ANNOVAR: Revision history

Diff selection: Mark the radio buttons of the revisions to compare and hit enter or the button at the bottom.
Legend: (cur) = difference with latest revision, (prev) = difference with preceding revision, m = minor edit.

21 May 2024

  • curprev 09:2809:28, 21 May 2024‎ Ai talk contribs‎ 6,997 bytes +6,997‎ Created page with "== Overview == ANNOVAR is a software tool used for the annotation of genetic variants detected in diverse genomes. It is widely utilized in the field of bioinformatics to interpret the functional consequences of genetic variants, facilitating the understanding of their potential impact on health and disease. ANNOVAR stands for "ANNOtate VARiation," and it is designed to handle high-throughput sequencing data, providing comprehensive annotations for single nucleo..."
Retrieved from "https://canonica.ai/page/ANNOVAR"