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Understanding the BaseSpace HTML reports

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Summary results

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Sample Composition

The Sample Composition bargraphs show the proportion of reads classified to six broad categories for of all samples in the analysis run: Targeted Microbial, Untargeted, Ambiguous, Unclassified, Low Complexity, and Targeted Internal Control (RPIP, UPIP, VSP V2 only).

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Summary Statistics

The Summary Statistics table summarizes sample QC metrics for all samples in the analysis run. Further details on each metric can be found by hovering over each column header.

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Per sample results

Individual sample results can be further explored by clicking on "Report" under each sample name in the panel on the left. There are four tabs in the Sample Report: Sample Quality Control, Microorganisms, Antimicrobial Resistance Markers, and User Options.

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1. Sample Quality Control

  • Version Information is a table with the application version, test type, and test version that were run. Running the latest version of the application is recommended.

  • Sample Composition is a bargraph showing the proportion of post-quality reads classified to six broad categories for the sample (RPIP, UPIP, VSP V2 only).

  • Read Classification is a dynamic plot that can be configured to show the following (RPIP, UPIP, VSP V2 only):

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2. Microorganisms

  • Microorganism results are summarized in tables, separated by type (Viruses, Bacteria, Fungi, Parasites). Each table includes whether the microorganism is predicted present in the sample, as well as various alignment metrics. Further details on each metric can be found by hovering over each column header. The best-match Reference Accession(s) are provided for all RPIP, RVOP/RVEK, VSP, and VSP V2 viruses in the Viruses table. To see all best-match Reference Accession(s), click on the three dots (...) in the table and scroll down the page.

  • Reference Coverage is a dynamic plot showing the coverage depth across the viral genome for detected RPIP, RVOP/RVEK, VSP, and VSP V2 viruses. Select a virus from the dropdown list to view the coverage plot. Segments are concatenated for segmented viruses, and the targeted regions of the viral genome are indicated for RPIP viruses.

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3. Antimicrobial Resistance Markers

  • Viral AMR (Variants) is a table with viral AMR variant results for Influenza A/B viruses (RPIP, RVOP/RVEK, VSP, and VSP V2 only)

  • Bacterial AMR (Genes) is a table witb bacterial AMR gene results (RPIP, UPIP only)

  • Bacterial AMR (Variants) is a table with bacterial AMR variant results (RPIP, UPIP only)

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4. User Options

The User Options table summarizes user options selected during launch of the analysis.

Output files

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Note: Some files may not be generated depending on the selected analysis options and analysis results

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Sample-level output files

Filename

Targeted Microbial Reads - Relative (default): Bargraph of post-quality targeted microbial reads belonging to Viral, Bacterial, Fungal, Parasite and AMR categories, relative to post-quality targeted microbial reads only. Percentages are expected to sum to 100%. Hover over an individual bar to display the values.

  • Targeted Microbial Reads - Absolute: Bargraph of post-quality targeted microbial reads belonging to Viral, Bacterial, Fungal, Parasite and AMR categories for all post-quality reads in the sample overall. Hover over an individual bar to display the values.

  • Untargeted Reads - Relative: Bargraph of post-quality untargeted reads belonging to untargeted categories, relative to post-quality untargeted reads only. Percentages are expected to sum to 100%. Hover over an individual bar to display the values.

  • Untargeted Reads - Absolute: Bargraph of post-quality untargeted reads belonging to untargeted categories for all post-quality reads in the sample overall. Hover over an individual bar to display the values.

    **Note that accurate sample composition and read classification results rely on selecting the correct enrichment panel. If you run an analysis that is not specific to the enrichment panel (e.g., VSP V2 analysis with VSP-enriched samples), reads from high background viruses that are not targeted by VSP probes (e.g., Measles virus) but that are targeted by VSP V2 probes will be reported as targeted viral reads.

  • Internal Controls is a table containing supported Internal Control options along with observed RPKM values (RPIP, UPIP, VSP V2 only).

  • QC Metrics is a table containing sample QC metrics. Dehosting refers to human reads only.

