gatk-3.8/perl/reports/1KG/pop_top_sheet_template.tex

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\documentclass[10pt]{article}
\usepackage[lmargin=0.3in, rmargin=0.3in, tmargin=0.9in, bmargin=0.9in, paperwidth=10.0in, paperheight=7.5in]{geometry}
\usepackage{multicol}
\usepackage{graphicx}
\usepackage{fancyhdr}
\pagestyle{fancy}
\begin{document}
\lhead{\bfseries{\Large{Sequencing and variant summary - $population$ samples}}}
\rhead{}
\chead{}
\begin{tabular}{|r|l|l|}
\multicolumn{3}{l}{\bfseries{Sequencing summary}} \\
\hline
& Lanes & Aligned Lanes \\
\hline
All & $allLanes$ & $allAlignedLanes$ \\
Passed QC & $passedQCLanes$ & $passedQCAlignedLanes$ \\
Failed Genotype QC & $failedGenotypeQCLanes$ & $failedGenotypeQCAlignedLanes$ \\
Failed one of the DCC processes & $failedDCCProcessLanes$ & $failedDCCProcessAlignedLanes$ \\
Not yet available from archive & $failedUnavailableLanes$ & $failedUnavailableAlignedLanes$ \\
Suppressed in archive & $failedSuppressedLanes$ & $failedSuppressedAlignedLanes$ \\
\hline
\end{tabular}
\begin{tabular}{|r|l|l|}
\multicolumn{3}{l}{\bfseries{Variant summary}} \\
\hline
& UnifiedGenotyper & QCALL \\
\hline
Called samples & $ugSamples$ & $qcallSamples$ \\
SNPs (all) & $ugAllSNPs$ & $qcallAllSNPs$ \\
Ti/Tv (all) & $ugAllTiTv$ & $qcallAllTiTv$ \\
SNPs (known) & $ugKnownSNPs$ & $qcallKnownSNPs$ \\
Ti/Tv (known) & $ugKnownTiTv$ & $qcallKnownTiTv$ \\
SNPs (novel) & $ugNovelSNPs$ & $qcallNovelSNPs$ \\
Ti/Tv (novel) & $ugNovelTiTv$ & $qcallNovelTiTv$ \\
\hline
\end{tabular}
\lfoot{}
\cfoot{}
\rfoot{\small{1,000 Genomes Automated Data Processing Report ($timestamp$)}}
\end{document}