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\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}