  • Type
    Description

    Samplename.Panelname.report.json

    json

    Comprehensive report file. See for further details

    Samplename.Panelname.report.html

    html

    Visual report file. See for further details

    Samplename.Panelname.viral_variants.vcf

    vcf

    Viral variant call file describing variant calls between viral consensus genome (or segment) sequences and best-match reference sequences (all RVOP/RVEK, VSP, and VSP V2 viruses, RPIP: SARS-CoV-2 & FluA/B/C only)

    Samplename.Panelname.viral_genomes_consensus.fa

    fasta

    Viral genome (or segment) nucleotide consensus sequence(s) for all viruses reported in the sample (RPIP, RVOP/RVEK, VSP, VSP V2 only)

    Samplename.Panelname.viral_targets_consensus.fa

    fasta

    Viral targeted region nucleotide consensus sequence(s) for all viruses reported in the sample (RPIP only)

    Samplename.Panelname.bacterial_amr_nucleotide_consensus.fa

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    Analysis-level output files

    Filename
    Type
    Description

    AnalysisIDnumber.Panelname.results.zip

    zip

    Compressed file containing all output files for single-click download

    AnalysisIDnumber.Panelname.report.xlsx

    xlsx

    Aggregate Excel report file that summarizes results for all samples across 4 tabs: Samples, Microorganisms, AMR, and Variants. See below for further details

    report.html

    html

    Visual report file. See for further details

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    DMEplus_aggregate_report_descriptions.xlsx
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    RPIP, UPIP, RVOP/RVEK, VSP, VSP V2: Description of aggregate Excel report file fields
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    DMEplus_custom_aggregate_report_descriptions.xlsx
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    Custom Panel: Description of aggregate Excel report file fields

    fasta

    Bacterial AMR gene nucleotide consensus sequence(s) for all bacterial AMR markers reported in the sample (RPIP, UPIP only)

    Samplename.Panelname.bacterial_amr_protein_consensus.fa

    fasta

    Bacterial AMR gene protein consensus sequence(s) for all bacterial AMR markers reported in the sample (RPIP, UPIP only)

    viral_consensus_genomes

    Dataset

    Directory containing viral genome (or segment) nucleotide consensus sequence(s) per virus reported in the sample (RPIP, RVOP/RVEK, VSP, VSP V2 only)

    Report JSON format
    Understanding the BaseSpace HTML reports
    Understanding the BaseSpace HTML reports

    Report JSON format

    The DRAGEN Microbial Enrichment Plus app outputs a comprehensive sample-level report.json file containing general metadata, version information, sample QC, microorganism, and AMR marker results, as well as detailed test information. The additional convenience file formats generated by the DRAGEN Microbial Enrichment Plus app do not contain novel content.

    (*) indicates results generated by the application layer as opposed to the DRAGEN secondary analysis pipeline

    Top-Level Node

    The top-level section of the report JSON contains general metadata and version information.

    Field
    Description

    .qcReport.sampleQc Node

    This section contains information about sample quality control (QC). The fields are relative to .qcReport.sampleQc

    Field
    Description

    .qcReport.enrichmentFactor Node

    This section contains information about the enrichment factor calculation and is relevant to RPIP, UPIP, and VSP V2 only. Detection of an appropriate Internal Control is required. The fields are relative to .qcReport.enrichmentFactor

    Field
    Description

    .qcReport.sampleComposition Node

    This section contains information about the composition of the sample and is provided for RPIP, UPIP, and VSP V2 only. The fields are relative to .qcReport.sampleComposition

    Field
    Description

    .qcReport.internalControls Node

    This section contains information about internal control detection and is relevant to RPIP, UPIP, and VSP V2 only. The value of the .qcReport.internalControls field is an array of objects containing name and RPKM information for each Internal Control. See the code block below for an example:

    .userOptions Node

    This section gives information about analysis options specified by the user. The fields are relative to .userOptions

    Field
    Description

    .targetReport.microorganisms[] Node

    The value of the .targetReport.microorganisms[] field is an array of objects containing information about detected microorganisms. The following table describes one .targetReport.microorganisms[] object. The fields are relative to .targetReport.microorganisms[]

