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13.1 years ago
Sara
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50
Hi everone,
How can we detect large indels ( more than 25 bp) in exome sequence data?
Any references?
Thanks Sara
Hi everone,
How can we detect large indels ( more than 25 bp) in exome sequence data?
Any references?
Thanks Sara
Have a look at this nice site: http://bioops.info/2011/02/software-packages-for-discovering-structural-variation-with-next-generation-sequencing/
A somewhat unconventional approach, first de novo assembly then align the contigs to detect the indels. The candidates can be verified by read mapping. This would miss some true indels, but I'd expect less false positives.
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Different technologies mean different read lengths which mean different approaches to problem solving.
What sequencing technology? Are you using single or paired-end data?
Noob here in HT sequencing. May I know what the sequencing technology have to do with it?