creating a qPCRset from Fluidigm 96*96 arrays in HTqPCR
1
0
Entering edit mode
Norm Allaire ▴ 50
@norm-allaire-6420
Last seen 10.2 years ago
Hi, I'm new to R. I'm trying to analyze 8 Fluidgm 96 *96 plates (96 assays and 192 samples replicated 4 times). I downloaded and installed HTqPCR and I'm now trying to read in the raw data. I am using the "HTqPCR -high-throughput qPCR analysis in R and Bioconductor" April 14, 2011 as a guide but the example in section 13 is for 48*48 arrays. I tried to modify the 48*48 example to make it work with my files but it doesn't seem to work, I get the following error: > temp <- readCtData(exFiles, path = exPath, n.features = 96 * 96, flag = 9, feature =5, type = 6, Ct =7, position= 1, skip 12, sep=",") Error: unexpected numeric constant in "temp <- readCtData(exFiles, path = exPath, n.features = 96 * 96, flag = 9, feature =5, type = 6, Ct =7, position= 1, skip 12" Any thoughts or suggestions would be greatly appreciated! Norm Allaire Scientist II Genetics and Genomics Biogen Idec 14 Cambridge Center Cambridge, MA 02142 Office: 617-679-2932 e-mail: norm.allaire@biogenidec.com<mailto:norm.allaire@biogenidec.com> [[alternative HTML version deleted]]
qPCR qPCR • 1.7k views
ADD COMMENT
0
Entering edit mode
@kipper-fletez-brant-6421
Last seen 6.7 years ago
United States
Hi Norm, Try re-running your code as follows: temp <- readCtData(exFiles, path = exPath, n.features = 96 * 96, flag = 9, feature =5, type = 6, Ct =7, position= 1, skip=12, sep=",") You didn't have an '=' between skip and 12, so R didn't know how to process your input. Best, Kipper Fletez-Brant On Tue, Feb 25, 2014 at 11:58 AM, Norm Allaire <norm.allaire@biogenidec.com>wrote: > Hi, > > I'm new to R. I'm trying to analyze 8 Fluidgm 96 *96 plates (96 assays and > 192 samples replicated 4 times). I downloaded and installed HTqPCR and I'm > now trying to read in the raw data. I am using the "HTqPCR -high- throughput > qPCR analysis in R and Bioconductor" April 14, 2011 as a guide but the > example in section 13 is for 48*48 arrays. I tried to modify the 48*48 > example to make it work with my files but it doesn't seem to work, I get > the following error: > > > temp <- readCtData(exFiles, path = exPath, n.features = 96 * 96, flag = > 9, feature =5, type = 6, Ct =7, position= 1, skip 12, sep=",") > Error: unexpected numeric constant in "temp <- readCtData(exFiles, path = > exPath, n.features = 96 * 96, flag = 9, feature =5, type = 6, Ct =7, > position= 1, skip 12" > > Any thoughts or suggestions would be greatly appreciated! > > > Norm Allaire > Scientist II > Genetics and Genomics > Biogen Idec > 14 Cambridge Center > Cambridge, MA 02142 > Office: 617-679-2932 > e-mail: norm.allaire@biogenidec.com<mailto:norm.allaire@biogenidec.com> > > [[alternative HTML version deleted]] > > _______________________________________________ > Bioconductor mailing list > Bioconductor@r-project.org > https://stat.ethz.ch/mailman/listinfo/bioconductor > Search the archives: > http://news.gmane.org/gmane.science.biology.informatics.conductor > [[alternative HTML version deleted]]
ADD COMMENT
0
Entering edit mode
Hi Kipper, Thanks so much, that worked perfectly! Norm From: Kipper Fletez-Brant [mailto:cafletezbrant@gmail.com] Sent: Tuesday, February 25, 2014 12:05 PM To: Norm Allaire Cc: bioconductor@r-project.org Subject: Re: [BioC] creating a qPCRset from Fluidigm 96*96 arrays in HTqPCR Hi Norm, Try re-running your code as follows: temp <- readCtData(exFiles, path = exPath, n.features = 96 * 96, flag = 9, feature =5, type = 6, Ct =7, position= 1, skip=12, sep=",") You didn't have an '=' between skip and 12, so R didn't know how to process your input. Best, Kipper Fletez-Brant On Tue, Feb 25, 2014 at 11:58 AM, Norm Allaire <norm.allaire@biogenidec.com<mailto:norm.allaire@biogenidec.com>> wrote: Hi, I'm new to R. I'm trying to analyze 8 Fluidgm 96 *96 plates (96 assays and 192 samples replicated 4 times). I downloaded and installed HTqPCR and I'm now trying to read in the raw data. I am using the "HTqPCR -high-throughput qPCR analysis in R and Bioconductor" April 14, 2011 as a guide but the example in section 13 is for 48*48 arrays. I tried to modify the 48*48 example to make it work with my files but it doesn't seem to work, I get the following error: > temp <- readCtData(exFiles, path = exPath, n.features = 96 * 96, flag = 9, feature =5, type = 6, Ct =7, position= 1, skip 12, sep=",") Error: unexpected numeric constant in "temp <- readCtData(exFiles, path = exPath, n.features = 96 * 96, flag = 9, feature =5, type = 6, Ct =7, position= 1, skip 12" Any thoughts or suggestions would be greatly appreciated! Norm Allaire Scientist II Genetics and Genomics Biogen Idec 14 Cambridge Center Cambridge, MA 02142 Office: 617-679-2932 e-mail: norm.allaire@biogenidec.com<mailto:norm.allaire@biogenidec.co m=""><mailto:norm.allaire@biogenidec.com<mailto:norm.allaire@biogenidec.c om="">> [[alternative HTML version deleted]] _______________________________________________ Bioconductor mailing list Bioconductor@r-project.org<mailto:bioconductor@r-project.org> https://stat.ethz.ch/mailman/listinfo/bioconductor Search the archives: http://news.gmane.org/gmane.science.biology.informatics.conductor [[alternative HTML version deleted]]
ADD REPLY

Login before adding your answer.

Traffic: 610 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