From: <cri...@de...> - 2002-12-31 09:33:03
|
Hello, I have a problem with a table I have to do for a report. The first line only has three columns, the second line 5 columns, the third line 7 columns. I have been not capable of doing this table because: 1) The first line appears with 4 columns and the last column does not close with a || as I wanted to. 2) The table gets out of the page when a dvi or a ps file is created. I can only see until the the middle of the 6th column. 3) The second line is not correctly positioned. The second and third column should be below the second column of first line and are not. Further, I wanted the third column to close with || and it does not. Below I send the code I use to generate this table. Can anyone help me and explain me how to fix these problems? Once I understand how to fix these problems I guess I understand how multicolumn works. Do you know if there is any type of .sty to work with more sophisticated columns? Thanks in advance Cristina \begin{table}[hbt] \begin{center} \begin{tabular}{||c||c|c|c||c|c|c||} \hline \hline F points & \multicolumn{2}{c||}{$\Delta \omega > 0$} & \multicolumn{2}{c||}{$\Delta \omega < 0$} \\ \hline \hline & $c > 0$ & \multicolumn{2}{c|}{$c <0$} & $c < 0$ & \multicolumn{2}{c|}{$c > 0 $} \\ \hline & & $\Delta \omega < 2 c \sin (-\theta) $ & $\Delta \omega > 2 c \sin (-\theta) $ & & $\Delta \omega < 2 c \sin (-\theta) $ $\Delta \omega > 2 c \sin (-\theta) $\\ \hline $\phi_1$ & Stable & Unstable & Stable & Unstable & Stable & Unstable \\ \hline $\phi_2$ & Unstable & Stable & Stable & Stable & Unstable & Stable \\ \hline \hline \end{tabular} \end{center} \caption{Fixed points and stability conditions of Eq.~(\ref{eq:relativephase}).} \label{tab:stabrelativephase} \end{table} |
From: Armin R. <xa...@bi...> - 2002-12-31 10:51:08
|
I put some auxillary text into a table environment in order to have it as a floating box inserted in the main text. The problem is that it always floats to the very end of the text rather than to the top of the next page. This is not the case when the table is less than half a page short. 1. Is there another floating environment besides FIGURE and TABLE, maybe something like "textbox" that may be more suitable to my purpose? 2. (Even if the answer to 1. is positive,) How do I direct tables that fill like 80% of a page to be placed inside the text rather than in the end? 3. A different table problem: I have a number of empty fiels in my table and do NOT want right and left border lines to appear next to the empty fields. Inside the table, I can do that with \multicolumn. However, I can't manage to remove the borderline if it is on the extreme right or left, i.e. at the edge rather than between two cells. Below I am pasting the long table text box mentioned above. I'd appreciate any hints. Thanks a lot! Armin ---------------- \begin{table}[htb] \fbox{\parbox{15cm}{\sloppy \bfseries SAGE: Basic principle \mdseries A very brief description of SAGE library construction should aid the understanding of our analysis: RNA is isolated and magnetic bead-linked poly-T primers are used to generate cDNA transcripts. Once double-stranded cDNA is obtained, it is cut with the "anchoring enzyme" NlaIII, a restriction enzyme specific for CATC. The library of NlaIII-restricted 3'-tail sequences is isolated by magnetic separation. Next, adapters are ligated to the cDNA ends. The adapters contain PCR primer binding sites and a "tagging enzyme" binding site directly adjacent to a CATC overhang to bind to the NlaIII-restricted ends. As a tagging enzyme, BsmFI is used, a restriction enzyme with the recognition sequence GGACN$_{10}$/N$_{14}$. The point is that BsmF1 binds on the primer but cuts inside the unknown sequence. Once the adapters are ligated, the product is digested with BsmFI and the overhang is filled in to yield blunt ends. Magnetic beads coupled tails are discarded and the reaction products are blunt-end ligated to each-other and amplified by PCR from the primer binding sequences on the adapters. Only tag-to-tag ligated dimers (ditags) are amplified. Ditags cut out with the anchoring enzyme NlaIII and isolated by agarose gel electrophoresis, then ligated to each-other to form ditag-NlaIII site oligomers. Oligomers of suitable length for sequencing are isolated by agarose gel electrophoresis and ligated into a proper vector which has sequencing primer binding sites. BsmFI cuts with an overhand of 14bp. Due to adapter design, the first four bases are the NlaIII cutting site, the following 10 are specific to the mRNA. Therefore, the method has a base pair specificity of $4^{14}=2.5*10^8$ and there are $4^10=10^6$ possible tags, approximately 40x the number of human genes. (To be precise, the specificity is even greater because not any NlaIII sites are determined, but only the most 3' one of each mRNA, assuming complete digestion. On the other hand, our estimate does not consider splice variants even though differential