Adaptive Savitzky–Golay Filters for Analysis of Copy Number Variation Peaks from Whole-Exome Sequencing Data
Copy number variation (CNV) is a form of structural variation in the human genome that provides medical insight into complex human diseases; while whole-genome sequencing is becoming more affordable, whole-exome sequencing (WES) remains an important tool in clinical diagnostics. Because of its disco...
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| Format: | Article |
| Published: |
2023
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| Series: | INFORMATION (BASEL)
14 No. 2 |
| Subjects: | |
| doi: | 10.3390/info14020128 |
| mtmt: | 33643183 |
| Online Access: | http://publicatio.bibl.u-szeged.hu/26850 |