    Field
    Description

    .targetReport.microorganisms[].predictionInformation[].relatedMicroorganisms[] Node

    The value of the .targetReport.microorganisms[].predictionInformation[].relatedMicroorganisms[] field is an array of objects containing information about genetically related microorganisms. The following table describes one .targetReport.microorganisms[].predictionInformation[].relatedMicroorganisms[] object. The fields are relative to .targetReport.microorganisms[].predictionInformation[].relatedMicroorganisms[]

    Field
    Description

    .targetReport.microorganisms[].variants[] Node

    The value of the .targetReport.microorganisms[].variants[] field is an array of objects containing information about viral variants for all RVOP/RVEK, VSP, and VSP V2 viruses, RPIP: SARS-CoV-2 & FluA/B/C only. The following table describes one .targetReport.microorganisms[].variants[] object. The fields are relative to .targetReport.microorganisms[].variants[]

    Field
    Description

    .targetReport.microorganisms[].pangoLineage[] Node

    The value of the .targetReport.microorganisms[].pangoLineage[] field is an array of objects containing information about SARS-CoV-2 Pango lineage prediction results. The following table describes one .targetReport.microorganisms[].pangoLineage[] object. The fields are relative to .targetReport.microorganisms[].pangoLineage[].

    .targetReport.microorganisms[].nextclade[] Node

    The value of the .targetReport.microorganisms[].nextclade[] field is an array of objects containing information about viral clade assignment results for applicable viruses. The following table describes one .targetReport.microorganisms[].nextclade[] object. The fields are relative to .targetReport.microorganisms[].nextclade[].

    .targetReport.amrMarkers[] Node

    The value of the .targetReport.amrMarkers[] field is an array of objects containing information about detected bacterial AMR markers. The following table describes one .targetReport.amrMarkers[] object. The fields are relative to .targetReport.amrMarkers[]

    Field
    Description

    .targetReport.amrMarkers[].variants[] Node

    The value of the .targetReport.amrMarkers[].variants[] field is an array of objects containing information about variants for bacterial AMR markers with "protein variant" or "rRNA variant" model types. The following table describes one .targetReport.amrMarkers[].variants[] object. The fields are relative to .targetReport.amrMarkers[].variants[]

    Field
    Description

    .targetReport.customReferences[] Node

    This section contains information about custom reference detection results and is only present for custom database analyses. When only a custom reference FASTA file is provided (no BED file), each .targetReport.customReferences[] object contains information for a single reference sequence. When both a FASTA and BED file are provided, each .targetReport.customReferences[] object contains information for a single genome/microorganism, which can be a collection of one or more reference sequences. The fields are relative to .targetReport.customReferences[]

    Field
    Description

    .targetReport.customReferences[].consensusSequences[] Node

    The value of the .targetReport.customReferences[].consensusSequences[] field is an array of objects containing majority consensus sequence information for a single custom reference sequence. When only a FASTA file is provided (no BED file), there will be only one object in the array. When both a FASTA and BED file are provided, there may be more than one object in the array. The fields are relative to .targetReport.customReferences[].consensusSequences[]

    Field
    Description

    .targetReport.customReferences[].variants[] Node

    The value of the .targetReport.customReferences[].variants[] field is an array of objects containing information about a single detected variant. The fields are relative to .targetReport.customReferences[].variants[]

    Field
    Description

    .targetReport.customReferences[].pangoLineage[] Node

    The value of the .targetReport.customReferences[].pangoLineage[] field is an array of objects containing information about SARS-CoV-2 Pango lineage prediction results. The following table describes one .targetReport.customReferences[].pangoLineage[] object. The fields are relative to .targetReport.customReferences[].pangoLineage[]

    .additionalInformation[] Node

    The value of the .additionalInformation[] field is an array of objects containing additional information about the test and data analysis solution. The fields are relative to .additionalInformation[]

    Field
    Description

    .postQualityReads

    Number of reads in sample after read QC processing, inclusive of any duplicate reads

