CGH segmentation algorithms (snapCGH package)
1
0
Entering edit mode
João Fadista ▴ 500
@joao-fadista-1942
Last seen 10.2 years ago
An embedded and charset-unspecified text was scrubbed... Name: not available Url: https://stat.ethz.ch/pipermail/bioconductor/attachments/20071119/ bf3c8b96/attachment.pl
• 692 views
ADD COMMENT
0
Entering edit mode
Ramon Diaz ★ 1.1k
@ramon-diaz-159
Last seen 10.2 years ago
Dear Joao, I am not sure your idea would get you what you want. The issue you rise has been addressed before in other fields where you want to combine several disgnostics or experts or classifiers. For example, if you search for "mixtures of experts" you'll find a lot of hits. Machine learning textbooks often have one or more chapters devoted to this issue. You might try to derive a (meta-) algorithm that combines the output from those three, based upon some training data (of a structure similar to yours) for which the truth is known. In some cases, using algorithms which return a probability makes combination simpler (i.e., if each algorithm tells you how sure it is of its assessment); that is not really the case with any of the three you mention. Best, R. On Monday 19 November 2007 10:46, Jo?o Fadista wrote: > Dear all, > > I used 3 different segmentation algorithms (DNAcopy, GLAD and HomHMM from > snapCGH package) to assess copy number variation in my data and I want to > have a criteria to choose the best CNVs found. There are cases where all > the 3 algorithms find the same CNV, cases where only 2 algorithms find the > same CNV and cases where only 1 algorithm finds a CNV. > > Somebody could argue that a good criteria should be to exclude CNVs found > with only 1 algorithm but I found that sometimes those CNVs are really > there when I make a visual inspection of the data. I thought about making a > Mann-Whitney test for each CNV to compare the log2-ratios between n probes > from the CNV with (c-n) probes from the control region, where 'c' > represents the total number of probes for that chromosome that are not in > any CNV on that array. After correcting for multiple testing, a p-value is > assign for each CNV giving me a criteria to choose the best CNVs found. > > Any comments on my approach and alternative ones will be very much > appreciated. Thanks in advance. > > > Best regards, > Jo?o Fadista > > [[alternative HTML version deleted]] -- Ram?n D?az-Uriarte Statistical Computing Team Centro Nacional de Investigaciones Oncol?gicas (CNIO) (Spanish National Cancer Center) Melchor Fern?ndez Almagro, 3 28029 Madrid (Spain) Fax: +-34-91-224-6972 Phone: +-34-91-224-6900 http://ligarto.org/rdiaz PGP KeyID: 0xE89B3462 (http://ligarto.org/rdiaz/0xE89B3462.asc) **NOTA DE CONFIDENCIALIDAD** Este correo electr?nico, y ...{{dropped:3}}
ADD COMMENT

Login before adding your answer.

Traffic: 736 users visited in the last hour
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6