agilent data format
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Weiwei Shi ★ 1.2k
@weiwei-shi-1407
Last seen 10.2 years ago
Dear Listers: This is my first time to look at Agilent's data for one of my research on cross-platform issue; So this is very newbie's question: one example is like this: two files with cy3_50mg_6h_Rat_3125.txt and cy5_50my_6h_Rat_3125.txt. I believe one of them must be control but not sure which one (is there a tradition to use cy5 as control?). One of the dataset's format looks like this: ProbeName GeneName LogRatio PValueLogRatio (+)Pro25G-03 Pro25G -4.92E-01 9.04E-16 (-)3xSLv1 NegativeControl 0.00E+00 1.00E+00 A_43_P21252 CB546590 1.64E-02 7.96E-01 A_42_P534203 272585_Rn -8.69E-03 9.16E-01 A_43_P22195 CB547437 4.77E-02 4.90E-01 A_43_P16421 AA964066 -9.25E-04 9.87E-01 (+)Pro25G-02 Pro25G -1.58E+00 1.10E-33 A_43_P13118 NM_130424 4.12E-02 4.68E-01 A_43_P19445 CB605581 -1.74E-03 9.93E-01 A_43_P11302 BQ206007 -9.17E-02 1.56E-01 A_43_P22361 AA964019 -1.31E-01 5.83E-01 A_43_P10152 BF420136 6.54E-02 4.11E-01 A_42_P573643 234509_Rn 5.87E-02 2.43E-01 I assume the LogRatio is the signal against background? But what is (+)Pro25G-03 or (-)3xSLv1? btw, are there some packages to read this type of data format? Thanks, -- Weiwei Shi, Ph.D Research Scientist GeneGO, Inc. "Did you always know?" "No, I did not. But I believed..." ---Matrix III
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@sean-davis-490
Last seen 3 months ago
United States
Weiwei Shi wrote: > Dear Listers: > > This is my first time to look at Agilent's data for one of my research > on cross-platform issue; So this is very newbie's question: > > one example is like this: > two files with cy3_50mg_6h_Rat_3125.txt and cy5_50my_6h_Rat_3125.txt. > I believe one of them must be control but not sure which one (is there > a tradition to use cy5 as control?). You will almost certainly need to communicate with the biologist that did the arrays to determine the experimental design. > One of the dataset's format looks > like this: > > ProbeName GeneName LogRatio PValueLogRatio > (+)Pro25G-03 Pro25G -4.92E-01 9.04E-16 > (-)3xSLv1 NegativeControl 0.00E+00 1.00E+00 > A_43_P21252 CB546590 1.64E-02 7.96E-01 > A_42_P534203 272585_Rn -8.69E-03 9.16E-01 > A_43_P22195 CB547437 4.77E-02 4.90E-01 > A_43_P16421 AA964066 -9.25E-04 9.87E-01 > (+)Pro25G-02 Pro25G -1.58E+00 1.10E-33 > A_43_P13118 NM_130424 4.12E-02 4.68E-01 > A_43_P19445 CB605581 -1.74E-03 9.93E-01 > A_43_P11302 BQ206007 -9.17E-02 1.56E-01 > A_43_P22361 AA964019 -1.31E-01 5.83E-01 > A_43_P10152 BF420136 6.54E-02 4.11E-01 > A_42_P573643 234509_Rn 5.87E-02 2.43E-01 > > I assume the LogRatio is the signal against background? But what is > (+)Pro25G-03 or (-)3xSLv1? I think the LogRatio is probably the ratio between Red and Green, but there is not a way to tell here. Have these files been manipulated in excel or something? Agilent files typically have a much larger number of columns and have a 9-line header. The (+)Pro25G-03 and (-)3xSLv1 are controls. > btw, are there some packages to read this type of data format? If you have files like the one above, read.table will read them just fine. If you have actual Agilent files (which these are not, I don't think), then the limma package will read them. Sean
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The original paper is not very clear about the data they provided. I am contacting with them about it. If logratio is treat vs. control, why there are two files with similar names which only differ at the dyes' names? I mean both of two files have logratio column but with different number for the same probe. I heard about JMP can handle data preprocessing , normalization , gene selection, multidimensional scaling , PCA , clustering ananysis , and annotation analysis. I am wondering if bioconductor builds a similar pipeline to perform that? This is some work left from others, really making me headache... On 6/14/07, Sean Davis <sdavis2 at="" mail.nih.gov=""> wrote: > Weiwei Shi wrote: > > Dear Listers: > > > > This is my first time to look at Agilent's data for one of my research > > on cross-platform issue; So this is very newbie's question: > > > > one example is like this: > > two files with cy3_50mg_6h_Rat_3125.txt and cy5_50my_6h_Rat_3125.txt. > > I believe one of them must be control but not sure which one (is there > > a tradition to use cy5 as control?). > > You will almost certainly need to communicate with the biologist that > did the arrays to determine the experimental design. > > > One of the dataset's format looks > > like this: > > > > ProbeName GeneName LogRatio PValueLogRatio > > (+)Pro25G-03 Pro25G -4.92E-01 9.04E-16 > > (-)3xSLv1 NegativeControl 0.00E+00 1.00E+00 > > A_43_P21252 CB546590 1.64E-02 7.96E-01 > > A_42_P534203 272585_Rn -8.69E-03 9.16E-01 > > A_43_P22195 CB547437 4.77E-02 4.90E-01 > > A_43_P16421 AA964066 -9.25E-04 9.87E-01 > > (+)Pro25G-02 Pro25G -1.58E+00 1.10E-33 > > A_43_P13118 NM_130424 4.12E-02 4.68E-01 > > A_43_P19445 CB605581 -1.74E-03 9.93E-01 > > A_43_P11302 BQ206007 -9.17E-02 1.56E-01 > > A_43_P22361 AA964019 -1.31E-01 5.83E-01 > > A_43_P10152 BF420136 6.54E-02 4.11E-01 > > A_42_P573643 234509_Rn 5.87E-02 2.43E-01 > > > > I assume the LogRatio is the signal against background? But what is > > (+)Pro25G-03 or (-)3xSLv1? > > I think the LogRatio is probably the ratio between Red and Green, but > there is not a way to tell here. Have these files been manipulated in > excel or something? Agilent files typically have a much larger number > of columns and have a 9-line header. The (+)Pro25G-03 and (-)3xSLv1 are > controls. > > > btw, are there some packages to read this type of data format? > > If you have files like the one above, read.table will read them just > fine. If you have actual Agilent files (which these are not, I don't > think), then the limma package will read them. > > Sean > -- Weiwei Shi, Ph.D Research Scientist GeneGO, Inc. "Did you always know?" "No, I did not. But I believed..." ---Matrix III
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