    .postQualityReadsProportion

    Proportion of post-quality reads in sample relative to total raw reads

    .removedInDehostingReads

    Number of host reads in sample removed during dehosting (host = human)

    .removedInDehostingReadsProportion

    Proportion of host reads in sample removed relative to total raw reads (host = human)

    .entropy

    Shannon entropy of the counts of 5-mers in the reads after read QC processing, which is a measure of randomness

    .gContent

    Proportion of guanine (G) base calls in reads after read QC processing

    .libraryQScore

    Quality score of the library after read QC processing

    .readClassification.lowComplexity

    Low complexity

    .targetedMicrobial

    Proportion of post-quality targeted microbial reads classified to the following sub-categories:

    .targetedMicrobial.viral

    Viral targeted

    .targetedMicrobial.bacterial

    Bacterial targeted

    .targetedMicrobial.fungal

    Fungal targeted

    .targetedMicrobial.parasitic

    Parasitic targeted

    .targetedMicrobial.bacterialAmr

    Bacterial AMR targeted

    .untargeted

    Proportion of post-quality untargeted reads classified to the following sub-categories:

    .untargeted.viral

    Viral untargeted

    .untargeted.bacterial

    Bacterial untargeted

    .untargeted.fungal

    Fungal untargeted

    .untargeted.parasitic

    Parasitic untargeted

    .untargeted.bacterialAmr

    Bacterial AMR untargeted

    .untargeted.internalControl

    Internal Control untargeted

    .untargeted.human

    Human untargeted

    .viral

    Proportion of post-quality viral reads classified to the following categories:

    .viral.targeted

    Viral targeted

    .viral.untargeted

    Viral untargeted

    .viral.untargetedSubcategories

    Proportion of post-quality viral untargeted reads classified to the following sub-categories:

    .viral.untargetedSubcategories.panel

    Viral panel members

    .viral.untargetedSubcategories.phage

    Viral phage

    .viral.untargetedSubcategories.other

    Viral other (not a panel member or phage)

    .bacterial

    Proportion of post-quality bacterial reads classified to the following categories:

    .bacterial.targeted

    Bacterial targeted

    .bacterial.untargeted

    Bacterial untargeted

    .bacterial.untargetedSubcategories

    Proportion of post-quality bacterial untargeted reads classified to the following sub-categories:

    .bacterial.untargetedSubcategories.panel

    Bacterial panel members

    .bacterial.untargetedSubcategories.ribosomalDna

    Bacterial ribosomal DNA (16S)

    .bacterial.untargetedSubcategories.plasmid

    Bacterial plasmids

    .bacterial.untargetedSubcategories.other

    Bacterial other (not a panel member, ribosomal DNA, or plasmid)

    .fungal

    Proportion of post-quality fungal reads classified to the following categories:

    .fungal.targeted

    Fungal targeted

    .fungal.untargeted

    Fungal untargeted

    .fungal.untargetedSubcategories

    Proportion of post-quality fungal untargeted reads classified to the following sub-categories:

    .fungal.untargetedSubcategories.panel

    Fungal panel members

    .fungal.untargetedSubcategories.ribosomalDna

    Fungal ribosomal DNA (18S)

    .fungal.untargetedSubcategories.other

    Fungal other (not a panel member or ribosomal DNA)

    .parasitic

    Proportion of post-quality parasitic reads classified to the following categories:

    .parasitic.targeted

    Parasitic targeted

    .parasitic.untargeted

    Parasitic untargeted

    .parasitic.untargetedSubcategories

    Proportion of post-quality parasitic untargeted reads classified to the following sub-categories:

    .parasitic.untargetedSubcategories.panel

    Parasitic panel members

    .parasitic.untargetedSubcategories.ribosomalDna

    Parasitic ribosomal DNA (18S)

    .parasitic.untargetedSubcategories.other

    Parasitic other (not a panel member or ribosomal DNA)

    .human

    Proportion of post-quality human reads classified to the following categories:

    .human.untargeted

    Human untargeted

    .human.untargetedSubcategories

    Proportion of post-quality human untargeted reads classified to the following sub-categories:

