Nature Biotechnology

Papers
(The TQCC of Nature Biotechnology is 22. 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 2020-05-01 to 2024-05-01.)
ArticleCitations
PICRUSt2 for prediction of metagenome functions2676
Visualizing and interpreting cancer genomics data via the Xena platform2035
Generalizing RNA velocity to transient cell states through dynamical modeling1463
Genome editing with CRISPR–Cas nucleases, base editors, transposases and prime editors1299
A SARS-CoV-2 surrogate virus neutralization test based on antibody-mediated blockage of ACE2–spike protein–protein interaction1008
SignalP 6.0 predicts all five types of signal peptides using protein language models945
COVID-19 severity correlates with airway epithelium–immune cell interactions identified by single-cell analysis865
Measurement of SARS-CoV-2 RNA in wastewater tracks community infection dynamics758
A unified catalog of 204,938 reference genomes from the human gut microbiome618
Highly sensitive spatial transcriptomics at near-cellular resolution with Slide-seqV2585
CheckV assesses the quality and completeness of metagenome-assembled viral genomes566
Nanopore sequencing technology, bioinformatics and applications559
Multiplex digital spatial profiling of proteins and RNA in fixed tissue525
A lipidome atlas in MS-DIAL 4445
A genomic catalog of Earth’s microbiomes444
Single-cell RNA counting at allele and isoform resolution using Smart-seq3397
Robust decomposition of cell type mixtures in spatial transcriptomics379
Cell2location maps fine-grained cell types in spatial transcriptomics365
Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes341
Spatial transcriptomics at subspot resolution with BayesSpace331
Systematic classification of unknown metabolites using high-resolution fragmentation mass spectra329
CRISPR C-to-G base editors for inducing targeted DNA transversions in human cells325
Delineating copy number and clonal substructure in human tumors from single-cell transcriptomes323
Whole-cell segmentation of tissue images with human-level performance using large-scale data annotation and deep learning308
Fast and accurate protein structure search with Foldseek303
Engineered pegRNAs improve prime editing efficiency299
Wearable materials with embedded synthetic biology sensors for biomolecule detection290
Glycosylase base editors enable C-to-A and C-to-G base changes277
A GRF–GIF chimeric protein improves the regeneration efficiency of transgenic plants271
The clinical progress of mRNA vaccines and immunotherapies269
Improved metagenome binning and assembly using deep variational autoencoders261
Modular, efficient and constant-memory single-cell RNA-seq preprocessing258
A long-term study of AAV gene therapy in dogs with hemophilia A identifies clonal expansions of transduced liver cells248
Differential abundance testing on single-cell data using k-nearest neighbor graphs246
Large language models generate functional protein sequences across diverse families245
Scalable, multimodal profiling of chromatin accessibility, gene expression and protein levels in single cells243
inStrain profiles population microdiversity from metagenomic data and sensitively detects shared microbial strains243
Mapping single-cell data to reference atlases by transfer learning237
Single-cell CUT&Tag profiles histone modifications and transcription factors in complex tissues232
A robust benchmark for detection of germline large deletions and insertions230
Programmable deletion, replacement, integration and inversion of large DNA sequences with twin prime editing226
Cell-free biosensors for rapid detection of water contaminants221
Computational principles and challenges in single-cell data integration220
Tracking COVID-19 with wastewater220
Pre-activated antiviral innate immunity in the upper airways controls early SARS-CoV-2 infection in children219
A Python library for probabilistic analysis of single-cell omics data218
Generation of human striatal organoids and cortico-striatal assembloids from human pluripotent stem cells214
Evaluation of SARS-CoV-2 serology assays reveals a range of test performance207
Carbon-negative production of acetone and isopropanol by gas fermentation at industrial pilot scale205
Readfish enables targeted nanopore sequencing of gigabase-sized genomes204
In vivo adenine base editing of PCSK9 in macaques reduces LDL cholesterol levels201
High-efficiency prime editing with optimized, paired pegRNAs in plants191
Human heart-forming organoids recapitulate early heart and foregut development185
Single-cell metabolic profiling of human cytotoxic T cells180
Ultra-fast proteomics with Scanning SWATH179
Long-term wireless streaming of neural recordings for circuit discovery and adaptive stimulation in individuals with Parkinson’s disease178
CRISPR RNA-guided integrases for high-efficiency, multiplexed bacterial genome engineering177
Fully implantable and bioresorbable cardiac pacemakers without leads or batteries177
Programmable m6A modification of cellular RNAs with a Cas13-directed methyltransferase176
Deep Visual Proteomics defines single-cell identity and heterogeneity169
Predicting the efficiency of prime editing guide RNAs in human cells169
Dual base editor catalyzes both cytosine and adenine base conversions in human cells167
