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Thread | Thread Starter | Forum | Replies | Last Post |
Patchwork - allele-specific somatic CNAs in cancer (WGS) | mackan | Bioinformatics | 2 | 04-19-2012 05:54 AM |
bioinformatics training for WGS 454 and Illumina | hmmngs | Bioinformatics | 2 | 09-21-2011 09:01 AM |
Recommendation for windows NGS analysis software | Hamid | General | 2 | 05-19-2011 11:00 AM |
Which technology is better for CNV detection, SOLiD or Solexa? | El Mariachi | SOLiD | 0 | 12-30-2010 01:45 AM |
CNV detection via BAM depth-of-coverage | quinlana | Bioinformatics | 4 | 09-10-2010 05:58 AM |
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#1 |
Member
Location: beijing Join Date: Jul 2012
Posts: 33
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Can anyone recommend some reliable software for CNV detection in cancer cells for Illumina WGS data?
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#2 |
Member
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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#3 |
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Location: beijing Join Date: Jul 2012
Posts: 33
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Hi, stefanoberri, I am not able to access the paper for CNAnorm, could you mind to send me the paper in mailbox: hhhyyyccc@gmail.com? I appreciate it !
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#4 |
Member
Location: Cambridge area, UK Join Date: Jan 2010
Posts: 35
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Hi, sorry for the late reply.
Here you can find the preprint of the article and the supplemental material Last edited by stefanoberri; 08-15-2012 at 09:47 AM. |
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#5 |
Member
Location: beijing Join Date: Jul 2012
Posts: 33
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I am not able to open the link, could you send the article to me in : hhhyyyccc@gmail.com
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