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Old 11-08-2017, 06:56 AM   #1
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Location: Kyiv, Ukraine

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Default Detecting indels from visualized read alignments

Dear colleagues,
how can you tell, just by looking at the read alignment in a genome viewer (IGV or Genome Browse), that there is a small indel in a particular region of interest. Usually, it is needed when checking candidate SNPs manually.
I am working with trios.
Thank you
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