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BMC Bioinformatics

短名	BMC Bioinform.
Journal Impact	2.73
国际分区	MATHEMATICAL & COMPUTATIONAL BIOLOGY(Q1)
期刊索引	SCI Q2中科院 3 区

ISSN	1471-2105
h-index	242
国内分区	生物学(3区)生物学生化研究方法(3区)生物学数学与计算生物学(3区)生物学生物工程与应用微生物(4区)

BMC BIOINFORMATICS 是一本开放获取、同行评议的期刊，考虑关于各种生物数据建模和分析的计算和统计方法的开发、测试和新应用以及计算生物学的其他领域的所有方面的文章.BMC BIOINFORMATICS 是 BMC 系列的一部分，该系列出版特定主题的期刊，重点关注生物学和医学所有领域的个体研究团体的需求。我们提供高效、公平和友好的同行评审服务，并致力于出版所有可靠的科学，前提是工作提供的知识有所进步。

期刊主页投稿网址

涉及主题	生物计算机科学化学遗传学生物化学基因计算生物学人工智能数学数据挖掘程序设计语言基因表达统计机器学习生物信息学物理操作系统DNA微阵列工程类医学哲学
出版信息	出版商: BioMed Central Ltd，出版周期: Monthly，期刊类型: journal
基本数据	创刊年份: 2000，原创研究文献占比: 99.66%，自引率:3.40%， Gold OA占比: 99.64%
平均审稿周期	网友分享经验：平均2.8个月
平均录用比例	网友分享经验：约50%

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专利引用格式

Distinguishing word identity and sequence context in DNA language models

2024-9-13

scBubbletree: computational approach for visualization of single cell RNA-seq data

2024-9-13

A novel approach to the analysis of Overall Survival (OS) as response with Progression-Free Interval (PFI) as condition based on the RNA-seq expression data in The Cancer Genome Atlas (TCGA)

2024-9-13

Mild cognitive impairment prediction based on multi-stream convolutional neural networks

2024-9-12

altAFplotter: a web app for reliable UPD detection in NGS diagnostics

2024-9-12

PopMLvis: a tool for analysis and visualization of population structure using genotype data from genome-wide association studies

2024-9-11

BayesianSSA: a Bayesian statistical model based on structural sensitivity analysis for predicting responses to enzyme perturbations in metabolic networks

2024-9-10

HiCMC: High-Efficiency Contact Matrix Compressor

2024-9-10

Mouse embryo CoCoPUTs: novel murine transcriptomic-weighted usage website featuring multiple strains, tissues, and stages

2024-9-6

Assigning credit where it is due: an information content score to capture the clinical value of multiplexed assays of variant effect

2024-9-6

Cortexa: a comprehensive resource for studying gene expression and alternative splicing in the murine brain

2024-9-5

Inference of single-cell network using mutual information for scRNA-seq data analysis

2024-9-5

Answering open questions in biology using spatial genomics and structured methods

2024-9-4

Variant graph craft (VGC): a comprehensive tool for analyzing genetic variation and identifying disease-causing variants

2024-9-3

VCF observer: a user-friendly software tool for preliminary VCF file analysis and comparison

2024-9-3

Correction: Advancing drug–target interaction prediction: a comprehensive graph-based approach integrating knowledge graph embedding and ProtBert pretraining

2024-9-3

Tensor product algorithms for inference of contact network from epidemiological data

2024-9-2

PCP-GC-LM: single-sequence-based protein contact prediction using dual graph convolutional neural network and convolutional neural network

2024-9-2

SmithHunter: a workflow for the identification of candidate smithRNAs and their targets

2024-9-2

PSSM-Sumo: deep learning based intelligent model for prediction of sumoylation sites using discriminative features

2024-8-30

CNVDeep: deep association of copy number variants with neurocognitive disorders

2024-8-29

Prediction of mutation-induced protein stability changes based on the geometric representations learned by a self-supervised method

2024-8-28

HerpesDRG: a comprehensive resource for human herpesvirus antiviral drug resistance genotyping

2024-8-27

HBeeID: a molecular tool that identifies honey bee subspecies from different geographic populations

2024-8-27

ARGV: 3D genome structure exploration using augmented reality

2024-8-27

Optimizing biomedical information retrieval with a keyword frequency-driven prompt enhancement strategy

2024-8-27

refMLST: reference-based multilocus sequence typing enables universal bacterial typing

2024-8-27

Smccnet 2.0: a comprehensive tool for multi-omics network inference with shiny visualization

2024-8-24

MSH-DTI: multi-graph convolution with self-supervised embedding and heterogeneous aggregation for drug-target interaction prediction

2024-8-23

TIANA: transcription factors cooperativity inference analysis with neural attention

2024-8-22

HPC-T-Annotator: an HPC tool for de novo transcriptome assembly annotation

2024-8-21

Denoiseit: denoising gene expression data using rank based isolation trees

2024-8-21

VAIV bio-discovery service using transformer model and retrieval augmented generation

2024-8-21

Modeling relaxation experiments with a mechanistic model of gene expression

2024-8-20

Benchmarking robustness of deep neural networks in semantic segmentation of fluorescence microscopy images

2024-8-20

Correction: Enhancing SNV identification in whole-genome sequencing data through the incorporation of known genetic variants into the minimap2 index

2024-8-19

GCphase: an SNP phasing method using a graph partition and error correction algorithm

2024-8-19

A comparative analysis of mutual information methods for pairwise relationship detection in metagenomic data

2024-8-14

AFFECT: an R package for accelerated functional failure time model with error-contaminated survival times and applications to gene expression data

2024-8-13

BEROLECMI: a novel prediction method to infer circRNA-miRNA interaction from the role definition of molecular attributes and biological networks

