Many hidden genetic variations can be detected with Chameleolyser, a new method developed in Nijmegen. The information is already yielding new patient diagnoses and may also lead to the discovery of ...
Comparative study of tools for copy number variation detection using next-generation sequencing data
Copy number variation (CNV) plays an important role in disease susceptibility as a type of intermediate-scale structural variation (SV). Accurate CNV detection is crucial for understanding human ...
Total generalized variation models have recently demonstrated high-quality denoising capacity for single image. In this paper, we present an accurate denoising method for depth map. Our method uses a ...
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