Entering edit mode
Here are a few of the many applications:
1) variant calling 2) gene expression 3) DNA binding 4) chromatin modification 5) chromosome conformation
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could you please add one or two lines in each of them briefing what they do actually?
Have you tried searching the web? I'm sure you'll find descriptions of each of these applications without much effort.
I could get the concepts easily. But the problem is, I could not relate them with read-reference mapping. Could you please help me to relate them by specifying that exactly where read-reference mapping is needed?
For variant calling, you need to compare your data to a reference to identify sequence differences. For gene expression/DNA binding/chromatin modification, you need to count the number of reads at different genes/target loci. For chromosome conformation, you need to determine which loci are physically interacting. All of these applications require mapping to a reference.
One needs to take into account "support" (depth/number of reads piling up in the region after alignment) for a particular observation when doing any of the things originally listed by @Harold. This requires reference/read maps.