Genomic Variations Explorer (GenVarX): a toolset for annotating promoter and CNV regions using genotypic and phenotypic differences

The rapid growth of sequencing technology and its increasing popularity in biology-related research over the years has made whole genome re-sequencing (WGRS) data become widely available. A large amount of WGRS data can unlock the knowledge gap between genomics and phenomics through gaining an under...

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Detalles Bibliográficos
Autores principales: Chan, Yen On, Biová, Jana, Mahmood, Anser, Dietz, Nicholas, Bilyeu, Kristin, Škrabišová, Mária, Joshi, Trupti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10623549/
https://www.ncbi.nlm.nih.gov/pubmed/37928239
http://dx.doi.org/10.3389/fgene.2023.1251382

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10623549/
https://www.ncbi.nlm.nih.gov/pubmed/37928239
http://dx.doi.org/10.3389/fgene.2023.1251382

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