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Mouratidis, I.

Publications and source records attributed to Mouratidis, I..

18 recordsLinked to original sources

Safeguarding open-weight genomic foundation models through weight locking

BackgroundGenomic foundation models can dramatically accelerate biological research by learning general-purpose representations of genomic data that transfer across tasks, enabling researchers to predict variant effects, regulatory elements, and molecular function, among others. To safeguard against potential biosecurity threats and malicious misuse of open-weight models, a common strategy involves excluding human-infecting viral genomes from the models training corpora. This strategy, however, can be easily circumvented by fine-tuning models on abundantly available viral data. Weight-locking with spectral deformation has been proposed as a potential method to prevent fine-tuning of neural networks, but has not been systematically evaluated in biological AI models. MethodsWe applied spectral deformation locking to the Evo-1-8k-base genomic foundation model and evaluated a panel of attack configurations spanning naive fine-tuning, low-rank adaptation (LoRA), a simple inserted-layer bypass baseline, and a white-box singular value decomposition (SVD)-chain factorisation at chain lengths k [isin] {2, 3, 5}. Recovered virological capability was quantified on three Human Virome Understanding Evaluation (HVUE) tasks. ResultsThe lock defended against the naive attacker by either standard pipeline. Naive full fine-tuning under the strong lock drove downstream virological capability significantly below the pretrained baseline on pathogenicity and host tropism, converting the attack into a capability loss rather than a gain, while naive low-rank adaptation neither moved held-out perplexity (PPL) nor recovered downstream capability above pretrained. Thus, we conclude that by neither route does the naive attacker reach the gain achieved by fine-tuning an unlocked model. Consistent with previous results in non-biological models, an informed attacker who implements the SVD-chain construction does recover capability on pathogenicity prediction, at the cost of increased computational requirements for the fine-tuning process. Availabilityhttps://github.com/Georgakopoulos-Soares-lab/glm-locking.

bioinformatics↗

NYX: Format-aware, learned compression across omics file types

Genomic data repositories continue to grow as sequencing technologies improve, with the NCBI SRA alone exceeding 47 PB. General-purpose compressors treat bioinformatics files as unstructured byte streams and fail to exploit the structured nature of omics data. We present NYX, a format-aware compression system for FASTA, FASTQ, VCF, WIG, H5AD, and BED files. NYX combines lightweight, reversible preprocessing and is build upon the OpenZL framework to take advantage of inherent data structure, delivering high compression ratios while preserving fast and lossless compression. Across representative datasets in the target formats, NYX achieves substantially higher speed than format-specific compressors while maintaining or improving compression ratio.

bioinformatics↗

Fundamental limitations of genomic language models for realistic sequence generation

Large language models (LLMs) have shown remarkable success in natural language processing, prompting interest in their application to genomic sequence analysis. Genomic Language Models (gLMs) based on similar architectures offer a promising avenue for synthetic genome generation and characterization. However, their effectiveness for biological sequence modeling remains poorly characterized. We present a comprehensive evaluation of genomic language models that explicitly aim to generate entire synthetic genomes. We tested Evo 2 on diverse prokaryotic, eukaryotic and viral genomes, and megaDNA on bacteriophage genomes, and assessed performance across key biological features and organizational patterns. Our results reveal systematic failures in gLM-based genomic reconstruction. While the synthetic sequences captured local sequence statistics, they consistently failed to preserve long-range genomic organization, repeat and k-mer composition, transcription factor binding site architecture, and evolutionary constraints. Generated sequences exhibited violations of natural genomic patterns and models showed particular difficulty with repetitive elements. To assess the quality of genome generation, we trained a convolutional neural network that reliably distinguished synthetic from natural sequences, achieving AUROC values up to 0.97 in eukaryotes and 0.82 in prokaryotes, with classification accuracy increasing monotonically with genomic distance from the seed. These findings suggest fundamental limitations in current gLM architectures for capturing the long-range, hierarchical nature of genomic sequences. Our work highlights the need for specialized architectures that explicitly model evolutionary constraints rather than relying solely on statistical patterns, with important implications for computational biology applications requiring realistic sequence generation and for biosafety assessments that depend on the distinguishability of synthetic and natural genomic sequences.

