Question: (Closed) (Waiting on OP) human genome intronic variants
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Hello rajesh,
Please add why you're working on this - the bigger picture, as well as some detail on what you've tried so far. Please read through our https://www.biostars.org/t/how-to to understand how to ask a question on a scientific forum. Please add details within the next 24 hours, or I will have to close the question as being too vague.
i am working on some genomics projects, for that project i need that kind of dataset which have intronic variants. many thanks.
That's still very vague.
A database of WGS data from a huge number of individuals is gnomAD
Like Wouter said, the statement doesn't clarify much.
What kind of data are you looking for? What do you wish to do with it? What attributes are you looking to extract?
i am looking for insertion, deleltion. substitution, SNV in human genome intronic region. many thanks
Are you looking for (population-specific) frequencies, rs numbers, locations,...
Sorry to ask this, but do you have a clear picture on what you're trying to accomplish? Also, SNVs and substitutions are the same thing.
Hello rajesh !
We believe that this post does not fit the main topic of this site.
Closing until OP clarifies.
For this reason we have closed your question. This allows us to keep the site focused on the topics that the community can help with.
If you disagree please tell us why in a reply below, we'll be happy to talk about it.
Cheers!