2024-8-10

Occlusion enhanced pan-cancer classification via deep learning

2024-8-8

Maptcha: an efficient parallel workflow for hybrid genome scaffolding

2024-8-8

Adaptive loss-guided multi-stage residual ASPP for lesion segmentation and disease detection in cucumber under complex backgrounds

2024-8-8

Drug repositioning based on residual attention network and free multiscale adversarial training

2024-8-8

RankCompV3: a differential expression analysis algorithm based on relative expression orderings and applications in single-cell RNA transcriptomics

2024-8-7

Correction: Holomics ‑ a user‑friendly R shiny application for multi‑omics data integration and analysis

2024-8-7

scMaui: a widely applicable deep learning framework for single-cell multiomics integration in the presence of batch effects and missing data

2024-8-6

StackedEnC-AOP: prediction of antioxidant proteins using transform evolutionary and sequential features based multi-scale vector with stacked ensemble learning

2024-8-4

Random forests for the analysis of matched case–control studies

2024-8-1

Hybrid fragment-SMILES tokenization for ADMET prediction in drug discovery

2024-8-1

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最新文章

Distinguishing word identity and sequence context in DNA language models

scBubbletree: computational approach for visualization of single cell RNA-seq data

A novel approach to the analysis of Overall Survival (OS) as response with Progression-Free Interval (PFI) as condition based on the RNA-seq expression data in The Cancer Genome Atlas (TCGA)

Mild cognitive impairment prediction based on multi-stream convolutional neural networks

altAFplotter: a web app for reliable UPD detection in NGS diagnostics

PopMLvis: a tool for analysis and visualization of population structure using genotype data from genome-wide association studies

BayesianSSA: a Bayesian statistical model based on structural sensitivity analysis for predicting responses to enzyme perturbations in metabolic networks

HiCMC: High-Efficiency Contact Matrix Compressor

Mouse embryo CoCoPUTs: novel murine transcriptomic-weighted usage website featuring multiple strains, tissues, and stages

Assigning credit where it is due: an information content score to capture the clinical value of multiplexed assays of variant effect

Cortexa: a comprehensive resource for studying gene expression and alternative splicing in the murine brain

Inference of single-cell network using mutual information for scRNA-seq data analysis

Answering open questions in biology using spatial genomics and structured methods

Variant graph craft (VGC): a comprehensive tool for analyzing genetic variation and identifying disease-causing variants

VCF observer: a user-friendly software tool for preliminary VCF file analysis and comparison

Correction: Advancing drug–target interaction prediction: a comprehensive graph-based approach integrating knowledge graph embedding and ProtBert pretraining

Tensor product algorithms for inference of contact network from epidemiological data

PCP-GC-LM: single-sequence-based protein contact prediction using dual graph convolutional neural network and convolutional neural network

SmithHunter: a workflow for the identification of candidate smithRNAs and their targets

PSSM-Sumo: deep learning based intelligent model for prediction of sumoylation sites using discriminative features

CNVDeep: deep association of copy number variants with neurocognitive disorders

Prediction of mutation-induced protein stability changes based on the geometric representations learned by a self-supervised method

HerpesDRG: a comprehensive resource for human herpesvirus antiviral drug resistance genotyping

HBeeID: a molecular tool that identifies honey bee subspecies from different geographic populations

ARGV: 3D genome structure exploration using augmented reality

Optimizing biomedical information retrieval with a keyword frequency-driven prompt enhancement strategy

refMLST: reference-based multilocus sequence typing enables universal bacterial typing

Smccnet 2.0: a comprehensive tool for multi-omics network inference with shiny visualization

MSH-DTI: multi-graph convolution with self-supervised embedding and heterogeneous aggregation for drug-target interaction prediction

TIANA: transcription factors cooperativity inference analysis with neural attention

HPC-T-Annotator: an HPC tool for de novo transcriptome assembly annotation

Denoiseit: denoising gene expression data using rank based isolation trees

VAIV bio-discovery service using transformer model and retrieval augmented generation

Modeling relaxation experiments with a mechanistic model of gene expression

Benchmarking robustness of deep neural networks in semantic segmentation of fluorescence microscopy images

Correction: Enhancing SNV identification in whole-genome sequencing data through the incorporation of known genetic variants into the minimap2 index

GCphase: an SNP phasing method using a graph partition and error correction algorithm

A comparative analysis of mutual information methods for pairwise relationship detection in metagenomic data

AFFECT: an R package for accelerated functional failure time model with error-contaminated survival times and applications to gene expression data

BEROLECMI: a novel prediction method to infer circRNA-miRNA interaction from the role definition of molecular attributes and biological networks

Occlusion enhanced pan-cancer classification via deep learning

Maptcha: an efficient parallel workflow for hybrid genome scaffolding

Adaptive loss-guided multi-stage residual ASPP for lesion segmentation and disease detection in cucumber under complex backgrounds

Drug repositioning based on residual attention network and free multiscale adversarial training

RankCompV3: a differential expression analysis algorithm based on relative expression orderings and applications in single-cell RNA transcriptomics

Correction: Holomics ‑ a user‑friendly R shiny application for multi‑omics data integration and analysis

scMaui: a widely applicable deep learning framework for single-cell multiomics integration in the presence of batch effects and missing data

StackedEnC-AOP: prediction of antioxidant proteins using transform evolutionary and sequential features based multi-scale vector with stacked ensemble learning

Random forests for the analysis of matched case–control studies

Hybrid fragment-SMILES tokenization for ADMET prediction in drug discovery

帮你贴心管理全部的文献.css-5myebc{font-size:14px;font-weight:var(--chakra-fontWeights-normal);margin-top:var(--chakra-space-1);margin-bottom:var(--chakra-space-1);}研飞ivySCI，高效的论文管理

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