synthetic biology↗

Accelerating Inference in Genomic Foundation Models via Speculative Decoding

Genomic and protein foundation models (GFMs and PFMs) have demonstrated strong performance in learning the language of DNA and proteins, but their use in large-scale sequence generation is limited by the latency of autoregressive decoding. Because every token triggers a forward pass of a large Transformer, whose inference is relatively slow, long-sequence generation quickly becomes costly. In this work we adapt speculative decoding to a representative GFM: the DNA model DNAGPT and two representative PFMs: ProGen2 and ProtGPT2. We implement a probabilistic variant of speculative decoding, in which a lightweight draft model proposes short token spans and a larger target model verifies or corrects them in parallel, while preserving the target models sampling distribution. Across all three models we systematically study the effect of speculation window length, temperature, draft architecture and prompt length, and we benchmark tokens per second over multiple runs per configuration. Speculative decoding yields consistent speedups over standard key-value cached decoding, with maximum observed speedup reaching 100% increase, while average gains across models ranging between 20% and 40% (e.g. 1.2x-1.4x), without changing the underlying target model predictions. Our results show that speculative decoding is a practical and model-agnostic strategy for accelerating genomic and proteomic sequence generation without sacrificing prediction quality.

genomics↗

Quantum implementation of multi-pattern string matching for k-mer detection

MotivationThe exponential growth of publicly available genomic data has created unprecedented opportunities for sequence-based discovery. Locating specific k-mers is fundamental to diverse applications, including metagenomic classification, pathogen and cancer detection, and variant calling yet efficient identification of multiple k-mer patterns across large sequencing data and massive databases remains a significant computational challenge. MethodWe implement two quantum algorithms for DNA multi pattern string matching for k-mer detection based on Grovers amplitude amplification with quantum random access memory (QRAM). The first algorithm uses an enumerate-m oracle that sequentially checks a loaded text substring against all m patterns achieving O({surd}S) query complexity for S text positions but requiring O(m{middle dot}L) work per oracle call. The second algorithm employs nested Grover search with an outer loop over text positions and an inner loop over pattern space, reducing oracle complexity to O(L) while performing O({surd}S {middle dot} {surd}m) in total. ResultsWe present two quantum implementations of multi-pattern string matching tailored for k-mer detection. Leveraging quantum parallelism and Grover-inspired search primitives, our methods accelerate dictionary-based pattern matching, particularly in contexts involving large sequences, such as genomic data, and extensive pattern sets. ConclusionsWhile implementation challenges such as QRAM overhead remain, this study demonstrates both the promise and current limitations of quantum-enhanced string matching, establishing a foundational step toward quantum readiness in bioinformatics. Availability and implementationTo maximize accessibility and practical use, we provide our methodology at: https://github.com/Georgakopoulos-Soares-lab/quantum-multi-motif-finder

bioinformatics↗

The cumulative impact of passenger mutations on cancer development

The traditional binary classification of somatic mutations in cancer as either drivers or passengers overlooks the potential cumulative impact of smaller-effect mutations. Here, we analyze 2,263 whole-genome-sequenced primary tumors across 31 cancer types to assess the functional contribution of passenger mutations in cancer development. We find that in the absence of canonical driver mutations, passenger mutations in cancer genes are significantly enriched, exhibit higher predicted pathogenicity, and are associated with aberrant expression, splicing disruption, altered transcription factor binding, and clinical outcomes that resemble those in the presence of driver mutations. The accumulation of passenger mutations in tumor suppressor genes correlates with significantly reduced expression and poorer prognosis, mirroring the functional outcomes of driver mutations. Notably, this is a previously uncharacterized mechanism of tumor suppressor inactivation, in which the accumulation of somatic mutations results in its progressive inactivation. Our results support a continuum model of mutational impact, where the collective influence of passenger mutations contributes to oncogenesis and clinical outcomes. This work advocates for integrative cancer models that incorporate all somatic mutations to more accurately reflect the complexity of tumor evolution.

cancer biology↗

Landscape and mutational dynamics of G-quadruplexes in the complete human genome and in haplotypes of diverse ancestry

G-quadruplexes (G4s) are alternative DNA structures with diverse biological roles, but their examination in highly repetitive parts of the human genome has been hindered by the lack of reliable sequencing technologies. Recent long-read based genome assemblies have enabled their characterization in previously inaccessible parts of the human genome. Here, we examine the topography and genomic instability of potential G4-forming sequences in the gap-less, reference human genome assembly and in 88 haplotypes of diverse ancestry. We report that G4s are highly enriched in specific repetitive regions, including in certain centromeric and pericentromeric repeat types, and in ribosomal DNA arrays, and experimentally validate the most prevalent G4s detected. G4s tend to have lower methylation than expected throughout the human genome and are genomically unstable, showing an excess of all mutation types, including substitutions, insertions and deletions and most prominently structural variants. Finally, we show that G4s are consistently enriched at PRDM9 binding sites, a protein involved in meiotic recombination. Together, our findings establish G4s as dynamic and functionally significant elements of the human genome and highlight new avenues for investigating their contributions to human disease and evolution.

