## User: Sandro Morganella

Reputation:
30
Status:
New User
Location:
United Kingdom
Last seen:
2 years, 4 months ago
Joined:
3 years, 2 months ago
Email:
m************@gmail.com

#### Posts by Sandro Morganella

<prev • 8 results • page 1 of 1 • next >
1
42
views
1
... How I said it is quite hard for me to understand where the problem is without looking at the data. Anyway, If you could send me the data for chr1 (both cnv and probe data) I will try to understand how to fix the issue. Please use this email morganellaalx [at] gmail.com On Wed, Aug 15, 2018 at 11:05 ...
written 2 days ago by Sandro Morganella30
1
42
views
1
... As last attempt, could you try to run the analysis only on the probes/cnv of chromosome 1? On Mon, Aug 13, 2018 at 8:38 PM, rina [bioc] <noreply@bioconductor.org> wrote: > Activity on a post you are following on support.bioconductor.org > > User rina <https: support.bioconductor. ...
written 5 days ago by Sandro Morganella30
1
42
views
1
... Are the positions of the probes in your markers matrix consistent with the cnv matrix? It is quite hard for me to understand what is the problem without looking at data. On Mon, Aug 13, 2018 at 2:17 PM, rina [bioc] <noreply@bioconductor.org> wrote: > Activity on a post you are following ...
written 5 days ago by Sandro Morganella30
1
42
views
1
... Hi, I think the issue can be related to the order of your matrix. Try to order your matrix so that the sample name is in the first column. In particular your matrix should have exactly this format: $Sample.Name$ Chromosome $Start$ End. $Num.of.Markers$ Aberration The function that loads the ...
written 5 days ago by Sandro Morganella30
1
51
views
1
... No problem, I'm glad it works now. On Thu, Aug 9, 2018 at 9:34 PM, Talip Zengin [bioc] < noreply@bioconductor.org> wrote: > Activity on a post you are following on support.bioconductor.org > > User Talip Zengin <https: support.bioconductor.org="" u="" 14290=""/> wrote Comment: ...
written 9 days ago by Sandro Morganella30
1
51
views
1
... Hi Talip, The probe positions must be sorted by their genomic position. Sorting the probes will fix your problem. Best, Sandro On Thu, Aug 9, 2018 at 3:23 PM, Talip Zengin [bioc] < noreply@bioconductor.org> wrote: > Activity on a post you are following on support.bioconductor.org > > ...
written 9 days ago by Sandro Morganella30
1
244
views
1
... In order to use gaia on this dataset you need to increase R memory limit. Here some useful information: https://stat.ethz.ch/R-manual/R-devel/library/base/html/Memory-limits.html On Fri, Dec 1, 2017 at 1:20 PM, drusmanbashir [bioc] < noreply@bioconductor.org> wrote: > Activity on a pos ...
written 8 months ago by Sandro Morganella30
1
244
views
1
... Hi, From your log I can deduce that it is actually a problem related to the memory. In order to double check this, you can try to run GAIA on a subset of your data (i.e., reduce either the number of probes or the number of samples). Best, Sandro On Fri, Dec 1, 2017 at 12:43 PM, drusmanbashir [b ...
written 8 months ago by Sandro Morganella30

#### Latest awards to Sandro Morganella

No awards yet. Soon to come :-)

Content
Help
Access

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