Deep diversification of an AAV capsid protein by machine learning167
A dual-deaminase CRISPR base editor enables concurrent adenine and cytosine editing167
High-plex imaging of RNA and proteins at subcellular resolution in fixed tissue by spatial molecular imaging165
Multi-omics single-cell data integration and regulatory inference with graph-linked embedding165
Mitochondrial copper depletion suppresses triple-negative breast cancer in mice164
Extending and improving metagenomic taxonomic profiling with uncharacterized species using MetaPhlAn 4163
Identification of antimicrobial peptides from the human gut microbiome using deep learning160
Detection of SARS-CoV-2 in nasal swabs using MALDI-MS159
The delivery challenge: fulfilling the promise of therapeutic genome editing159
Dictionary learning for integrative, multimodal and scalable single-cell analysis158
Reimagining high-throughput profiling of reactive cysteines for cell-based screening of large electrophile libraries157
Integration of spatial and single-cell transcriptomic data elucidates mouse organogenesis156
Targeted nanopore sequencing by real-time mapping of raw electrical signal with UNCALLED156
Enhanced detection of minimal residual disease by targeted sequencing of phased variants in circulating tumor DNA155
Integrative analysis of multimodal mass spectrometry data in MZmine 3155
Single-sequence protein structure prediction using a language model and deep learning153
Massively parallel single-cell mitochondrial DNA genotyping and chromatin profiling152
CHANGE-seq reveals genetic and epigenetic effects on CRISPR–Cas9 genome-wide activity152
Sparse deconvolution improves the resolution of live-cell super-resolution fluorescence microscopy151
Spatial components of molecular tissue biology148
Haplotype-resolved assembly of diploid genomes without parental data146
Quantitative profiling of pseudouridylation dynamics in native RNAs with nanopore sequencing146
Initialization is critical for preserving global data structure in both t-SNE and UMAP145
Functional, metabolic and transcriptional maturation of human pancreatic islets derived from stem cells143
Using deep learning to annotate the protein universe140
A male-biased sex-distorter gene drive for the human malaria vector Anopheles gambiae139
High-dose AAV gene therapy deaths137
Prediction of the sequence-specific cleavage activity of Cas9 variants137
Identification of differential RNA modifications from nanopore direct RNA sequencing with xPore137
Base editors for simultaneous introduction of C-to-T and A-to-G mutations136
Deep brain optogenetics without intracranial surgery136
Identifying phenotype-associated subpopulations by integrating bulk and single-cell sequencing data135
Spatially informed cell-type deconvolution for spatial transcriptomics134
Unannotated proteins expand the MHC-I-restricted immunopeptidome in cancer127
Efficient CRISPR editing with a hypercompact Cas12f1 and engineered guide RNAs delivered by adeno-associated virus125
Single-cell CUT&Tag analysis of chromatin modifications in differentiation and tumor progression124
Treatment of influenza and SARS-CoV-2 infections via mRNA-encoded Cas13a in rodents123
Fully phased human genome assembly without parental data using single-cell strand sequencing and long reads123
Targeted, efficient sequence insertion and replacement in rice122
Drag-and-drop genome insertion of large sequences without double-strand DNA cleavage using CRISPR-directed integrases121
Cell segmentation in imaging-based spatial transcriptomics121
Unlocking the promise of mRNA therapeutics120
Evaluating the analytical validity of circulating tumor DNA sequencing assays for precision oncology120
Hypertension delays viral clearance and exacerbates airway hyperinflammation in patients with COVID-19119
Efficient C•G-to-G•C base editors developed using CRISPRi screens, target-library analysis, and machine learning119
m6A RNA modifications are measured at single-base resolution across the mammalian transcriptome119
MaxDIA enables library-based and library-free data-independent acquisition proteomics118
Efficient gene editing of human long-term hematopoietic stem cells validated by clonal tracking118
Targeting a gene regulatory element enhances rice grain yield by decoupling panicle number and size115
Modeling neural tube development by differentiation of human embryonic stem cells in a microfluidic WNT gradient112
Precise genomic deletions using paired prime editing111
A comprehensive library of human transcription factors for cell fate engineering110
Improved prediction of immune checkpoint blockade efficacy across multiple cancer types110
Chromosome-scale, haplotype-resolved assembly of human genomes109
Wireless, closed-loop, smart bandage with integrated sensors and stimulators for advanced wound care and accelerated healing109
CRISPR prime editing with ribonucleoprotein complexes in zebrafish and primary human cells108
Generating lineage-resolved, complete metagenome-assembled genomes from complex microbial communities108
RNA demethylation increases the yield and biomass of rice and potato plants in field trials107
Generation of paternal haploids in wheat by genome editing of the centromeric histone CENH3107
