Bioinformatics

Bioinformatics

生物信息学

  • 3区 中科院分区
  • Q1 JCR分区

高引用文章

文章名称 引用次数
Minimap2: pairwise alignment for nucleotide sequences 537
ape 5.0: an environment for modern phylogenetics and evolutionary analyses in R 514
fastp: an ultra-fast all-in-one FASTQ preprocessor 513
Nextstrain: real-time tracking of pathogen evolution 193
RAxML-NG: a fast, scalable and user-friendly tool for maximum likelihood phylogenetic inference 192
VarSome: the human genomic variant search engine 156
NanoPack: visualizing and processing long-read sequencing data 146
Benchmarking fold detection by DaliLite v.5 107
DFAST: a flexible prokaryotic genome annotation pipeline for faster genome publication 105
Parallelization of MAFFT for large-scale multiple sequence alignments 100
NGL viewer: web-based molecular graphics for large complexes 85
FROGS: Find, Rapidly, OTUs with Galaxy Solution 79
TISIDB: an integrated repository portal for tumor-immune system interactions 79
MetaboAnalystR: an R package for flexible and reproducible analysis of metabolomics data 77
iFeature: a Python package and web server for features extraction and selection from protein and peptide sequences 76
Predicting miRNA-disease association based on inductive matrix completion 76
Updating the 97% identity threshold for 16S ribosomal RNA OTUs 70
Heavy-tailed prior distributions for sequence count data: removing the noise and preserving large differences 69
Modeling polypharmacy side effects with graph convolutional networks 68
PopLDdecay: a fast and effective tool for linkage disequilibrium decay analysis based on variant call format files 68
iTerm-PseKNC: a sequence-based tool for predicting bacterial transcriptional terminators 68
admetSAR 2.0: web-service for prediction and optimization of chemical ADMET properties 62
Versatile genome assembly evaluation with QUAST-LG 60
Identify origin of replication in Saccharomyces cerevisiae using two-step feature selection technique 57
i6mA-Pred: identifying DNA N-6 - methyladenine sites in the rice genome 57
DincRNA: a comprehensive web-based bioinformatics toolkit for exploring disease associations and ncRNA function 57
The lncLocator: a subcellular localization predictor for long non-coding RNAs based on a stacked ensemble classifier 56
ACPred-FL: a sequence-based predictor using effective feature representation to improve the prediction of anti-cancer peptides 51
Phandango: an interactive viewer for bacterial population genomics 50
deepDR: a network-based deep learning approach to in silico drug repositioning 49
heatmaply: an R package for creating interactive cluster heatmaps for online publishing 48
BNPMDA: Bipartite Network Projection for MiRNA-Disease Association prediction 47
IRscope: an online program to visualize the junction sites of chloroplast genomes 46
iLoc-lncRNA: predict the subcellular location of lncRNAs by incorporating octamer composition into general PseKNC 45
PhenoScanner V2: an expanded tool for searching human genotype-phenotype associations 44
DeepDTA: deep drug-target binding affinity prediction 43
Tumor origin detection with tissue-specific miRNA and DNA methylation markers 43
Efficient comparative phylogenetics on large trees 42
The revival of the Gini importance ? 41
Scaling read aligners to hundreds of threads on general-purpose processors 41
FATHMM-XF: accurate prediction of pathogenic point mutations via extended features 41
iPromoter-2L: a two-layer predictor for identifying promoters and their types by multi-window-based PseKNC 40
SPRING: a kinetic interface for visualizing high dimensional single-cell expression data 40
Comprehensive evaluation of transcriptome-based cell-type quantification methods for immuno-oncology 40
GSCALite: a web server for gene set cancer analysis 39
ARGs-OAP v2.0 with an expanded SARG database and Hidden Markov Models for enhancement characterization and quantification of antibiotic resistance genes in environmental metagenomes 39
Mosdepth: quick coverage calculation for genomes and exomes 38
DIABLO: an integrative approach for identifying key molecular drivers from multi-omics assays 36
A graph regularized non-negative matrix factorization method for identifying microRNA-disease associations 36
SEED 2: a user-friendly platform for amplicon high-throughput sequencing data analyses 36