<tool id="recetox_aplcms_hybrid" name="apLCMS - Hybrid" version="@TOOL_VERSION@+galaxy1">
    <macros>
        <import>aplcms_macros.xml</import>
    </macros>

    <expand macro="requirements" />

    <command detect_errors="aggressive"><![CDATA[
        #set file_str = str('", "').join([str($f) for $f in $files])

        Rscript
            -e 'x <- apLCMS::hybrid(
                    files = c("$file_str"),
                    known_table = apLCMS::load_known_table_from_hdf("$known_table"),
                    min_exp = $noise_filtering.min_exp,
                    min_pres = $noise_filtering.min_pres,
                    min_run = $noise_filtering.min_run,
                    mz_tol = $noise_filtering.mz_tol,
                    baseline_correct = $noise_filtering.baseline_correct,
                    baseline_correct_noise_percentile = $noise_filtering.baseline_correct_noise_percentile,
                    intensity_weighted = $noise_filtering.intensity_weighted,
                    shape_model = "$feature_detection.shape_model",
                    BIC_factor = $feature_detection.BIC_factor,
                    peak_estim_method = "$feature_detection.peak_estim_method",
                    min_bandwidth = $feature_detection.min_bandwidth,
                    max_bandwidth = $feature_detection.max_bandwidth,
                    sd_cut = c($feature_detection.sd_cut_min, $feature_detection.sd_cut_max),
                    sigma_ratio_lim = c($feature_detection.sigma_ratio_lim_min, $feature_detection.sigma_ratio_lim_max),
                    component_eliminate = $feature_detection.component_eliminate,
                    moment_power = $feature_detection.moment_power,
                    align_chr_tol = $peak_alignment.align_chr_tol,
                    align_mz_tol = $peak_alignment.align_mz_tol,
                    max_align_mz_diff = $peak_alignment.max_align_mz_diff,
                    match_tol_ppm = $history_db.match_tol_ppm,
                    new_feature_min_count = $history_db.new_feature_min_count,
                    recover_mz_range = $weak_signal_recovery.recover_mz_range,
                    recover_chr_range = $weak_signal_recovery.recover_chr_range,
                    use_observed_range = $weak_signal_recovery.use_observed_range,
                    recover_min_count = $weak_signal_recovery.recover_min_count
                )'
            -e 'apLCMS::save_peaks_to_hdf("$peaks", x)'
            -e 'apLCMS::save_known_table_to_hdf("$updated_known_table", x\$updated_known_table)'
    ]]></command>

    <expand macro="inputs">
        <expand macro="history_db" />
        <expand macro="noise_filtering" />
        <expand macro="feature_detection" />
        <expand macro="peak_alignment" />
        <expand macro="weak_signal_recovery" />
    </expand>

    <outputs>
        <data name="peaks" format="h5" />
        <data name="updated_known_table" format="h5" />
    </outputs>

    <tests>
        <test>
            <param name="files" value="mbr_test0.mzml,mbr_test1.mzml,mbr_test2.mzml" ftype="mzml"/>
            <param name="known_table" value="known_table.h5" ftype="h5"/>
            <output name="peaks" file="peaks_hybrid.h5" ftype="h5" compare="sim_size" delta="1000"/>
        </test>
    </tests>

    <help>
        This is the Hybrid version of apLCMS which is incorporating the knowledge of known metabolites and historically
        detected features on the same machinery to help detect and quantify lower-intensity peaks.

        CAUTION: To use such knowledge, especially historical data, you must keep using (1) the same chromatography
        system (otherwise the retention time will not match), and (2) the same type of samples with similar extraction
        technique, such as human serum.

        @GENERAL_HELP@
    </help>

    <expand macro="citations" />
</tool>