    .human.untargetedSubcategories.ribosomalDna

    Human ribosomal DNA

    .human.untargetedSubcategories.codingSequence

    Human coding sequence

    .human.untargetedSubcategories.other

    Human other (not ribosomal DNA or coding sequence)

    .internalControl

    Proportion of post-quality Internal Control reads classified to the following categories:

    .internalControl.targeted

    Internal Control targeted

    .internalControl.untargeted

    Internal Control untargeted

    .microbialAndInternalControl

    Proportion of post-quality Microbial and Internal Control reads classified to the following categories:

    .microbialAndInternalControl.targeted

    Microbial and Internal Control targeted

    .microbialAndInternalControl.untargeted

    Microbial and Internal Control untargeted

    .bacterialAmr

    Proportion of post-quality bacterial AMR reads classified to the following categories:

    .bacterialAmr.targeted

    Bacterial AMR targeted

    .bacterialAmr.untargeted

    Bacterial AMR untargeted

    .belowThresholdEnabled*

    Boolean indicating if microorganisms and/or AMR markers below detection thresholds are reported

    .bacterialAmrMarkersOnly*

    (RPIP, UPIP only) Boolean indicating if only bacterial AMR markers are reported

    .bacterialAmrMarkerMicroorganismRequired*

    (RPIP, UPIP only) Boolean indicating if bacterial AMR markers are reported only when an associated microorganism is reported

    .preDefinedMicroorganismReportingList*

    (RPIP, UPIP only) Pre-defined microorganism reporting list, if specified

    .userDefinedMicroorganismReportingListUsed*

    Boolean indicating if a user-defined microorganism reporting file is specified

    .userDefinedMicroorganismReportingListFile*

    Name of the user-defined microorganism reporting file, if specified

    .providedAnalysisName*

    User-provided analysis name

    .rpkm

    Normalized representation of the number of sample sequencing reads aligned to targeted microorganism reference sequences (targeted Reads mapped Per Kilobase of targeted sequence per Million quality-filtered reads)

    .alignedReadCount

    Number of sample sequencing reads that aligned to targeted microorganism reference sequences

    .kmerReadCount

    (UPIP only) Number of sample sequencing reads classified to targeted microorganism reference sequences

    .absoluteQuantityRatio

    Numerical absolute quantification value. Quantitative internal control required for calculation

    .absoluteQuantityRatioFormatted

    Formatted absolute quantification value with units. Quantitative internal control required for calculation

    .phenotypicGroup

    (RPIP, UPIP only) Grouping indicating general association with normal flora, colonization, or contamination from the environment or other sources, as well as general association with disease

    .associatedAmrMarkers

    (Bacteria only) Information about the bacterial AMR markers associated with the microorganism

    .associatedAmrMarkers.applicable

    Boolean indicating whether one or more bacterial AMR markers are associated with the microorganism

    .associatedAmrMarkers.detected

    List of detected bacterial AMR markers associated with the microorganism

    .associatedAmrMarkers.predicted

    List of predicted bacterial AMR markers associated with the microorganism

    .consensusGenomeSequences

    (RPIP, RVOP/RVEK, VSP, VSP V2 viruses only) Information about the majority consensus genome (or segment) sequence

    .consensusGenomeSequences.sequence

    Consensus genome (or segment) sequence bases

    .consensusGenomeSequences.referenceAccession

    Accession of the reference genome (or segment) sequence

    .consensusGenomeSequences.referenceDescription

    Description of the reference genome (or segment) sequence

    .consensusGenomeSequences.referenceLength

    Length of the reference genome (or segment) sequence

    .consensusGenomeSequences.maximumAlignmentLength

    Longest contiguous alignment between consensus sequence and reference genome (or segment) sequence

    .consensusGenomeSequences.maximumGapLength

    Longest contiguous alignment gap (insertion or deletion) between consensus sequence and reference genome (or segment) sequence

    .consensusGenomeSequences.maximumUnalignedLength

    Longest section of the reference genome (or segment) sequence not aligned to by consensus sequence

