Nawar Dalila
@nawardalila.bsky.social
Specialist / Consultant @Rigshospitalet, Copenhagen, Denmark.
NGS data analysis | Genetic Epidemiology | ML/AI
NGS data analysis | Genetic Epidemiology | ML/AI
## Annotate your CNV reports easier with this tool ##
Are you frustrated by the challenges of annotating Copy Number Variation (CNV) reports? Accurate CNV interpretation is crucial in genomic research and clinical diagnostics, yet the process can be complex and time-consuming.
Check this project.
Are you frustrated by the challenges of annotating Copy Number Variation (CNV) reports? Accurate CNV interpretation is crucial in genomic research and clinical diagnostics, yet the process can be complex and time-consuming.
Check this project.
GitHub - nawar82/CNV_liftover_gvf: liftover CNV VCF files from hg38 to 37, extract their data and convert them to GVF files to be imported into third party software for further annotation
liftover CNV VCF files from hg38 to 37, extract their data and convert them to GVF files to be imported into third party software for further annotation - nawar82/CNV_liftover_gvf
github.com
March 13, 2025 at 9:17 PM
## Annotate your CNV reports easier with this tool ##
Are you frustrated by the challenges of annotating Copy Number Variation (CNV) reports? Accurate CNV interpretation is crucial in genomic research and clinical diagnostics, yet the process can be complex and time-consuming.
Check this project.
Are you frustrated by the challenges of annotating Copy Number Variation (CNV) reports? Accurate CNV interpretation is crucial in genomic research and clinical diagnostics, yet the process can be complex and time-consuming.
Check this project.
