Impact Factor
2.31
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
1.14
75 total citations
h5-index
12
h5 depth signal
Cited share
46.4%
32 of 69
Total citations
75
Citation footprint
Metric signal
0.67
External metric anchor
Self-citation
2.7%
2 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
China
170
United States
84
Russia
55
India
52
Iran
25
Citing Fields of Research
Genetics & Genomics
264
AI & Machine Learning
146
Protein Structure & Folding
130
Nucleic Acids Chemistry
44
Evolutionary Genomics
38
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
1,350
Articles tracked across the journal lifetime
Indexed publication set
69
32 cited publications
Last 12 months
29
4.8 publications/month
Open access share
0.0%
0 OA publications in the last year
Leading citing country
China
170 citing publications
Leading citing field
Genetics & Genomics
264 citing publications
Latest tracked publication
8 October 2026
10 recent records available
Coverage & Indexing History
v1n1, Apr. 2003-
v1n1, Apr. 2003-
Active Coverage
Research Focus & Classification
Indexed Subjects
Genetics & Genomics
AI & Machine Learning
Protein Structure & Folding
Nucleic Acids Chemistry
Mass Spectrometry
Broad Categories
Computational Biology
Genetics & Genomics
Protein Structure & Folding
MeSH Descriptors
Computational Biology
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1142/s0219720026500125
Open DOI
A dual-level sparsity Bayesian framework for rare-variant association analysis using integrated nested laplace approximation
Background. Rare genetic variants (minor allele frequency, MAF <1%) carry a substantial share of the unexplained heritability of complex human traits, yet set-based association tests lose power precisely in the regime in which rare varia...
02
DOI 10.1142/s0219720026500113
Open DOI
ICUDrug: AI-Based Safe Drug Recommendation Model for Sepsis via Time-Windowed and Drug-Drug Interaction Analysias
Sepsis is a type of life-threatening organ dysfunction caused by dysregulated host response to infection. Given the heterogenous nature of sepsis, precise and temporally-optimized drug recommen-dations are critical, yet existing AI-based...
03
DOI 10.1142/s0219720026710046
Open DOI
When current taxids make historical taxa look new
A taxon can keep its biological identity while its numeric identifier changes over time. Reconstructing a past taxonomy state by resolving each sequence to its current-day identifier ignores this and can make an already-existing taxon lo...
04
DOI 10.1142/s0219720026500137
Open DOI
Cell-cycle–interferon coordination changes across proliferative states in TNBC/basal-like breast cancer
Cohort-wide pathway correlations can hide strong relationships that differ across tumor states. We asked whether this occurs in TNBC/basal-like breast cancer by ordering tumors on prespecified Hallmark pathway axes and comparing pathway ...
05
DOI 10.1142/s0219720026500101
Open DOI
Anchors for homology-based scaffolding
Homology-based scaffolding orders contigs based on conserved collinearity of homologous sequences across related species. Existing methods often rely on costly whole-genome alignments or show limited robustness when integrating multiple ...
06
DOI 10.1142/s0219720026500095
Open DOI
A scalable pan-genomic pipeline for annotation-free discovery of species-specific markers: Application to Staphylococcus aureus
Current bioinformatics approaches for bacterial diagnostic target discovery remain constrained by their reliance on gene annotations and fixed-boundary genome segmentation, which overlook unannotated intergenic regions and introduce sequ...
07
DOI 10.1142/s0219720026500083
Open DOI
CNV-ECOD: A copy number variation detection method based on ECOD algorithm using next-generation sequencing data
Copy number variation (CNV), as a major type of DNA structural variations (SVs), plays a key role in causing human diseases and contributing to genetic diversity. Accurate identification of CNVs is significant for disease mechanism analy...
08
DOI 10.1142/s021972002650006x
Open DOI
ReinVar: A model-free paradigm-based reinforcement learning approach to detect copy number variation
Copy number variation (CNV) is one of the most imperative forms of structural variations that can span over the coding and non-coding regulatory regions of an individual’s genome. Copy number variations (CNV) can significantly impact the...
09
DOI 10.1142/s0219720026710034
Open DOI
When pipelines run but coordinates fail: A simple spatial specificity check for false locality in post-GWAS analysis
Some post-GWAS analysis software can run to completion without reporting an error while producing results that are not biologically valid. We call this failure false locality: a result appears to be local to a gene or protein because it ...
10
DOI 10.1142/s0219720026500071
Open DOI
Trap spaces as labelled ideals of SCC posets: A structural–functional theory of reachability in asynchronous boolean networks
Boolean networks provide a qualitative framework for modelling regulatory systems when kinetic parameters are unavailable, with cellular phenotypes represented as attractors of the induced dynamics [J. D. Schwab et al., Concepts in Boole...
Bibliographical & Catalog Notes
Latest issue consulted: Vol. 1, no. 3 (Oct. 2003).
Also issued online.
v. 1, no. 1 (Mar. 2003)20040901 Notice not published Printed on acid-free paper