bioRxiv Science⌕ Search

bioRxiv · 10.64898/2026.04.06.716730

Germline VCF Annotator: a lightweight pipeline for processing germline VCFs with robust variant extraction and read evidence quality control

Abstract

Raw variant calls are typically distributed as VCF files and are not well-suited for direct human review. They are intended for programmatic parsing, and spreadsheet import can distort data through automatic type conversion. Furthermore, variants in VCF are commonly annotated to add gene context and predicted functional consequences. Ensembl VEP, a widely used standard for transcript-aware variant annotation, was adapted in this study to generate standardized consequence fields across genomic features. Using a colon crypt whole-genome sequencing cohort as the motivating dataset, this study examined whether variation at DNA damage response and repair (DDR) loci could contribute to mutation-burden patterns in normal colon crypts, including patterns associated with age and potential treatment-related exposure. To make this question testable in a reproducible table-based format, the Germline VCF Annotator was developed as a two-step workflow that normalizes germline VCFs, generates VEP tabular annotations with explicit allele fields, and then extracts variants of interest and appends read-evidence metrics to assign a rules-based QC class. Within-patient concordance across technical repeats at predefined DDR loci was near-perfect after filtering for nonsilent SNVs with read depth [≥]15, with discordance concentrated among Low-QC loci. Bulk and crypt-derived samples showed no age-related trend in DDR burden. Although the demonstration centers on DDR and aging, the Germline VCF Annotator is applicable to other gene sets that require human-readable locus-level summaries with retained allele provenance and read evidence.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Manojlovic, Z.. 2026-04-09. Germline VCF Annotator: a lightweight pipeline for processing germline VCFs with robust variant extraction and read evidence quality control. https://doi.org/10.64898/2026.04.06.716730

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

CellChat Hotspot: A Targeted Approach to Cell Cell Communication Analysis With Spatial transcriptomics Validation.

Abstract. In recent years, single cell RNA sequencing (scRNA seq) has enabled the investigation of intercellular communication through Cell Cell Communication (CCC) tools such as CellChat. Despite their potential, these approaches remain challenging to interpret, particularly when global analyses generate complex interaction networks that may include biologically irrelevant signals. To address this limitation, we developed a framework termed CellChat Hotspot, designed to improve the biological interpretability of inferred communication networks. This approach integrates gene set enrichment analysis with a context driven filtering strategy, selecting both genes and cells based on their functional relevance prior to communication inference. Applied to stage II colon cancer data, CellChat Hotspot enabled the identification of condition-specific interaction patterns associated with recurrence. Non recurrent patients showed enrichment of immune related processes, whereas recurrent cases were characterized by pathways associated with invasion and metastasis. Notably, a loss of interaction in the HSPG pathway between CALB1+ and stromal cells was observed in recurrent patients, suggesting a potential disruption of cell matrix adhesion mechanisms. To verify the reliability of this finding, we applied the framework to spatial transcriptomics data, which confirmed the presence of the HSPG2 DAG1 interaction in non-recurrent tumors and its near absence in recurrent ones. Overall, this framework provides a biologically guided strategy for studying intercellular communication in complex systems such as the tumor microenvironment.

bioinformatics↗

SIFT: Syncmer-Informed Selection of Haplotypes for T2T Imputation

Genome patching improves the completeness of fragmented assemblies by filling unresolved gaps with sequences from reference genomes. Pangenome panels provide diverse candidate haplotypes for this task, but identifying suitable references efficiently becomes increasingly challenging as these panels grow. We present SIFT, a compressed indexing method for selecting reference haplotypes for genome patching with ImpuT2T. SIFT combines closed-syncmer parsing, phrase-level indexing, and pseudo-maximal exact match (pseudo-MEM) queries. Closed syncmers provide a context-independent parsing rule with bounded distances between consecutive selected positions, enabling consistent parsing of reference and query sequences. We demonstrate that two closed syncmers determine the distance at which they can occur consecutively in any string, so that equal substrings of two parses represent identical sequences and no gap sequence need be stored. SIFT indexes the reference parse and its reverse using run-length compressed suffix arrays and adapts the Boyer-Moore-Li search procedure to identify pseudo-MEMs between the reference parse and query parse. It then aggregates matching evidence to identify candidate reference haplotypes for downstream patching. This framework connects compressed sequence indexing with haplotype selection and provides a basis for querying large reference panels at the phrase level. SIFT is publicly available under the GNU license at https://github.com/EddieFerro/SIFT.

bioinformatics↗

Assessing the Capacity of Genomic Language Models to Generate Informative Embeddings of Viral Genome Fragments

Genomic language models (gLMs) trained on large volumes of nucleotide sequences are becoming an alternative to classical methods in metagenomic analysis, particularly for studying genomic "dark matter". In this work, we investigate the ability of four gLMs (DNABERT-2, DNABERT-S, ViraLM, and Evo2-7B) to generate taxonomically informative vector representations of short viral genome fragments. We constructed a balanced reference dataset of viruses based on the ICTV Virus Metadata Resource and compared the representations generated by gLMs with conventional k-mer profiles and MinHash sketches using clustering and neighborhood-based metrics (adjusted Rand index (ARI), precision@k, and CROSS precision@k). On the reference dataset, three of the four gLMs outperformed the 4-mer profile in terms of ARI and precision@5 under the same evaluation protocol. The best performance was generally achieved by intermediate model layers. Conventional k-mer profiles consistently outperformed MinHash sketches. We further evaluated the methods on two viral orders (egoviruses and mriyaviruses) absent from the reference dataset, with model layers and k-mer lengths selected exclusively on the reference dataset. DNABERT-S showed the most consistently strong performance across these two orders, ranking first on mriyaviruses and second on egoviruses, while k-mer profiles with Jensen-Shannon distance remained competitive. We also observed the consistency of representations between forward fragments and their reverse complements. Overall, the best-performing gLMs surpassed conventional baselines, although their advantage depended on the dataset and evaluation metric. The consistently strong performance of DNABERT-S suggests a potential benefit of contrastive fine-tuning and indicates that larger models are not necessarily more effective for generating taxonomically informative representations.

bioinformatics↗