Impact Factor
3.90
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
4.74
1,177 total citations
h5-index
43
h5 depth signal
Cited share
78.7%
218 of 277
Total citations
1,177
Citation footprint
Metric signal
4.70
External metric anchor
Self-citation
2.0%
24 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
United States
318
Germany
125
France
93
China
76
United Kingdom
60
Citing Fields of Research
Genetics & Genomics
775
AI & Machine Learning
116
Noncoding RNA
114
Nucleic Acids Chemistry
105
Bacteriology
67
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
992
Articles tracked across the journal lifetime
Indexed publication set
277
218 cited publications
Last 12 months
195
32.5 publications/month
Open access share
98.5%
192 OA publications in the last year
Leading citing country
United States
318 citing publications
Leading citing field
Genetics & Genomics
775 citing publications
Latest tracked publication
28 September 2026
10 recent records available
Coverage & Indexing History
v6n1, Mar. 2024-
v1n1, Apr. 2019-
Active Coverage
Research Focus & Classification
Indexed Subjects
Genetics & Genomics
Broad Categories
Biochemistry
Genetics
Genetics & Genomics
MeSH Descriptors
Computational Biology
Genomics
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1093/nargab/lqag125
Open DOI
Representation and detection of inversions in pangenome graphs
Pangenome graphs are increasingly used in genetic diversity analyses because they reduce reference bias in read mapping and enhance variant discovery and genotyping from SNPs to structural variants. In pangenome graphs, variants appear a...
02
DOI 10.1093/nargab/lqag115
Open DOI
UniProt data pruning and the growing invisibility of the dark proteome
The protein resource UniProtKB has undergone a major, multi-stage reorganization of its protein space, implemented from release 2025_04 through release 2026_02. Analysis of UniProtKB and UniParc records accessed on 20 January 2026 showed...
03
DOI 10.1093/nargab/lqag118
Open DOI
Pan-cancer multi-omics analysis reveals upregulation of the POLE2 subunit of DNA polymerase epsilon and its associations with patient survival and cellular pathways beyond DNA replication
DNA polymerase epsilon (Polε) is essential for high-fidelity leading-strand synthesis. It comprises a catalytic subunit, POLE, and three accessory subunits, including POLE2. In contrast to POLE, the biological functions and clinical sign...
04
DOI 10.1093/nargab/lqag120
Open DOI
Data-Driven Virus Discovery with Virushunter and Virusgatherer
We present Virushunter and Virusgatherer, a bipartite computational workflow for discovering viral genomes from unprocessed next-generation sequencing data. Virushunter conducts a profile Hidden Markov Model-based sequence homology searc...
05
DOI 10.1093/nargab/lqag119
Open DOI
Controlling for DNA dosage with whole-genome sequencing improves ATAC-seq peak calling
ATAC-seq is a powerful method for mapping chromatin accessibility and identifying cis-regulatory elements (CREs) across cell types. We reveal that ATAC-seq peak calling is compromised by local biases in DNA dosage, arising from copy numb...
06
DOI 10.1093/nargab/lqag121
Open DOI
Correction to ‘Identification and analysis of consensus RNA motifs binding to the genome regulator CTCF’
07
DOI 10.1093/nargab/lqag114
Open DOI
Detect de novo expressed ORFs in transcriptomes with DESwoMAN
De novo gene emergence refers to the process by which new genes arise from mutations in previously non-coding genomic regions. Investigating early stages of de novo gene emergence is essential for understanding the mechanisms that enable...
08
DOI 10.1093/nargab/lqag117
Open DOI
Nanopore sequencing combined with adaptive sampling and NanoExpansion enables accurate characterization of repeat expansion disorders
Expansion repeat disorders are caused by abnormal expansions of short tandem repeats (STRs). We evaluated targeted long-read nanopore sequencing for comprehensive characterization of STR expansions in 132 participants, including patients...
09
DOI 10.1093/nargab/lqag116
Open DOI
Integrating network medicine and foundation models reveals cell-type-specific regulatory alterations in Alzheimer’s disease
Alzheimer’s disease is a complex neurodegenerative disorder characterized by progressive cognitive decline and neuroinflammation. Although its molecular hallmarks are well documented, cell-type-specific mechanisms driving gene dysregulat...
10
DOI 10.1093/nargab/lqag113
Open DOI
Automated GenePy gene-burden computation via a reproducible Nextflow workflow integrated with the Genomics England (GEL) Lifebit platform
Interpretation of rare-disease genomes remains constrained by variant-centric analytical frameworks that insufficiently capture the cumulative impact of multiple variants within a gene. GenePy provides an individual-level, gene-based bur...
Bibliographical & Catalog Notes
Related publication to: Nucleic acids research.
Complemented by (work): Nucleic acids research 0305-1048 (DLC) 74641038 (OCoLC)1791693 (DNLM)0411011.