The acquisition of a genetic alteration dataset is a process allowing researchers to access comprehensive collections of variant information. Such access typically involves obtaining a digital copy of this information for local analysis and study. An instance of this is retrieving a database containing single nucleotide polymorphisms (SNPs) and insertions/deletions (indels) from various populations or individuals.
The availability of these resources facilitates advancements in various fields, including personalized medicine, drug discovery, and population genetics. Historically, the development of high-throughput sequencing technologies has driven the need for efficient methods of obtaining and managing these large datasets. Easy acquisition of these resources empowers researchers to explore the genetic basis of disease, identify potential drug targets, and understand human evolution more effectively.
