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Hello, I have this command: x.axis <- seq(from=0.5, to=4.5, length.out=13112) How can I which of the x.axis components is the closest to a given value, for example 3.2? Best, Dani -- Daniel Valverde Saub? Grup de Biologia Molecular de Llevats Facultat de Veterin?ria de la Universitat Aut?noma de Barcelona Edifici V, Campus UAB 08193 Cerdanyola del Vall?s- SPAIN Centro de Investigaci?n Biom?dica en Red en Bioingenier?a, Biomateriales y Nanomedicina (CIBER-BBN) Grup d'Aplicacions Biom?diques de la RMN Facultat de Bioci?ncies Universitat Aut?...

...like to know how to put this expression to the y axis ?mol/10^6 cells I've tried some combinations using the expression() function, but none of them worked. Any idea? Best, Dani -- Daniel Valverde Saub? Grup de Biologia Molecular de Llevats Facultat de Veterin?ria de la Universitat Aut?noma de Barcelona Edifici V, Campus UAB 08193 Cerdanyola del Vall?s- SPAIN Centro de Investigaci?n Biom?dica en Red en Bioingenier?a, Biomateriales y Nanomedicina (CIBER-BBN) Grup d'Aplicacions Biom?diques de la RMN Facultat de Bioci?ncies Universitat Aut?...

...ay x <- 1:50 I would like it to be cut at certain points, being for example 1:5, 6:11, 12:17, ... How can I do it? I have tried the cut() function, but I don not know how to place the cutting points properly. Best regards, Dani -- Daniel Valverde Saub? Grup de Biologia Molecular de Llevats Facultat de Veterin?ria de la Universitat Aut?noma de Barcelona Edifici V, Campus UAB 08193 Cerdanyola del Vall?s- SPAIN Centro de Investigaci?n Biom?dica en Red en Bioingenier?a, Biomateriales y Nanomedicina (CIBER-BBN) Grup d'Aplicacions Biom?diques de la RMN Facultat de Bioci?ncies Universitat Aut?...

...g with '#' must be considered as comment lines. # 1628.40625 1628.40625 1964.40625 2242.0625 2533.5 2937.90625 3448.0 3923.96875 Is it possible to read it with R, something like scan() but keeping the structure? Best, Dani -- Daniel Valverde Saub? Grup de Biologia Molecular de Llevats Facultat de Veterin?ria de la Universitat Aut?noma de Barcelona Edifici V, Campus UAB 08193 Cerdanyola del Vall?s- SPAIN Centro de Investigaci?n Biom?dica en Red en Bioingenier?a, Biomateriales y Nanomedicina (CIBER-BBN) Grup d'Aplicacions Biom?diques de la RMN Facultat de Bioci?ncies Universitat Aut?...

...in code: lda.bootstrap As far as I undestand there is something present in lda.bootstrap.rd but not in lda.bootstrap.r. The problem is that everything appears in both files. Maybe I misundestand the error message. Any idea? Dani -- Daniel Valverde Saub? Grup de Biologia Molecular de Llevats Facultat de Veterin?ria de la Universitat Aut?noma de Barcelona Edifici V, Campus UAB 08193 Cerdanyola del Vall?s- SPAIN Centro de Investigaci?n Biom?dica en Red en Bioingenier?a, Biomateriales y Nanomedicina (CIBER-BBN) Grup d'Aplicacions Biom?diques de la RMN Facultat de Bioci?ncies Universitat Aut?...

Hello, I have two vectors, one with 13112 points and the other one with 10909. I wonder if there is a way to interpolate the data so the shorter vectors has the same number of points as the longer one. Best, Dani -- Daniel Valverde Saub? Grup de Biologia Molecular de Llevats Facultat de Veterin?ria de la Universitat Aut?noma de Barcelona Edifici V, Campus UAB 08193 Cerdanyola del Vall?s- SPAIN Centro de Investigaci?n Biom?dica en Red en Bioingenier?a, Biomateriales y Nanomedicina (CIBER-BBN) Grup d'Aplicacions Biom?diques de la RMN Facultat de Bioci?ncies Universitat Aut?...

...on of MASS package. I have plotted the LD1xLD2 to represent the data. Now I would like to get the centroids for each group of data and plot it on the LD1xLD2 graph. How can I get the centroid value from the lda object? Best, Dani -- Daniel Valverde Saub? Grup de Biologia Molecular de Llevats Facultat de Veterin?ria de la Universitat Aut?noma de Barcelona Edifici V, Campus UAB 08193 Cerdanyola del Vall?s- SPAIN Centro de Investigaci?n Biom?dica en Red en Bioingenier?a, Biomateriales y Nanomedicina (CIBER-BBN) Grup d'Aplicacions Biom?diques de la RMN Facultat de Bioci?ncies Universitat Aut?...