Biopharmaceutical benchmarks 2022107
A genome resource for green millet Setaria viridis enables discovery of agronomically valuable loci106
A knowledge graph to interpret clinical proteomics data104
Comprehensive profiling of circular RNAs with nanopore sequencing and CIRI-long103
Population genomic analysis of Aegilops tauschii identifies targets for bread wheat improvement101
Implications of antibody-dependent enhancement of infection for SARS-CoV-2 countermeasures100
High-confidence structural annotation of metabolites absent from spectral libraries100
Cell type prioritization in single-cell data100
Optimization of AsCas12a for combinatorial genetic screens in human cells100
Variability within rare cell states enables multiple paths toward drug resistance99
Rapid image deconvolution and multiview fusion for optical microscopy99
Quantifying the effect of experimental perturbations at single-cell resolution98
Identification of tumor antigens with immunopeptidomics97
Engineering luminescent biosensors for point-of-care SARS-CoV-2 antibody detection96
COVID-19 antibodies on trial96
The Organoid Cell Atlas96
A five-transgene cassette confers broad-spectrum resistance to a fungal rust pathogen in wheat96
Increasing the throughput of sensitive proteomics by plexDIA95
Learning protein fitness models from evolutionary and assay-labeled data94
The expanding vistas of spatial transcriptomics92
Targeting herpes simplex virus with CRISPR–Cas9 cures herpetic stromal keratitis in mice91
Standardized annotation of translated open reading frames91
Absolute quantification of single-base m6A methylation in the mammalian transcriptome using GLORI91
Deletion and replacement of long genomic sequences using prime editing91
Imaging volumetric dynamics at high speed in mouse and zebrafish brain with confocal light field microscopy91
A programmable encapsulation system improves delivery of therapeutic bacteria in mice91
Characterizing allele- and haplotype-specific copy numbers in single cells with CHISEL91
An engineered prime editor with enhanced editing efficiency in plants90
Saturation variant interpretation using CRISPR prime editing90
An engineered ScCas9 with broad PAM range and high specificity and activity89
Curated variation benchmarks for challenging medically relevant autosomal genes88
A near-infrared genetically encoded calcium indicator for in vivo imaging88
Expanding RNAi therapeutics to extrahepatic tissues with lipophilic conjugates87
Viral variant-resolved wastewater surveillance of SARS-CoV-2 at national scale87
Compact RNA editors with small Cas13 proteins86
DestVI identifies continuums of cell types in spatial transcriptomics data85
A dual-constriction biological nanopore resolves homonucleotide sequences with high fidelity85
Noncanonical open reading frames encode functional proteins essential for cancer cell survival84
Telomere-to-telomere assembly of diploid chromosomes with Verkko84
CRISPR-free base editors with enhanced activity and expanded targeting scope in mitochondrial and nuclear DNA84
The PROTAC gold rush84
Engineering circular RNA for enhanced protein production81
Massively parallel kinetic profiling of natural and engineered CRISPR nucleases81
Genome-wide specificity of prime editors in plants80
Frequent aneuploidy in primary human T cells after CRISPR–Cas9 cleavage80
Auto-deconvolution and molecular networking of gas chromatography–mass spectrometry data80
Single-cell immunology of SARS-CoV-2 infection80
GABA-enriched tomato is first CRISPR-edited food to enter market79
ChIP-seq of plasma cell-free nucleosomes identifies gene expression programs of the cells of origin79
Integrated analysis of plasma and single immune cells uncovers metabolic changes in individuals with COVID-1979
High-yield genome engineering in primary cells using a hybrid ssDNA repair template and small-molecule cocktails78
Super-resolution RNA imaging using a rhodamine-binding aptamer with fast exchange kinetics78
A split prime editor with untethered reverse transcriptase and circular RNA template78
Monitoring deep-tissue oxygenation with a millimeter-scale ultrasonic implant78
Benchmarking of T cell receptor repertoire profiling methods reveals large systematic biases78
Efficient evolution of human antibodies from general protein language models77
Gene signature extraction and cell identity recognition at the single-cell level with Cell-ID76
Send in the senolytics76
Multiscale and integrative single-cell Hi-C analysis with Higashi76
Sequence-specific prediction of the efficiencies of adenine and cytosine base editors76
Cholesterol-functionalized DNA/RNA heteroduplexes cross the blood–brain barrier and knock down genes in the rodent CNS75
Assessing single-cell transcriptomic variability through density-preserving data visualization75
Spatial charting of single-cell transcriptomes in tissues75
A fluorescent sensor for spatiotemporally resolved imaging of endocannabinoid dynamics in vivo75
The RNA Atlas expands the catalog of human non-coding RNAs75
scJoint integrates atlas-scale single-cell RNA-seq and ATAC-seq data with transfer learning74
A highly photostable and bright green fluorescent protein73
Overcoming barriers to early disease intervention73
Remote smartphone monitoring of Parkinson’s disease and individual response to therapy73
