Biology subjects

Yilmaz, M. A.

Publications and source records attributed to Yilmaz, M. A..

2 recordsLinked to original sources

bioRxiv2025

CHALLENGER: Detecting Copy Number Variants in Challenging Regions Using Whole Genome Sequencing Data

Copy number variation (CNV) detection remains a major challenge in whole-genome sequencing (WGS) data, particularly within repetitive, duplicated, and camouflaged genomic regions where short-read sequencing (srWGS) often fails to produce confident alignments. Although long-read WGS (lrWGS) substantially improves structural variant resolution, its high cost limits widespread adoption, especially in clinical settings. To address these limitations, we introduce CHALLENGER, a masked language modeling-based approach for clinical CNV detection using short-read depth signals over coding regions. While the model uses only short-read data as input, it can make calls typically accessible only with long reads, providing a cost-effective way to obtain information characteristic of both technologies. The model is pre-trained on semi-ground truth calls made on srWGS data and then fine-tuned using (i) lrWGS-derived, (ii) human expert-labeled, and (iii) experimentally validated CNV call sets, enabling it to learn technology- and labeling strategy-specific variant signatures hidden within srWGS profiles and to operate in challenging genomic regions. We show that our short-read-only approach improves the state-of-the-art CNV detection F1-score by 40.8%, while, for the first time, capturing 80.3% of CNVs that can only be detected using long reads in challenging genomic regions. The improvement in F1-score in the set of human experts calls is 70.5% for duplications, and 24.6% for deletions in challenging genes. We also specialize CHALLENGER on paralog genes SMN1/2, AMY1/2, and NPY4R, and show that it can improve the performance on experimentally validated call sets while being able to make paralog-specific calls in addition to aggregate calls. The CHALLENGER code and model are available at GitHub.

bioinformatics↗

bioRxiv2025

ExactCN: Predicting Exact Copy Numbers on Whole Exome Sequencing Data

The quantification of the precise copy number variations (CNVs) is crucial to understanding the effects of gene dosage, disease severity, and therapeutic response. Although whole-exome sequencing (WES) offers a cost-effective solution for CNV detection in a clinical setting, it introduces several biases, including those related to sequence length, GC content, and the use of targeting probes. Consequently, estimating exact copy numbers remains challenging, especially for WES data. Here, we present ExactCN, a deep learning-based method for estimation of exact copy numbers from WES data per exon. The architecture integrates convolutional layers that extract local read-depth patterns with transformer encoder blocks that capture genomic context and handle sequencing noise. ExactCN is trained on WES samples from the 1000 Genomes Project, using matching WGS-based calls as semi-ground truth. In benchmarks, ExactCN improves the state-of-the-art integer CNV calling performance by reducing the macro-averaged mean absolute error (MAE) from 0.91 to 0.62 and the macro-averaged root mean squared error (RMSE) from 1.31 to 0.78. It also achieves an overall Pearson correlation of 0.669 and Spearman correlation of 0.550, improving the second-best method by 0.641 and 0.482, respectively. Furthermore, a fine-tuned and specialized version of ExactCN for aggregate CNV detection in clinically important duplicated genes SMN1/2 achieved a macro averaged F1-score of 0.657, and mean absolute error of 0.3. These results substantially improves the state-of-the-art performance and demonstrates the models applicability to both research and clinical genomic analyses. ExactCN is available at https://github.com/ciceklab/ExactCN.

bioinformatics↗