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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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!
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Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...04-04-2024, 04:25 PM -
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