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Old 01-11-2012, 04:10 AM   #1
nans_bn
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Default tools to detect copy number variants

Hello,

Could anyone suggest some good and reliable tools to detect SVs (CNVs) for human genome and exome data generated from both SOLiD and Illumina platform ?

Thank you..
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Old 01-12-2012, 03:38 AM   #2
gprakhar
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Hi,

Please take a look at these posts, as this topic has been discussed before.

http://seqanswers.com/forums/showthread.php?t=12361
http://seqanswers.com/forums/showthread.php?t=9480

Regards,
--
pg
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Old 01-12-2012, 04:25 AM   #3
nans_bn
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Thanks a lot.
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