Hello, I would like to combine different label sizes in the same x-axis, for example 1 2 3 4 5 6 7 8 9 How can I do it? Best, Dani -- Daniel Valverde Saub? Grup de Biologia Molecular de Llevats Facultat de Veterin?ria de la Universitat Aut?noma de Barcelona Edifici V, Campus UAB 08193 Cerdanyola del Vall?s- SPAIN Centro de Investigaci?n Biom?dica en Red en Bioingenier?a, Biomateriales y Nanomedicina (CIBER-BBN) Grup d'Aplicacions Biom?diques de la RMN Facultat de Bioci?ncies Universitat Aut?...

...bject. I am interested on carrying out some kind of lsmeans on the data returned, but I cannot find any function to do this in R. I'have seen the effect() function, but it does not work with lme objects. Any idea? Best, Dani -- Daniel Valverde Saub? Grup de Biologia Molecular de Llevats Facultat de Veterin?ria de la Universitat Aut?noma de Barcelona Edifici V, Campus UAB 08193 Cerdanyola del Vall?s- SPAIN Centro de Investigaci?n Biom?dica en Red en Bioingenier?a, Biomateriales y Nanomedicina (CIBER-BBN) Grup d'Aplicacions Biom?diques de la RMN Facultat de Bioci?ncies Universitat Aut?...

Hello, I would like to convert an Rd object to a latex file, so that I can put it in my thesis. How can I do it? I tryed latex(), but it only works for code... Best, Dani -- Daniel Valverde Saub? Grup de Biologia Molecular de Llevats Facultat de Veterin?ria de la Universitat Aut?noma de Barcelona Edifici V, Campus UAB 08193 Cerdanyola del Vall?s- SPAIN Centro de Investigaci?n Biom?dica en Red en Bioingenier?a, Biomateriales y Nanomedicina (CIBER-BBN) Grup d'Aplicacions Biom?diques de la RMN Facultat de Bioci?ncies Universitat Aut?...

Hello, I would like to place some text that should appear in the same position of the graphic device, preferably outside the plotting area, regardless the x and y axes limits. How can I do this? Best, Dani -- Daniel Valverde Saub? Grup de Biologia Molecular de Llevats Facultat de Veterin?ria de la Universitat Aut?noma de Barcelona Edifici V, Campus UAB 08193 Cerdanyola del Vall?s- SPAIN Centro de Investigaci?n Biom?dica en Red en Bioingenier?a, Biomateriales y Nanomedicina (CIBER-BBN) Grup d'Aplicacions Biom?diques de la RMN Facultat de Bioci?ncies Universitat Aut?...

Hello, I have a sequence of numbers: seq(1:50) and I would like to have all the possible combinations with this numbers without repeating any combination: 11, 12, 13, ... ,22,23,24,... How can I do it? Best, Dani -- Daniel Valverde Saub? Grup de Biologia Molecular de Llevats Facultat de Veterin?ria de la Universitat Aut?noma de Barcelona Edifici V, Campus UAB 08193 Cerdanyola del Vall?s- SPAIN Centro de Investigaci?n Biom?dica en Red en Bioingenier?a, Biomateriales y Nanomedicina (CIBER-BBN) Grup d'Aplicacions Biom?diques de la RMN Facultat de Bioci?ncies Universitat Aut?...

...ta.spect[,2:13113]). When I try this code glmObject <- glm(data.spect[,2:13113]~data.spect[,1]) I get the following error: Error: (subscript) logical subscript too long Could anyone help me on solving this problem? Best, Dani -- Daniel Valverde Saub? Grup de Biologia Molecular de Llevats Facultat de Veterin?ria de la Universitat Aut?noma de Barcelona Edifici V, Campus UAB 08193 Cerdanyola del Vall?s- SPAIN Centro de Investigaci?n Biom?dica en Red en Bioingenier?a, Biomateriales y Nanomedicina (CIBER-BBN) Grup d'Aplicacions Biom?diques de la RMN Facultat de Bioci?ncies Universitat Aut?...