genomics↗

ZSeeker: An optimized algorithm for Z-DNA detection in genomic sequences

Z-DNA is an alternative left-handed helical form of DNA with a zigzag-shaped backbone that differs from the right-handed canonical B-DNA helix. Z-DNA has been implicated in various biological processes, including transcription, replication, and DNA repair, and can induce genetic instability. Repetitive sequences of alternating purines and pyrimidines have the potential to adopt Z-DNA structures. ZSeeker is a novel computational tool developed for the accurate detection of potential Z-DNA-forming sequences in genomes, addressing limitations of prior methods. By introducing a novel methodology informed and validated by experimental data, ZSeeker enables the refined detection of potential Z-DNA-forming sequences. Built both as a standalone Python package and as an accessible web interface, ZSeeker allows users to input genomic sequences, adjust detection parameters, and view potential Z-DNA sequence distributions and Z-scores via downloadable visualizations. Our Web Platform provides a no-code solution for Z-DNA identification, with a focus on accessibility, user-friendliness, speed and customizability. By providing efficient, high-throughput analysis and enhanced detection accuracy, ZSeeker has the potential to support significant advancements in understanding the roles of Z-DNA in normal cellular functions, genetic instability, and its implications in human diseases. AvailabilityZSeeker is released as a Python package under the GPL license as a multi-platform application and is available at: https://github.com/Georgakopoulos-Soares-lab/ZSeeker. A web-interface of ZSeeker is publicly available at https://zseeker.netlify.app/.

bioinformatics↗

Unraveling diversity by isolating peptide sequences specific to distinct taxonomic groups

The identification of succinct, universal fingerprints that enable the characterization of individual taxonomies can reveal insights into trait development and can have widespread applications in pathogen diagnostics, human healthcare, ecology and the characterization of biomes. Here, we investigated the existence of peptide k-mer sequences that are exclusively present in a specific taxonomy and absent in every other taxonomic level, termed taxonomic quasi-primes. By analyzing proteomes across 24,073 species, we identified quasi-prime peptides specific to superkingdoms, kingdoms, and phyla, uncovering their taxonomic distributions and functional relevance. These peptides exhibit remarkable sequence uniqueness at six- and seven-amino- acid lengths, offering insights into evolutionary divergence and lineage-specific adaptations. Moreover, we show that human quasi-prime loci are more prone to harboring pathogenic variants, underscoring their functional significance. This study introduces taxonomic quasi-primes and offers insights into their contributions to proteomic diversity, evolutionary pathways, and functional adaptations across the tree of life, while emphasizing their potential impact on human health and disease.

bioinformatics↗

invertiaDB: A Database of Inverted Repeats Across Organismal Genomes

Inverted repeats are repetitive elements that can form hairpin and cruciform structures. They are linked to genomic instability, however they also have various biological functions. Their distribution differs markedly across taxonomic groups in the tree of life, and they exhibit high polymorphism due to their inherent genomic instability. Advances in sequencing technologies and declined costs have enabled the generation of an ever-growing number of complete genomes for organisms across taxonomic groups in the tree of life. However, a comprehensive database encompassing inverted repeats across diverse organismal genomes has been lacking. We present InvertiaDB, the first comprehensive database of inverted repeats spanning multiple taxa, featuring repeats identified in the genomes of 118,070 organisms across all major taxonomic groups. The database currently hosts 30,067,666 inverted repeat sequences, serving as a centralized, user-friendly repository to perform searches, interactive visualization, and download existing inverted repeat data for independent analysis. invertiaDB is implemented as a web portal for browsing, analyzing and downloading inverted repeat data. invertiaDB is publicly available at https://invertiadb.netlify.app/homepage.html.

genomics↗

Characterization of hairpin loops and cruciforms across 118,065 genomes spanning the tree of life

Inverted repeats (IRs) can form alternative DNA secondary structures called hairpins and cruciforms, which have a multitude of functional roles and have been associated with genomic instability. However, their prevalence across diverse organismal genomes remains only partially understood. Here, we examine the prevalence of IRs across 118,065 complete organismal genomes. Our comprehensive analysis across taxonomic subdivisions reveals significant differences in the distribution, frequency, and biophysical properties of perfect IRs among these genomes. We identify a total of 29,589,132 perfect IRs and show a highly variable density across different organisms, with strikingly distinct patterns observed in Viruses, Bacteria, Archaea, and Eukaryota. We report IRs with perfect arms of extreme lengths, which can extend to hundreds of thousands of base pairs. Our findings demonstrate a strong correlation between IR density and genome size, revealing that Viruses and Bacteria possess the highest density, whereas Eukaryota and Archaea exhibit the lowest relative to their genome size. Additionally, the study reveals the enrichment of IRs at transcription start and termination end sites in prokaryotes and Viruses and underscores their potential roles in gene regulation and genome organization. Through a comprehensive overview of the distribution and characteristics of IRs in a wide array of organisms, this largest-scale analysis to date sheds light on the functional significance of inverted repeats, their contribution to genomic instability, and their evolutionary impact across the tree of life.

