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SEQanswers June Challenge Has Begun!

The competition has begun! We're giving away a $50 Amazon gift card to the member who answers the most questions on our site during the month. We want to encourage our community members to share their knowledge and help each other out by answering questions related to sequencing technologies, genomics, and bioinformatics. The competition is open to all members of the site, and the winner will be announced at the beginning of July. Best of luck!

For a list of the official rules, visit (https://www.seqanswers.com/forum/sit...wledge-and-win)
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  • Annovar -filtering

    Hi All,

    I want to use ANNOVAR to run variant reduction, in order to filter out previously identified SNP's in databases such as 1000G, dbSNP, esp6500.
    However I am not really sure of commands to use.

    Also, is there somewhere I can go and read to figure out what other filters to use?

    Could someone please help me out?
    Thank-you!

  • #2
    Here is a description.

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    • #3
      Hi,
      Thank-you for the reply. I looked at the link, that kind of gives an idea of how to pick those SNP's that have been identified already.
      I am looking to do just the opposite.
      Could you point me in the right direction...
      Thank-you!
      Amrita

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