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Hi,
Our sequence analysis provider sent us a xlsx file instead of vcf formatted file with SNPs and InDels. Is there a workaround to use this in IGV in order to visualize these variations against reference genome?
I included the screenshot of column alignment.
Thank you,
Venura
Helga Thorvaldsdottir
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Jul 6, 2018, 1:58:24 PM7/6/18
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