splicing on the 3' side of mRNAs is likely to yield distinct SAGE tags.) Although a few tags are known to represent multiple genes, most tags represent only a single gene which can be determined by searching sequence databases. The method is not limited or biased to mRNA tags already in a database, tags to novel genes can be identified in preexisting SAGE data sets. A problem is posed by the redundancy of information in sequence databases: A single gene often has several entries in the form of mRNA variants and ESTs. The UniGene catalogue of human genes \citep{schu97a} clusters redundant sequences in data bases which identify the same gene and gives them a common identification number, the UniGene cluster ID. SAGE tags have been linked to UniGene clusters. }} \caption[SAGE: principle]{\label{tab:res:aboutsage}SAGE: A brief explanation} \end{table} |
From: Roberto B. <rba...@uo...> - 2002-12-31 14:05:49
|
Dear Armin, the behaviour described is controlled by the float placement parametres (topnumber, bottomnumber, totalnumber, textfraction, topfraction, bottomfraction and floatpagefraction). Change them and you may achieve what you want. You may also want to read chapters 16 and 17 of "Using Imported Graphics with LaTeX2e" by Keith Reckdahl (texmf\doc\latex\graphic\epslatex.ps in my old MiKTeX 1.20 or search CTAN for epslatex). An example showing how to change the parametres follows (you will have to play with the parametres to find the solution to your case.) %%%%%%%%%%%%Float Placement Parametres%%%%%%%%%% %\setcounter{topnumber}{} %default=2 \setcounter{bottomnumber}{2} %default=1 \setcounter{totalnumber}{4} %default=3 %\renewcommand{\textfraction}{} %default=0.2 \renewcommand{\topfraction}{0.8} %default=0.7 %\renewcommand{\bottomfraction}{} %default=0.3 %\renewcommand{\floatpagefraction}{} %default=0.5 %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% Regards, Roberto Armin Rump wrote: > I put some auxillary text into a table environment in order to > have it as a floating box inserted in the main text. > > The problem is that it always floats to the very end of the text > rather than to the top of the next page. This is not the case > when the table is less than half a page short. > > 1. Is there another floating environment besides FIGURE and > TABLE, maybe something like "textbox" that may be more suitable > to my purpose? > > 2. (Even if the answer to 1. is positive,) How do I direct > tables that fill like 80% of a page to be placed inside the text > rather than in the end? > > 3. A different table problem: > I have a number of empty fiels in my table and do NOT want right > and left border lines to appear next to the empty fields. > Inside the table, I can do that with \multicolumn. However, I > can't manage to remove the borderline if it is on the extreme > right or left, i.e. at the edge rather than between two cells. > > > Below I am pasting the long table text box mentioned above. I'd > appreciate any hints. > Thanks a lot! > > Armin > > ---------------- > > \begin{table}[htb] > \fbox{\parbox{15cm}{\sloppy > > \bfseries SAGE: Basic principle \mdseries > > A very brief description of SAGE library construction should aid > the understanding of our analysis: > > RNA is isolated and magnetic bead-linked poly-T primers are used > to generate cDNA transcripts. Once double-stranded cDNA is > obtained, it is cut with the "anchoring enzyme" NlaIII, a > restriction enzyme specific for CATC. The library of > NlaIII-restricted 3'-tail sequences is isolated by magnetic > separation. > > Next, adapters are ligated to the cDNA ends. The adapters contain > PCR primer binding sites and a "tagging enzyme" binding site > directly adjacent to a CATC overhang to bind to the > NlaIII-restricted ends. As a tagging enzyme, BsmFI is used, a > restriction enzyme with the recognition sequence > GGACN$_{10}$/N$_{14}$. The point is that BsmF1 binds on the > primer but cuts inside the unknown sequence. > > Once the adapters are ligated, the product is digested with BsmFI > and the overhang is filled in to yield blunt ends. Magnetic beads > coupled tails are discarded and the reaction products are > blunt-end ligated to each-other and amplified by PCR from the > primer binding sequences on the adapters. Only tag-to-tag ligated > dimers (ditags) are amplified. > > Ditags cut out with the anchoring enzyme NlaIII and isolated by > agarose gel electrophoresis, then ligated to each-other to form > ditag-NlaIII site oligomers. Oligomers of suitable length for > sequencing are isolated by agarose gel electrophoresis and ligated > into a proper vector which has sequencing primer binding sites. > > BsmFI cuts with an overhand of 14bp. Due to adapter design, the > first four bases are the NlaIII cutting site, the following 10 are > specific to the mRNA. Therefore, the method has a base pair > specificity of $4^{14}=2.5*10^8$ and there are $4^10=10^6$ > possible tags, approximately 40x the number of human genes. (To > be