...ould like to perform an ANOVA on different variables. Is the call aov(Cr+mIb+...~Treatment, data=myMatrix) o correct way of doing it? What I would like to have is a p value for the variance for each response variable. Best, Dani -- Daniel Valverde Saub? Grup de Biologia Molecular de Llevats Facultat de Veterin?ria de la Universitat Aut?noma de Barcelona Edifici V, Campus UAB 08193 Cerdanyola del Vall?s- SPAIN Centro de Investigaci?n Biom?dica en Red en Bioingenier?a, Biomateriales y Nanomedicina (CIBER-BBN) Grup d'Aplicacions Biom?diques de la RMN Facultat de Bioci?ncies Universitat Aut?...

...)). This is the code: lme(Error ~ ID + Sequence + Temperature + Tumour) If I use this code, I get the following error: Error in getGroups.data.frame(dataMix, groups) : Invalid formula for groups Can anyone help me? Best, Dani -- Daniel Valverde Saub? Grup de Biologia Molecular de Llevats Facultat de Veterin?ria de la Universitat Aut?noma de Barcelona Edifici V, Campus UAB 08193 Cerdanyola del Vall?s- SPAIN Centro de Investigaci?n Biom?dica en Red en Bioingenier?a, Biomateriales y Nanomedicina (CIBER-BBN) Grup d'Aplicacions Biom?diques de la RMN Facultat de Bioci?ncies Universitat Aut?...

...lab=c(expression(Delta*delta)),xlab="pH") Which kind of model can I fit on these, so that can I predict for a given delta the pH of my sample? Once the model is fitted, how can I plot it on the graph? Best regards, Dani -- Daniel Valverde Saub? Grup de Biologia Molecular de Llevats Facultat de Veterin?ria de la Universitat Aut?noma de Barcelona Edifici V, Campus UAB 08193 Cerdanyola del Vall?s- SPAIN Centro de Investigaci?n Biom?dica en Red en Bioingenier?a, Biomateriales y Nanomedicina (CIBER-BBN) Grup d'Aplicacions Biom?diques de la RMN Facultat de Bioci?ncies Universitat Aut?...

...= pos, values = intensities) Can anyone help me on how can I solve it? I know that "pos" and "intensities" have the same length, so I don't know why I get this error. Any ideas will be welcome. Best, Dani -- Daniel Valverde Saub? Grup de Biologia Molecular de Llevats Facultat de Veterin?ria de la Universitat Aut?noma de Barcelona Edifici V, Campus UAB 08193 Cerdanyola del Vall?s- SPAIN Centro de Investigaci?n Biom?dica en Red en Bioingenier?a, Biomateriales y Nanomedicina (CIBER-BBN) Grup d'Aplicacions Biom?diques de la RMN Facultat de Bioci?ncies Universitat Aut?...

Hello, Is there any function like gsub(), that can match and replace patterns in a matrix or a data frame? Cheers! Dani -- Daniel Valverde Saub? Grup de Biologia Molecular de Llevats Facultat de Veterin?ria de la Universitat Aut?noma de Barcelona Edifici V, Campus UAB 08193 Cerdanyola del Vall?s- SPAIN Tlf. +34 93 581 1910 Fax: +34 93 581 1573

...oper way to analyze such a large data set? and 2) Is there an appropiate method for graphic plotting of my data, that takes into account the whole variability if my data, not just two principal components? Many thanks. Best, Dani -- Daniel Valverde Saub? Grup de Biologia Molecular de Llevats Facultat de Veterin?ria de la Universitat Aut?noma de Barcelona Edifici V, Campus UAB 08193 Cerdanyola del Vall?s- SPAIN Centro de Investigaci?n Biom?dica en Red en Bioingenier?a, Biomateriales y Nanomedicina (CIBER-BBN) Grup d'Aplicacions Biom?diques de la RMN Facultat de Bioci?ncies Universitat Aut?...

...able called R_PLATFORM. Now I need a full list of all the values this variable can have because I need to set an option depending on the endianness of the platform in which we are compiling the package. Anyone can help me? Thanks, Virgilio Gómez Rubio Dpto. Estadística e I. O. - Facultat de Matemàtiques Avda. Vicent A. Estellés, 1 - 46100 Burjassot Valencia - SPAIN TLF: 00 32 96 386 43 62 - FAX: 00 32 96 398 35 99 ---------- Forwarded message ---------- Date: Wed, 24 Jul 2002 10:24:14 +0200 (CEST) From: virgil@uv.es To: r-devel@lists.R-project.org Subject: Guessing o.s. during i...