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18 months ago
sahalpaladan ▴ 10

What is the criteria used in igv to show the given variant is observed or not?

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to show the given variant is observed or not?

what do you mean ? IGV is not a variant caller , it 'just' displays the bases

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I understand IGV is used to visualize aligned reads. Let me rephrase my query above. I have observed few set of variants in my vcf file, and when I visualize those variants in IGV browser, nucleotide changes with >20% are displayed as false positive, however, if the observed nucleotide change is <=20%, IGV browser sometimes categorizing it as not false positive or sometimes as false positive. I'm not sure on what criteria it's segregating these values. Could you please clarify this?

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Look, we cannot see your screen, not your file. Please show data and screenshots. What in your option is a false positive?

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