Briefings in Functional Genomics

Papers
(The median citation count of Briefings in Functional Genomics is 3. 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 2022-01-01 to 2026-01-01.)
ArticleCitations
Experimental and computational methods for studying the dynamics of RNA–RNA interactions in SARS-COV2 genomes59
Single-cell transcriptomics refuels the exploration of spiralian biology57
Role of gut-microbiota in disease severity and clinical outcomes55
Environmental community transcriptomics: strategies and struggles44
Single-cell RNA-seq data clustering by deep information fusion34
Improving cell type identification with Gaussian noise-augmented single-cell RNA-seq contrastive learning30
Comprehensive omics studies of p53 mutants in human cancer26
Genetic variation mining of the Chinese mitten crab (Eriocheir sinensis) based on transcriptome data from public databases25
Deep learning-based classifier of diffuse large B-cell lymphoma cell-of-origin with clinical outcome23
Herbgenomics meets Papaveraceae: a promising -omics perspective on medicinal plant research22
Revisiting hematopoiesis: applications of the bulk and single-cell transcriptomics dissecting transcriptional heterogeneity in hematopoietic stem cells22
Prediction of strand-specific and cell-type-specific G-quadruplexes based on high-resolution CUT&Tag data21
Genome-wide Mendelian randomization and single-cell RNA sequencing analyses identify the causal effects of COVID-19 on 41 cytokines21
Network-medicine approach for the identification of genetic association of parathyroid adenoma with cardiovascular disease and type-2 diabetes19
A lossless reference-free sequence compression algorithm leveraging grammatical, statistical, and substitution rules19
Beyond the hype: using AI, big data, wearable devices, and the internet of things for high-throughput livestock phenotyping17
Functional genomics of ageing: implications of chromatin landscape and beyond16
Advances in integrating single-cell sequencing data to unravel the mechanism of ferroptosis in cancer15
Genomic islands and their role in fitness traits of two key sepsis-causing bacterial pathogens14
Use of in silico approaches, synthesis and profiling of Pan-filovirus GP-1,2 preprotein specific antibodies14
Mapping of long stretches of highly conserved sequences in over 6 million SARS-CoV-2 genomes13
STAT3-dependent long non-coding RNA Lncenc1 contributes to mouse ES cells pluripotency via stabilizing Klf4 mRNA13
Systematic benchmark of single-cell hashtag demultiplexing approaches reveals robust performance of a clustering-based method13
Predicting drug synergy using a network propagation inspired machine learning framework12
DeepPRMS: advanced deep learning model to predict protein arginine methylation sites12
DeepMEns: an ensemble model for predicting sgRNA on-target activity based on multiple features12
Recent advances in differential expression analysis for single-cell RNA-seq and spatially resolved transcriptomic studies12
Expanding interactome analyses beyond model eukaryotes12
A comprehensive survey of dimensionality reduction and clustering methods for single-cell and spatial transcriptomics data11
Interpretation of SNP combination effects on schizophrenia etiology based on stepwise deep learning with multi-precision data11
Be-1DCNN: a neural network model for chromatin loop prediction based on bagging ensemble learning11
amplysis: an R package for microbial composition and diversity analysis using 16S rRNA amplicon data10
Multi-omics studies in interpreting the evolving standard model for immune functions10
Correction to: Machine learning applications on intratumoral heterogeneity in glioblastoma using single-cell RNA sequencing data10
Unmeasured human transcription factor ChIP-seq data shape functional genomics and demand strategic prioritization9
ncRNALocate-EL: a multi-label ncRNA subcellular locality prediction model based on ensemble learning8
A systematic evaluation of the computational tools for ligand-receptor-based cell–cell interaction inference8
SARS-CoV-2 ORF8 dimerization and binding mode analysis with class I MHC: computational approaches to identify COVID-19 inhibitors8
A comprehensive survey on deep learning-based identification and predicting the interaction mechanism of long non-coding RNAs8
Single-cell sequencing: expansion, integration and translation8
Genomic insights into bacteriophages: a new frontier in AMR detection and phage therapy8
NTpred: a robust and precise machine learning framework for in silico identification of Tyrosine nitration sites in protein sequences8
m6A RNA modification pathway: orchestrating fibrotic mechanisms across multiple organs8
Spiralian genomics and the evolution of animal genome architecture8
Integration of single cell multiomics data by deep transfer hypergraph neural network7
The frontier of precision medicine: application of single-cell multi-omics in preimplantation genetic diagnosis7
Pregnancy-specific glycoproteins as potential drug targets for female lung adenocarcinoma patients7
Advancements in genetic techniques and functional genomics for enhancing crop traits and agricultural sustainability7
A comprehensive review of machine learning techniques for multi-omics data integration: challenges and applications in precision oncology7
Correction to: Omics-based deep learning approaches for lung cancer decision-making and therapeutics development7
Attention-based GCN integrates multi-omics data for breast cancer subtype classification and patient-specific gene marker identification7
DeepWalk-aware graph attention networks with CNN for circRNA–drug sensitivity association identification7
Less is more: relative rank is more informative than absolute abundance for compositional NGS data7
Multi-omics therapeutic perspective on ACVR1 gene: from genetic alterations to potential targeting7
A survey on protein–DNA-binding sites in computational biology7
