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\url{http://pappso.inra.fr/}\\ %\fancyhead{} \fancyfoot{} \rfoot{\thepage} -\lfoot{\includegraphics[width=1cm]{images/pappso.pdf}} +\lfoot{\includegraphics[width=1cm]{images/pappso}} \begin{document} @@ -106,7 +106,7 @@ At the firt start, the application open the configuration path window: \end{itemize} \begin{figure}[!ht] -\center \includegraphics[scale=0.5]{images/tandem_configuration.png} +\center \includegraphics[scale=0.5]{images/tandem_configuration} \caption{Configuration window} \label{configuration} \end{figure} @@ -124,7 +124,7 @@ Three successive graphical boxes help you select first the mzXML files or other To perform database searching, you must create or edit a model XML file (stored in the xtandem models folder). Open the menu \textit{Option $\rightarrow$ X!Tandem preset} (Fig~\ref{xtandem_parameter}). \begin{figure}[!ht] -\center \includegraphics[scale=0.4]{images/tandem_parameter.png} +\center \includegraphics[scale=0.4]{images/tandem_parameter} \caption{X!Tandem preset window} \label{xtandem_parameter} \end{figure} @@ -153,7 +153,7 @@ X!Tandem works with open peak-list files like mzXML, mgf, mzData, mzML or pkl fi X!Tandem software uses only protein databases in fasta format. It doesn't work with EST\footnote{Expressed Sequenced tag} sequences. You can transform your database using our application \textit{Protein database manager}, available \href{http://pappso.inra.fr/bioinformatique.html}{here}, or you can directly run it \href{http://pappso.inra.fr/documents/bioinformatique/database_manager.jnlp}{here}. \begin{figure}[!ht] -\center \includegraphics[scale=0.4]{images/tandem_analysis.png} +\center \includegraphics[scale=0.4]{images/tandem_analysis} \caption{X!Tandem parameter window} \label{xtandem_analysis} \end{figure} @@ -204,7 +204,7 @@ Interesting because it allows you to always include the same contaminant protein \end{description} \normalsize \begin{figure}[!ht] -\center \includegraphics[scale=0.5]{images/tandem_filter.png} +\center \includegraphics[scale=0.5]{images/tandem_filter} \caption{Filter window} \label{filter} \end{figure} @@ -229,7 +229,7 @@ After loading the results, you can select the result to view in the main window \begin{figure}[!ht] -\center \includegraphics[scale=0.5]{images/tandem_principal.png} +\center \includegraphics[scale=0.5]{images/tandem_principal} \caption{Main window} \label{principal} \end{figure} @@ -245,7 +245,7 @@ View the list of protein identified on the result. For more details on column se \end{itemize} \begin{figure}[!ht] -\center \includegraphics[scale=0.5]{images/window_protein.png} +\center \includegraphics[scale=0.5]{images/window_protein} \caption{Proteins List} \end{figure} @@ -254,7 +254,7 @@ View the list of protein identified on the result. For more details on column se View the protein sequence and coverage on a identified protein. To view this window, you must open it in the menu \textit{Windows $\rightarrow$ Protein details}. \begin{figure}[!ht] -\center \includegraphics[scale=0.7]{images/window_protein_detail.png} +\center \includegraphics[scale=0.7]{images/window_protein_detail} \caption{Protein details} \end{figure} @@ -269,7 +269,7 @@ View the peptides identified a protein. For more details on column see Fig~\ref{ \end{itemize} \begin{figure}[!ht] -\center \includegraphics[scale=0.5]{images/window_peptide.png} +\center \includegraphics[scale=0.5]{images/window_peptide} \caption{Peptides List} \end{figure} @@ -283,7 +283,7 @@ View the MS/MS spectra of an identified peptide. \end{itemize} \begin{figure}[!ht] -\center \includegraphics[scale=0.5]{images/window_peptide_detail.png} +\center \includegraphics[scale=0.5]{images/window_peptide_detail} \caption{Peptides Details} \end{figure} @@ -310,7 +310,7 @@ The export window (Fig~\ref{export}) shows the different types of available expo \end{description} \normalsize \begin{figure}[!ht] -\center \includegraphics[scale=0.5]{images/tandem_export.png} +\center \includegraphics[scale=0.5]{images/tandem_export} \caption{Export window} \label{export} \end{figure} @@ -344,7 +344,7 @@ The identified proteins are represented by sample (individual mode) or for all s \normalsize \begin{figure}[!ht] -\center \includegraphics[width=1.0\textwidth]{images/tandem_prot.pdf} +\center \includegraphics[width=1.0\textwidth]{images/tandem_prot} \caption{Protein results} \label{prot} \end{figure} @@ -381,7 +381,7 @@ Identified peptides are grouped by group (Fig~\ref{pep}). One line corresponds t \normalsize \begin{figure}[!ht] -\center \includegraphics[width=1.0\textwidth]{images/tandem_peptide.pdf} +\center \includegraphics[width=1.0\textwidth]{images/tandem_peptide} \caption{Peptide results} \label{pep} \end{figure} @@ -412,7 +412,7 @@ The list of proteins is repeated 4 times, corresponding to the 4 parameters that \normalsize \begin{figure}[!ht] -\center \includegraphics[width=1.0\textwidth]{images/tandem_comparaison.pdf} +\center \includegraphics[width=1.0\textwidth]{images/tandem_comparaison} \caption{Comparison results} \label{compar} \end{figure} @@ -427,7 +427,7 @@ In this case, the column corresponding to the normal and reverse search are indi \end{itemize} \begin{figure}[!ht] -\center \includegraphics[scale=0.5]{images/tandem_fdr.png} +\center \includegraphics[scale=0.5]{images/tandem_fdr} \caption{FDR results} \label{fdr2} \end{figure}