    .consensusGenomeSequences.coverage

    Proportion of reference genome (or segment) sequence bases that appear in sample sequencing reads

    .consensusGenomeSequences.ani

    Average nucleotide identity of consensus sequence to reference genome (or segment) sequence

    .consensusGenomeSequences.alignedReadCount

    Number of sample sequencing reads that aligned to reference genome (or segment) sequence

    .consensusGenomeSequences.medianDepth

    Median depth of sample sequencing reads aligned to reference genome (or segment) sequence, indicating the median number of times each reference genome (or segment) sequence base appears in sample sequencing reads

    .consensusGenomeSequences.targetAnnotation

    List of targeted region annotations for the reference genome (or segment) sequence. Each annotation is a JSON object with the following fields: start (int), end (int), strand (string: "+", "-"), target_name (string), type (string)

    .consensusGenomeSequences.condensedDepthVector

    Read depth across the reference genome (or segment) sequence, condensed to 256 bins

    .consensusTargetSequences

    (RPIP viruses only) Information about the majority targeted region consensus sequences

    .consensusTargetSequences.sequence

    Consensus targeted region sequence bases

    .consensusTargetSequences.name

    Name of the targeted region

    .consensusTargetSequences.referenceAccession

    Accession of the targeted region reference sequence

    .consensusTargetSequences.depthVector

    Read depth across the targeted region reference sequence, not condensed

    .consensusTargetSequences.scaledDepthVector*

    Read depth across the targeted region reference sequence, condensed and scaled such that the longest targeted region for the microorganism has a maximum length of 256 bins

    .predictionInformation

    Information about microorganism prediction results

    .predictionInformation.predictedPresent

    Boolean indicating whether the microorganism passed its reporting logic algorithm

    .predictionInformation.notes

    List of notes about the prediction result

    .predictionInformation.subpanels

    List of pre-defined subpanels that the microorganism belongs to

    .predictionInformation.relatedMicroorganisms

    Array of objects with information about genetically related microorganisms. See below for details

    .predictionInformation.userDefined*

    User-defined reporting prediction logic for microorganism, if specified

    .variants

    (all RVOP/RVEK, VSP, and VSP V2 viruses, RPIP: SARS-CoV-2 & FluA/B/C only) Information about viral variants. See below for details

    .comments*

    List of additional information regarding the microorganism

    .abundance*

    Relative abundance of the microorganism within the microorganism class

    .pangoLineage*

    (SARS-CoV-2 only) Information about SARS-CoV-2 Pango lineage prediction results. See below for details

    .nextclade*

    (applicable viruses only) Information about viral clade assignment results. See below for details

    .potentialAmrDetected*

    (Bacteria only) Potential AMR detection flag for microorganism. Can be "Yes", “Not Detected”, or “n/a”

    .potentialAmrPredicted*

    (Bacteria only) Potential AMR prediction flag for microorganism. Can be "Yes", “Not Predicted”, or “n/a”

    .flags*

    (Bacteria only) Flag for potential resistance to an important drug class ("Potential ESBL", "Potential Carbapenemase")

    .intrinsicResistance*

    (Bacteria only) List of antimicrobials to which the reported bacteria is intrinsically resistant, based on CLSI Performance Standards for Antimicrobial Susceptibility Testing, M100 34th Edition, Appendix B

    .intrinsicResistanceDrugClasses*

    (Bacteria only) List of drug classes to which the reported bacteria is intrinsically resistant, based on CLSI Performance Standards for Antimicrobial Susceptibility Testing, M100 34th Edition, Appendix B

    .depth

    Variant depth, indicating the number of times variant position appears in sample sequencing reads

    .alleleFrequency

    Frequency of variant allele in sample sequencing reads

    .category*

    Variant category ("Viral Variant; Known AMR", "Viral Variant")

    .comments*

    List of additional information regarding the variant

    .gene*

    (SARS-CoV-2, Flu A/B/C only) Gene name

    .product*

    Protein product of gene

    .annotation*

    Type of change (e.g., "Nonsynonymous Variant")

