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How Do Researchers Interpret Genomic Data?
Researchers use a variety of bioinformatics tools and databases to interpret genomic data:
1.
Variant Calling
: Identifying genetic variants from sequencing data.
2.
Functional Annotation
: Assigning functions to genetic variants.
3.
Pathway Analysis
: Understanding how genetic alterations affect biological pathways.
4.
Comparative Genomics
: Comparing genomic data from cancer patients with healthy individuals to identify significant differences.
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