Deep SNP: An End-to-end Deep Neural Network with Attention-based Localization for Break-point Detection in SNP Array Genomic data
Hamid Eghbal-zadeh, Lukas Fischer, Niko Popitsch, Florian Kromp,, Sabine Taschner-Mandl, Khaled Koutini, Teresa Gerber, Eva Bozsaky, Peter F., Ambros, Inge M. Ambros, Gerhard Widmer, Bernhard A. Moser

TL;DR
Deep SNP is a novel deep neural network that effectively detects genomic breakpoints in SNP array data, outperforming existing models and potentially enabling more accurate cancer diagnosis and genomic analysis.
Contribution
We introduce Deep SNP, an end-to-end deep learning model with attention-based localization for improved breakpoint detection in genomic data.
Findings
Deep SNP outperforms existing neural network models in breakpoint prediction.
The model successfully predicts breakpoints in large genomic windows.
Qualitative analysis suggests potential for segment prediction without explicit breakpoint coordinates.
Abstract
Diagnosis and risk stratification of cancer and many other diseases require the detection of genomic breakpoints as a prerequisite of calling copy number alterations (CNA). This, however, is still challenging and requires time-consuming manual curation. As deep-learning methods outperformed classical state-of-the-art algorithms in various domains and have also been successfully applied to life science problems including medicine and biology, we here propose Deep SNP, a novel Deep Neural Network to learn from genomic data. Specifically, we used a manually curated dataset from 12 genomic single nucleotide polymorphism array (SNPa) profiles as truth-set and aimed at predicting the presence or absence of genomic breakpoints, an indicator of structural chromosomal variations, in windows of 40,000 probes. We compare our results with well-known neural network models as well as Rawcopy though…
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