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DeepSV: Accurate calling of genomic deletions from high-throughput sequencing data using deep convolutional neural network

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Calling genetic variations from sequence reads is an important problem in genomics. There are many existing methods for calling various types of variations. Recently, Google developed a method for calling single nucleotide polymorphisms (SNPs) based on deep learning. Their method visualizes sequence reads in the forms of images.

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Nội dung Text: DeepSV: Accurate calling of genomic deletions from high-throughput sequencing data using deep convolutional neural network

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