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Commit 76683b1f authored by Olivier Langella's avatar Olivier Langella
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fiex little typo in doc (thanks to Céline Henry

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doc/images/tandem_filter.png

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doc/images/tandem_filter.png

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doc/images/tandem_filter.png
doc/images/tandem_filter.png
doc/images/tandem_filter.png
doc/images/tandem_filter.png
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......@@ -206,11 +206,11 @@ The filter window (Fig~\ref{filter}) defines the automated filtering process par
\item The protein E-value is the product of its valid unique peptide E-values and it is different from the protein E-values determined by X!Tandem.
\item The values are expressed in log(E-value).
\end{itemize}
\item[Sum to all] \hfill \\Defines how protein filter is performed when MS/MS results are combined :
\item[Apply protein filter to all samples together] \hfill \\Defines how protein filter is performed when MS/MS results are combined :
\begin{description}
\item[No] To validate a protein, the 2 parameters (peptide number and protein E-value) must be valid in at least one result.
\item[Disabled] To validate a protein, the 2 parameters (peptide number and protein E-value) must be valid in at least one result.
Interesting if one wants to compare SDS-PAGE-LC-MS/MS results, where peptides from a protein are in the same LC-MS/MS run.
\item[Yes] To validate a protein, the 2 parameters (peptide number and protein E-value) must be valid in the sum of all results.
\item[Enabled] To validate a protein, the 2 parameters (peptide number and protein E-value) must be valid in the sum of all results.
Interesting if one wants to compare 2DLC-MS/MS results, where peptides from a protein are split in different LC-MS/MS runs.
\end{description}
\item[Contaminants] \hfill \\When you perform an analysis using different fasta databases, you can remove the result from one database by selecting this database.
......@@ -236,8 +236,8 @@ After loading the results, you can select the result to view in the main window
\begin{itemize}
\item First frame "Identification Results" : choose the result to edit, displays the current number of samples and groups.
\item False Discovery Rate : estimates an FDR using a reverse/decoy database (see ~\ref{fdr})
\item Mass precision : computes the standard deviation between theoretical and observed mass of peptides (see ~\ref{standard_deviation})
\item False Discovery Rate : estimates an FDR using a reverse/decoy database %(see ~\ref{fdr})
\item Mass precision : computes the standard deviation between theoretical and observed mass of peptides %(see ~\ref{standard_deviation})
\item Filter identification results : choose criterium to validate identifications as described in ~\ref{filters}
\end{itemize}
......@@ -261,6 +261,7 @@ corresponding peptides;
\end{itemize}
\begin{figure}[!ht]
\label{prot}
\center \includegraphics[scale=0.5]{images/window_protein}
\caption{Proteins List}
\end{figure}
......
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