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Old 08-10-2012, 01:49 AM   #2
stefanoberri
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Location: Cambridge area, UK

Join Date: Jan 2010
Posts: 35
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Hi

I am the developer of CNAnorm which is designed for normalisation, segmentation, GC correction and plotting of copy number data from very low coverage (~ 0.05X) whole genome sequencing. It also works with higher coverage (obviously takes more time and you will need a few tweeks) and some report using it sucesfully on exome capture data.

Please read this post where other users posted their questions and I provided some suggestions.

good luck
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