An integrated complete-genome sequencing and systems biology approach to predict antimicrobial resistance genes in the virulent bacterial strains of Moraxella catarrhalis7
Identifying magnetosome-associated genes in the extended CtrA regulon inMagnetospirillum magneticumAMB-1 using a combinational approach6
High-level RNA editing diversifies the coleoid cephalopod brain proteome6
Emerging trends in functional genomics in Spiralia6
MiRNA–gene network embedding for predicting cancer driver genes6
Molecular insights on the origin and development of waxy genotypes in major crop plants5
Comparison of scRNA-seq data analysis method combinations5
From bench to bedside: potential of translational research in COVID-19 and beyond5
Integrating single-cell RNA sequencing data to genome-wide association analysis data identifies significant cell types in influenza A virus infection and COVID-195
Targeting novel sites in DNA gyrase for development of anti-microbials5
Cell type and gene regulatory network approaches in the evolution of spiralian biomineralisation5
iEnhancer-SKNN: a stacking ensemble learning-based method for enhancer identification and classification using sequence information5
Short-homology-mediated PCR-based method for gene introduction in the fission yeast Schizosaccharomyces pombe5
Promoter–motif extraction from co-regulated genes and their relevance to co-expression usingE. colias a model5
RBPLight: a computational tool for discovery of plant-specific RNA-binding proteins using light gradient boosting machine and ensemble of evolutionary features5
COPPER: an ensemble deep-learning approach for identifying exclusive virus-derived small interfering RNAs in plants5
A comprehensive review of approaches for spatial domain recognition of spatial transcriptomes5
A comprehensive protein design protocol to identify resistance mutations and signatures of adaptation in pathogens5
A survey of biclustering and clustering methods in clustering different types of single-cell RNA sequencing data5
pyRforest : a comprehensive R package for genomic data analysis featuring scikit-learn Random Forests in R4
Detecting early-warning signals for influenza by dysregulated dynamic network biomarkers4
Digital PCR and its applications in noninvasive prenatal testing4
SCMcluster: a high-precision cell clustering algorithm integrating marker gene set with single-cell RNA sequencing data4
Molecular language models: RNNs or transformer?4
Multiomics technologies: role in disease biomarker discoveries and therapeutics4
Discoveries by the genome profiling, symbolic powers of non-next generation sequencing methods4
Subtyping and grading of lower-grade gliomas using integrated feature selection and support vector machine4
Computational approaches for direct cell reprogramming: from the bulk omics era to the single cell era4
Breast cancer prognosis through the use of multi-modal classifiers: current state of the art and the way forward4
miRNome-transcriptome analysis unveils the key regulatory pathways involved in the tumorigenesis of tongue squamous cell carcinoma4
Dynamic cancer drivers: a causal approach for cancer driver discovery based on bio-pathological trajectories4
Using artificial intelligence and statistics for managing peritoneal metastases from gastrointestinal cancers4
Single-cell multi-omics sequencing and its application in tumor heterogeneity4
Correction to: STAT3-dependent long non-coding RNA Lncenc1 contributes to mouse ES cells pluripotency via stabilizing Klf4 mRNA4
Gene regulatory network inference based on novel ensemble method3
SAMP: Identifying antimicrobial peptides by an ensemble learning model based on proportionalized split amino acid composition3
Integrating multi-omics data to analyze the potential pathogenic mechanism of CTSH gene involved in type 1 diabetes in the exocrine pancreas3
Significance of understanding the genomics of host–pathogen interaction in limiting antibiotic resistance development: lessons from COVID-19 pandemic3
Exploring the impact of N4-acetylcytidine modification in RNA on non-neoplastic disease: unveiling its role in pathogenesis and therapeutic opportunities3
Characterization of double-stranded RNA and its silencing efficiency for insects using hybrid deep-learning framework3
Long-read RNA sequencing can probe organelle genome pervasive transcription3
Application of computational algorithms for single-cell RNA-seq and ATAC-seq in neurodegenerative diseases3
iEnhancer-DLRA: identification of enhancers and their strengths by a self-attention fusion strategy for local and global features3
An overview of key online resources for human genomics: a powerful and open toolbox for in silico research3
Advancing disease genomics beyond COVID-19 and reducing health disparities: what does the future hold for Africa?3
AAFL: automatic association feature learning for gene signature identification of cancer subtypes in single-cell RNA-seq data3
Identification of deleterious variants of uncertain significance in BRCA2 BRC4 repeat through molecular dynamics simulations3
Genomics in Clinical trials for Breast Cancer3
INTS7 modulates cell proliferation and apoptosis via promoting cell cycle progression in lung adenocarcinoma3
Crosstalk between genomic variants and DNA methylation in FLT3 mutant acute myeloid leukemia3
Multifactorial feature extraction and site prognosis model for protein methylation data3
Widespread transcriptomic alterations of transient receptor potential channel genes in cancer3
Systematic analysis and characterization of long non-coding RNA genes in inflammatory bowel disease3
Multi-omics integration analysis reveals the role of N6-methyladenosine in lncRNA translation during glioma stem cell differentiation3
DeepCMI: a graph-based model for accurate prediction of circRNA–miRNA interactions with multiple information3
Microscale marvels: unveiling the macroscopic significance of micropeptides in human health3
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