precise, the specificity is even greater because not any NlaIII > sites are determined, but only the most 3' one of each mRNA, > assuming complete digestion. On the other hand, our estimate does > not consider splice variants even though differential splicing on > the 3' side of mRNAs is likely to yield distinct SAGE tags.) > Although a few tags are known to represent multiple genes, most > tags represent only a single gene which can be determined by > searching sequence databases. The method is not limited or biased > to mRNA tags already in a database, tags to novel genes can be > identified in preexisting SAGE data sets. > > A problem is posed by the redundancy of information in sequence > databases: A single gene often has several entries in the form of > mRNA variants and ESTs. The UniGene catalogue of human genes > \citep{schu97a} clusters redundant sequences in data bases which > identify the same gene and gives them a common identification > number, the UniGene cluster ID. SAGE tags have been linked to > UniGene clusters. > > }} \caption[SAGE: principle]{\label{tab:res:aboutsage}SAGE: A > brief explanation} > \end{table} > > > > ------------------------------------------------------- > This sf.net email is sponsored by:ThinkGeek > Welcome to geek heaven. > http://thinkgeek.com/sf > _______________________________________________ > MiKTeX-Users mailing list > MiK...@li... > https://lists.sourceforge.net/lists/listinfo/miktex-users |
From: Andre V. R. <av...@pa...> - 2002-12-31 11:19:56
|
Is this what you want? Andre \documentclass[dutch,a4paper,twoside,10pt]{article} \special{papersize=297mm,210mm} \begin{document} \begin{table}[hbt] \begin{center}\tiny%\footnotesize \begin{tabular}{||c||c|c||c|c|c|c||} \hline \hline F points & \multicolumn{2}{c||}{$\Delta \omega > 0$} & \multicolumn{4}{c||}{$\Delta \omega < 0$} \\ \hline \hline & $c > 0$ & \multicolumn{1}{c||}{$c <0$} & $c < 0$ & \multicolumn{3}{c||}{$c > 0 $} \\ \hline & & $\Delta \omega < 2 c \sin (-\theta) $ & $\Delta \omega > 2 c \sin (-\theta) $ & & $\Delta \omega < 2 c \sin (-\theta) $ & $\Delta \omega > 2 c \sin (-\theta) $\\ \hline $\phi_1$ & Stable & Unstable & Stable & Unstable & Stable & Unstable \\ \hline $\phi_2$ & Unstable & Stable & Stable & Stable & Unstable & Stable \\ \hline \hline \end{tabular} \end{center} \caption{Fixed points and stability conditions of Eq.~(\ref{eq:relativephase}).} \label{tab:stabrelativephase} \end{table} \end{document} > |
From: <zar...@un...> - 2002-12-31 11:49:23
|
cri...@de... wrote: > > Hello, > > I have a problem with a table I have to do for a report. The first line only [snip] > Hi, your table is to long to be fitted in width of text. I see, that 6th column is very broad, actualy I dont understand the mining of expresin $\Delta \omega < 2 c \sin (-\theta) $ $\Delta \omega > 2 c \sin (-\theta) $ in it. if you omit second math expresion, table can be fit in textwidth. Regarding to latex you have more possibilities to fit you table in desired width. One is use package tabularx and define appropriate column type, like \newcolumntype{C}{>{\centering\arraybackslash}X} \newcolumntype{L}{>{\raggedright\arraybackslash}X} \newcolumntype{R}{>{\raggedleft\arraybackslash}X} (for detail see The LaTeX companion /Goossens, Mittelbach, Samarin/) if you need more than centering position in column. For your table it is enought to replace \begin{tabular}... \end{tabular} with \documentclass{article}%report, book, etc \usepackage{tabularx} \begin{document} \begin{table} \begin{tabularx}{\textwidth}{||X||X|X|X||X|X|X||} ... \end{tabularx} \end{table} \end{documetn} Second posibilities is to handy calculate desired width of column and use "p{width}" instead of "c", for example \begin{tabular}{||p{2cm}||p{2cm}|p{2cm}|p{2cm}||p{2cm}|p{2cm}|p{2cm}||} ... \end{tabular} If you liked to have centered content in column, you can define new column type similar as above, for example \newcolumntype{C}{>{\centering\arraybackslash}p} Another posibilities is to put the table in "landscape" position. For this you probably need package rotating: \documentclass{article}%report, book, etc \usepackage{rotating \begin{sidewaystable} \begin{tabular}{\textwidth}{||c||c|c|c||c|c|c||} ... \end{tabular} \end{sidewaystable} \end{documetn} (for details please read documentacion with rotating package). Maybe will be helpfull also to look in http://www.tex.ac.uk/cgi-bin/texfaq2html?label=fixwidtab For omiting of vertical lines in last columns is probably "guilty" bug, since Latex should reported that number of columns in your first and third row is not in accordance width your declaration (you have only 5 columns in first row and 6 columns in third row instead of declared 7). If you will put approptiate number of signs & or number of merged column in multicolumn, this problem will disipear. You can also use smaller characters as you can already read in another unswer I hope that his will help you a litle bit regards and Happy New Year Zarko |