Pseudogenes variants
Hello How do you behave with pseudogene variants, when you find them in Whole Exome Sequencing, Whole Genome Sequencing or even in sanger sequencing? pleased to hear your expreiences...
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shiyang_bio •
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MiladAD •
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MiladAD •
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Usually I just regard them in the same way as other variants. They are "true" variants. But as these variants might not be functional, so I may discard them when I interpret the result or write an article.
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