genomics↗

Ribosomal DNA arrays are the most H-DNA rich element in the human genome

Repetitive DNA sequences can form non-canonical structures such as H-DNA which is an intramolecular triplex DNA structure. The new Telomere-to-Telomere (T2T) genome assembly for the human genome has eliminated gaps, enabling the examination of highly repetitive regions including centromeric and pericentromeric repeats and ribosomal DNA arrays. This gapless assembly allows for the examination of the distribution of H-DNA sequences in parts of the human genome that were not previously annotated. We find that H-DNA appears once every 30,000 bps in the human genome. Its distribution is highly inhomogeneous with H-DNA motif hotspots being detectable in acrocentric chromosomes. Ribosomal DNA arrays in acrocentric chromosomes are the genomic element with the highest H-DNA enrichment, with 13.22% of total H-DNA motifs being found in ribosomal DNA arrays, representing a 42.65-fold enrichment over what would be expected by chance. Across the acrocentric chromosomes we report that 55.87% of all H-DNA motifs found in these chromosomes are in rDNA array loci. The H-DNA motifs are primarily found in the intergenic spacer regions of the ribosomal DNA arrays, generating repeated clusters. We also discover that binding sites for PRDM9, a protein that regulates the formation of double-strand breaks and determines the meiotic recombination hotspots in humans and most mammals, are over 5-fold enriched for H-DNA motifs. Finally, we provide evidence that our findings are consistent in other non-human great ape genomes. We conclude that ribosomal DNA arrays are the most enriched genomic loci for H-DNA sequences in human and other great ape genomes.

genomics↗

Quadrupia: Derivation of G-quadruplexes for organismal genomes across the tree of life

G-quadruplex DNA structures exhibit a profound influence on essential biological processes, including transcription, replication, telomere maintenance, and genomic stability. These structures have demonstrably shaped organismal evolution. However, a comprehensive, organism-wide G-quadruplex map encompassing the diversity of life has remained elusive. Here, we introduce Quadrupia, the most extensive and well-characterized G-quadruplex database to date, facilitating the exploration of G-quadruplex structures across the evolutionary spectrum. Quadrupia has identified G-quadruplex sequences in 108,449 reference genomes, with a total of 140,181,277 G-quadruplexes. The database also hosts a collection of 319,784 G-quadruplex clusters of 20 or more members, annotated by taxonomic distributions, multiple sequence alignments, profile Hidden Markov Models and cross-references to G-quadruplex 3D structures. Examination of G-quadruplexes across functional genomic elements in different taxa indicates preferential orientation and positioning, with significant differences between individual taxonomic groups. For example, we find that G-quadruplexes in bacteria with a single replication origin display profound preference for the leading orientation. Finally, we experimentally validate the most frequently observed G-quadruplexes using CD-spectroscopy, UV melting, and fluorescent-based approaches. Quadrupia is publicly available through https://www.pavlopoulos-lab.org/quadrupia.

genomics↗

Nucleic Quasi-Primes: Identification of the Shortest Unique Oligonucleotide Sequences in a Species

Despite the exponential increase in sequencing information driven by massively parallel DNA sequencing technologies, universal and succinct genomic fingerprints for each organism are still missing. Identifying the shortest species-specific nucleic sequences offers insights into species evolution and holds potential practical applications in agriculture, wildlife conservation, and healthcare. We propose a new method for sequence analysis termed nucleic "quasi-primes", the shortest occurring sequences in each of 45,785 organismal reference genomes, present in one genome and absent from every other examined genome. In the human genome, we find that the genomic loci of nucleic quasi-primes are most enriched for genes associated with brain development and cognitive function. In a single-cell case study focusing on the human primary motor cortex, nucleic quasi-prime genes account for a significantly larger proportion of the variation based on average gene expression. Non-neuronal cell-types, including astrocytes, endothelial cells, microglia perivascular-macrophages, oligodendrocytes, and vascular and leptomeningeal cells, exhibited significant activation of quasi-prime containing gene associations related to cancer, while simultaneously suppressing quasi-prime containing genes were associated with cognitive, mental, and developmental disorders. We also show that human disease-causing variants, eQTLs, mQTLs and sQTLs are 4.43-fold, 4.34-fold, 4.29-fold and 4.21-fold enriched at human quasi-prime loci, respectively. These findings indicate that nucleic quasi-primes are genomic loci linked to the evolution of species-specific traits and in humans they provide insights in the development of cognitive traits and human diseases, including neurodevelopmental disorders.

