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...
Elmentve itt :
Szerzők: |
Ochieng Peter Juma Maróti Zoltán Dombi József Krész Miklós Békési József Kalmár Tibor |
---|---|
Dokumentumtípus: | Cikk |
Megjelent: |
2023
|
Sorozat: | INFORMATION (BASEL)
14 No. 2 |
Tárgyszavak: | |
doi: | 10.3390/info14020128 |
mtmt: | 33643183 |
Online Access: | http://publicatio.bibl.u-szeged.hu/26850 |
Hasonló tételek
-
Adaptive Savitzky-Golay filtering and its applications
Szerző: Dombi József, et al.
Megjelent: (2020) -
Adaptive Multi-round Smoothing Based on the Savitzky-Golay Filter
Szerző: Dombi József, et al.
Megjelent: (2016) -
Evaluation of whole exome sequencing as an alternative to BeadChip and whole genome sequencing in human population genetic analysis
Szerző: Maróti Zoltán, et al.
Megjelent: (2018) -
Whole-Exome Sequencing Identified Two Novel Pathogenic Mutations in the PTCH1 Gene in BCNS
Szerző: Pál Margit, et al.
Megjelent: (2023) -
High-coverage whole-exome sequencing identifies candidate genes for suicide in victims with major depressive disorder
Szerző: Tombácz Dóra, et al.
Megjelent: (2017)