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8.7 years ago
bioinforesearchquestions
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370
Dear all,
I am going to analyze whole genome sequence (WGS) data of Human sample. I need some clarifications on following terminologies.
- what is coverage and depth?
- I have seen people use WGS with expected coverage 30X. Why specifically 30X?
- How to see my WGS coverage information?
- Is there any
tools
to detect the coverage information? - Does expected coverage changes for RNAseq and DNASeq?
- What is the relationship between SNP and coverage?
Possible answer for all your questions - What Is The Sequencing 'Depth' ?
Thanks Venu for the link. I will go through the link