genomics↗

MPRAbase: A Massively Parallel Reporter Assay Database

Massively parallel reporter assays (MPRAs) represent a set of high-throughput technologies that measure the functional effects of thousands of sequences/variants on gene regulatory activity. There are several different variations of MPRA technology and they are used for numerous applications, including regulatory element discovery, variant effect measurement, saturation mutagenesis, synthetic regulatory element generation or characterization of evolutionary gene regulatory differences. Despite their many designs and uses, there is no comprehensive database that incorporates the results of these experiments. To address this, we developed MPRAbase, a manually curated database that currently harbors 129 experiments, encompassing 17,718,677 elements tested across 35 cell types and 4 organisms. The MPRAbase web interface (http://www.mprabase.com) serves as a centralized user-friendly repository to download existing MPRA data for independent analysis and is designed with the ability to allow researchers to share their published data for rapid dissemination to the community.

genomics↗

kmerDB: A Database Encompassing the Set of Genomic and Proteomic Sequence Information for Each Species

The rapid decline in sequencing cost has enabled the generation of reference genomes and proteomes for a growing number of organisms. However, at the present time, there is no established repository that provides information about organism-specific genomic and proteomic sequences of certain lengths, also known as kmers, that are either present or absent in each genome or proteome. In this article, we present kmerDB, a database accessible through an interactive web interface that provides kmer based information from genomic and proteomic sequences in a systematic way. kmerDB currently contains 202,340,859,107 base pairs and 19,304,903,356 amino acids, spanning 45,785 and 22,386 reference genomes and proteomes, respectively, as well as 14,658,776 and 149,264,442 genomic and proteomic species-specific sequences, termed quasi-primes. Additionally, we provide access to 5,186,757 nucleic and 214,904,089 peptide sequences that are absent from every genome and proteome, termed primes. kmerDB features a user-friendly interface offering various search options and filters for easy parsing and searching. The service is available at: www.kmerdb.com.

genomics↗

The determinants of the rarity of nucleic and peptide short sequences in nature

The prevalence of nucleic and peptide short sequences across organismal genomes and proteomes has not been thoroughly investigated. Here we examined 45,785 reference genomes and 21,871 reference proteomes, spanning archaea, bacteria, viruses and eukaryotes to calculate the rarity of short sequences in them. To capture this, we developed a metric of the rarity of each sequence in nature, the Anti-Kardashian index. We find that the frequency of certain dipeptides in rare oligopeptide sequences is hundreds of times lower than expected, which is not the case for any dinucleotides. We also generate predictive regression models that infer the rarity of nucleic and proteomic sequences in nature. For six-mer peptide kmers the R2 performance of the regression models based on amino acid and dipeptide content is 0.816, whereas models based on physicochemical features achieve an R2 of 0.788. For twelve-mer nucleic kmers the R2 performance of our models based on mono and dinucleotides is 0.481. Our results indicate that the mono and dinucleotide composition of nucleic sequences and the amino acids, dipeptides and physicochemical properties of peptide sequences can explain a significant proportion of the variance in their frequencies between organisms in nature.

genomics↗

Absent from DNA and protein: genomic characterization of nullomers and nullpeptides across functional categories and evolution

Nullomers and nullpeptides are short DNA or amino acid sequences that are absent from a genome or proteome, respectively. One potential cause for their absence could be that they have a detrimental impact on an organism. Here, we identified all possible nullomers and nullpeptides in the genomes and proteomes of over thirty species and show that a significant proportion of these sequences are under negative selection. We assign nullomers to different functional categories (coding sequences, exons, introns, 5UTR, 3UTR and promoters) and show that nullomers from coding sequences and promoters are most likely to be selected against. Utilizing variants in the human population, we annotate variant-associated nullomers, highlighting their potential use as DNA fingerprints. Phylogenetic analyses of nullomers and nullpeptides across evolution shows that they could be used to build phylogenetic trees. Our work provides a catalog of genomic and proteome derived absent k-mers, together with a novel scoring function to determine their potential functional importance. In addition, it shows how these unique sequences could be used as DNA fingerprints or for phylogenetic analyses.

genomics↗