High-throughput total RNA sequencing in single cells using VASA-seq72
Directed remodeling of the mouse gut microbiome inhibits the development of atherosclerosis71
Determination of isoform-specific RNA structure with nanopore long reads71
Efficient in vitro and in vivo RNA editing via recruitment of endogenous ADARs using circular guide RNAs71
Extending the small-molecule similarity principle to all levels of biology with the Chemical Checker70
Chromatin Velocity reveals epigenetic dynamics by single-cell profiling of heterochromatin and euchromatin70
High-fidelity Cas13 variants for targeted RNA degradation with minimal collateral effects70
Bioinstructive implantable scaffolds for rapid in vivo manufacture and release of CAR-T cells70
Engineered off-the-shelf therapeutic T cells resist host immune rejection70
Quantitative sequencing using BID-seq uncovers abundant pseudouridines in mammalian mRNA at base resolution70
Transplantation of a human liver following 3 days of ex situ normothermic preservation70
Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study69
Prediction of drug efficacy from transcriptional profiles with deep learning69
Heritable transgene-free genome editing in plants by grafting of wild-type shoots to transgenic donor rootstocks69
Automated design of thousands of nonrepetitive parts for engineering stable genetic systems67
The COVID-19 XPRIZE and the need for scalable, fast, and widespread testing67
A humanized mouse model of chronic COVID-1966
Inferring gene expression from cell-free DNA fragmentation profiles66
Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing66
Integrating T cell receptor sequences and transcriptional profiles by clonotype neighbor graph analysis (CoNGA)66
Plug-and-play control of a brain–computer interface through neural map stabilization66
Genome-scale metabolic reconstruction of 7,302 human microorganisms for personalized medicine65
Identification of highly selective covalent inhibitors by phage display65
Oral delivery of systemic monoclonal antibodies, peptides and small molecules using gastric auto-injectors65
Programmable A-to-Y base editing by fusing an adenine base editor with an N-methylpurine DNA glycosylase64
Engineered circular ADAR-recruiting RNAs increase the efficiency and fidelity of RNA editing in vitro and in vivo64
A comprehensive SARS-CoV-2–human protein–protein interactome reveals COVID-19 pathobiology and potential host therapeutic targets64
High-throughput mapping of a whole rhesus monkey brain at micrometer resolution63
Could mutations of SARS-CoV-2 suppress diagnostic detection?62
Rationalized deep learning super-resolution microscopy for sustained live imaging of rapid subcellular processes62
Single-cell measurement of higher-order 3D genome organization with scSPRITE62
Isolating live cell clones from barcoded populations using CRISPRa-inducible reporters61
Modular cytokine receptor-targeting chimeras for targeted degradation of cell surface and extracellular proteins60
A multicenter study benchmarking single-cell RNA sequencing technologies using reference samples60
Animal-free alternatives and the antibody iceberg60
Combinatorial design of nanoparticles for pulmonary mRNA delivery and genome editing60
Context-aware dimensionality reduction deconvolutes gut microbial community dynamics59
Nanopore sequencing of single-cell transcriptomes with scCOLOR-seq59
Super-resolved spatial transcriptomics by deep data fusion59
Uncovering the mode of action of engineered T cells in patient cancer organoids58
Functional single-cell genomics of human cytomegalovirus infection58
A unified haplotype-based method for accurate and comprehensive variant calling57
A small and highly sensitive red/far-red optogenetic switch for applications in mammals57
A network analysis of COVID-19 mRNA vaccine patents56
Systematic discovery of recombinases for efficient integration of large DNA sequences into the human genome56
A tissue-engineered uterus supports live births in rabbits56
Artificial intelligence, drug repurposing and peer review56
Identification of mobile genetic elements with geNomad56
Evolution of an adenine base editor into a small, efficient cytosine base editor with low off-target activity56
Transcriptome-wide profiling and quantification of N6-methyladenosine by enzyme-assisted adenosine deamination56
Re-engineering the adenine deaminase TadA-8e for efficient and specific CRISPR-based cytosine base editing55
Modeling intercellular communication in tissues using spatial graphs of cells55
Single-nuclei isoform RNA sequencing unlocks barcoded exon connectivity in frozen brain tissue55
The scverse project provides a computational ecosystem for single-cell omics data analysis55
Epineural optogenetic activation of nociceptors initiates and amplifies inflammation55
Base editing sensor libraries for high-throughput engineering and functional analysis of cancer-associated single nucleotide variants55
Wireless closed-loop optogenetics across the entire dorsoventral spinal cord in mice53
A genome and gene catalog of glacier microbiomes53
Smartphone apps in the COVID-19 pandemic52
Iterative single-cell multi-omic integration using online learning52
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