refseq

How does RefSeq support Genetic Analysis in Cancer?


RefSeq supports genetic analysis in cancer through its comprehensive collection of annotated sequences. These sequences help in:
Mutation Identification: By comparing sequences from cancer samples to the reference sequences, researchers can identify somatic mutations and germline mutations that may contribute to cancer development.
Gene Expression Studies: RefSeq provides the necessary reference for analyzing gene expression levels in cancer cells versus normal cells, helping to identify oncogenes and tumor suppressor genes.
Pathway Analysis: Understanding the genetic pathways involved in cancer can be facilitated by using RefSeq to map genes and their interactions.

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