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| Main Authors: | , , |
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| Format: | Preprint |
| Published: |
2020
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| Subjects: | |
| Online Access: | https://arxiv.org/abs/2010.03420 |
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Table of Contents:
- Genomic data I used in many fields but, it has become known that most of the platforms used in the sequencing process produce significant errors. This means that the analysis and inferences generated from these data may have some errors that need to be corrected. On the two main types of genome errors - substitution and indels - our work is focused on correcting indels. A deep learning approach was used to correct the errors in sequencing the chosen dataset