale261
Pre-activated antiviral innate immunity in the upper airways controls early SARS-CoV-2 infection in children248
Readfish enables targeted nanopore sequencing of gigabase-sized genomes243
Multi-omics single-cell data integration and regulatory inference with graph-linked embedding238
Haplotype-resolved assembly of diploid genomes without parental data235
Deep Visual Proteomics defines single-cell identity and heterogeneity230
Identification of antimicrobial peptides from the human gut microbiome using deep learning228
In vivo adenine base editing of PCSK9 in macaques reduces LDL cholesterol levels226
High-efficiency prime editing with optimized, paired pegRNAs in plants221
Human heart-forming organoids recapitulate early heart and foregut development219
Spatially informed cell-type deconvolution for spatial transcriptomics218
Single-sequence protein structure prediction using a language model and deep learning215
Long-term wireless streaming of neural recordings for circuit discovery and adaptive stimulation in individuals with Parkinson’s disease215
Unlocking the promise of mRNA therapeutics212
Functional, metabolic and transcriptional maturation of human pancreatic islets derived from stem cells209
Fully implantable and bioresorbable cardiac pacemakers without leads or batteries208
Ultra-fast proteomics with Scanning SWATH205
Drag-and-drop genome insertion of large sequences without double-strand DNA cleavage using CRISPR-directed integrases202
Wireless, closed-loop, smart bandage with integrated sensors and stimulators for advanced wound care and accelerated healing198
Identifying phenotype-associated subpopulations by integrating bulk and single-cell sequencing data198
Integration of spatial and single-cell transcriptomic data elucidates mouse organogenesis198
Biopharmaceutical benchmarks 2022197
Reimagining high-throughput profiling of reactive cysteines for cell-based screening of large electrophile libraries194
CRISPR RNA-guided integrases for high-efficiency, multiplexed bacterial genome engineering193
Deep diversification of an AAV capsid protein by machine learning192
Spatial components of molecular tissue biology185
Enhanced detection of minimal residual disease by targeted sequencing of phased variants in circulating tumor DNA181
Sparse deconvolution improves the resolution of live-cell super-resolution fluorescence microscopy179
Cell segmentation in imaging-based spatial transcriptomics178
Quantitative profiling of pseudouridylation dynamics in native RNAs with nanopore sequencing176
Initialization is critical for preserving global data structure in both t-SNE and UMAP176
Targeted nanopore sequencing by real-time mapping of raw electrical signal with UNCALLED175
Using deep learning to annotate the protein universe174
Targeting a gene regulatory element enhances rice grain yield by decoupling panicle number and size169
Identification of differential RNA modifications from nanopore direct RNA sequencing with xPore168
Efficient CRISPR editing with a hypercompact Cas12f1 and engineered guide RNAs delivered by adeno-associated virus162
m6A RNA modifications are measured at single-base resolution across the mammalian transcriptome158
Identification of mobile genetic elements with geNomad158
MaxDIA enables library-based and library-free data-independent acquisition proteomics157
The expanding vistas of spatial transcriptomics151
Unannotated proteins expand the MHC-I-restricted immunopeptidome in cancer149
Efficient evolution of human antibodies from general protein language models147
Absolute quantification of single-base m6A methylation in the mammalian transcriptome using GLORI147
RNA demethylation increases the yield and biomass of rice and potato plants in field trials145
Single-cell CUT&Tag analysis of chromatin modifications in differentiation and tumor progression143
Treatment of influenza and SARS-CoV-2 infections via mRNA-encoded Cas13a in rodents142
Efficient C•G-to-G•C base editors developed using CRISPRi screens, target-library analysis, and machine learning142
Improved prediction of immune checkpoint blockade efficacy across multiple cancer types142
Precise genomic deletions using paired prime editing138
A knowledge graph to interpret clinical proteomics data137
Evaluating the analytical validity of circulating tumor DNA sequencing assays for precision oncology137
Telomere-to-telomere assembly of diploid chromosomes with Verkko137
CRISPR prime editing with ribonucleoprotein complexes in zebrafish and primary human cells136
Fully phased human genome assembly without parental data using single-cell strand sequencing and long reads136
Generating lineage-resolved, complete metagenome-assembled genomes from complex microbial communities134
A highly photostable and bright green fluorescent protein133
Increasing the throughput of sensitive proteomics by plexDIA132
Population genomic analysis of Aegilops tauschii identifies targets for bread wheat improvement131
Learning protein fitness models from evolutionary and assay-labeled data130
Viral variant-resolved wastewater surveillance of SARS-CoV-2 at national scale129
Hypertension delays viral clearance and exacerbates airway hyperinflammation in patients with COVID-19128
A comprehensive library of human transcription factors for cell fate engineering127
Chromosome-scale, haplotype-resolved assembly of human genomes127
Quantifying the effect of experimental perturbations at single-cell resolution124
Generation of paternal haploids in wheat by genome editing of the centromeric histone CENH3124
A programmable encapsulation system improves delivery of therapeutic bacteria in mice119
Engineering circular RNA for enhanced protein production118
Variability within rare cell states enables multiple paths toward drug resistance118
Quantitative sequencing using BID-seq uncovers abundant pseudouridines in mammalian mRNA at base resolution117
Comprehensive profiling of circular RNAs with nanopore sequencing and CIRI-long117
High-confidence structural annotation of metabolites absent from spectral libraries116
Curated variation benchmarks for challenging medically relevant autosomal genes116
An engineered prime editor with enhanced editing efficiency in plants116
Frequent aneuploidy in primary human T cells after CRISPR–Cas9 cleavage113
Standardized annotation of translated open reading frames113
The Organoid Cell Atlas111
High-throughput total RNA sequencing in single cells using VASA-seq110
Identification of tumor antigens with immunopeptidomics110
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