    .aachange*

    Amino acid change associated with variant

    .epistaticGroups*

    List of epistatic groups variant is associated with

    .standardNomenclatureEpistaticGroups*

    (Flu A/B only) List of epistatic groups variant is associated with using standard nomenclature coordinates

    .standardNomenclatureAaChange*

    (Flu A/B only) Amino acid change associated with variant using standard nomenclature coordinates

    .standardNomenclatureAccession*

    (Flu A/B only) NCBI accession of the reference sequence used to establish standard nomenclature coordinates

    .drugClasses*

    List of drug classes variant is predicted to confer resistance to

    .representativeAntimicrobials*

    List of representative antimicrobials variant is predicted to confer resistance to

    .inhibitionLevel*

    (Flu A/B only) Level of inhibition per cited publications (see pmids)

    .pmids*

    PubMed IDs of publications associated with variant

    Total number of detected nucleotide substitutions

    .totalNonACGTNs*

    Total number of detected ambiguous nucleotides (nucleotide characters that are not A, C, G, T, N)

    .totalMissing*

    Total number of detected missing nucleotides (nucleotide character N)

    .coverage*

    Proportion of consensus genome (or segment) sequence bases that aligned to reference accession

    .totalInsertions*

    Total number of inserted nucleotide bases

    .totalFrameShifts*

    Total number of detected frame shifts

    .stopCodons*

    Total number of detected stop codons

    .version*

    Version of the Nextclade software

    .referenceAccession

    Accession of the bacterial AMR marker reference sequence

    .coverage

    Proportion of bacterial AMR marker reference sequence residues that appear in sample sequencing reads (protein alignment for "homolog" and "protein variant" model types; nucleotide alignment for "rRNA variant" model type)

    .pid

    Percent identity of consensus sequence aligned to bacterial AMR marker reference sequence (protein alignment for "homolog" and "protein variant" model types; nucleotide alignment for "rRNA variant" model type)

    .medianDepth

    Median depth of sample sequencing reads aligned to bacterial AMR marker reference sequence, indicating the median number of times each bacterial AMR marker sequence residue appears in sample sequencing reads (protein alignment for "homolog" and "protein variant" model types; nucleotide alignment for "rRNA variant" model type)

    .rpkm

    Normalized representation of the number of sample sequencing reads aligned to bacterial AMR reference sequence (protein alignment for "homolog" and "protein variant" model types; nucleotide alignment for "rRNA variant" model type)

    .alignedReadCount

    Number of sample sequencing reads that aligned to bacterial AMR reference sequence (protein alignment for "homolog" and "protein variant" model types; nucleotide alignment for "rRNA variant" model type)

    .nucleotideConsensusSequence

    Nucleotide consensus sequence bases

    .proteinConsensusSequence

    Protein consensus sequence bases

    .nucleotideDepthVector

    Read depth across the bacterial AMR marker nucleotide reference sequence, not condensed

    .proteinDepthVector

    Read depth across the bacterial AMR marker protein reference sequence, not condensed

    .associatedMicroorganisms

    Information about the microorganisms associated with the bacterial AMR marker

    .associatedMicroorganisms.all

    List of all microorganisms associated with the bacterial AMR marker

    .associatedMicroorganisms.detected

    List of detected microorganisms associated with the bacterial AMR marker

    .associatedMicroorganisms.predicted

    List of predicted microorganisms associated with the bacterial AMR marker

    .predictionInformation

    Information about bacterial AMR marker prediction results

    .predictionInformation.predictedPresent

    Boolean indicating whether the bacterial AMR marker passed its reporting logic algorithm

    .predictionInformation.confidence

    Confidence level of bacterial AMR marker prediction ("high", "medium", "low")

    .predictionInformation.notes

    List of notes about the prediction result

    .flags*

    Flag indicating AMR marker is an extended-spectrum beta-lactamase (ESBL) or carbapenemase (Carbapenemase)

    .representativeAntimicrobials*

    List of representative antimicrobials the AMR marker is predicted to confer resistance to

    .drugClasses*

    List of drug classes the AMR marker is predicted to confer resistance to

    .referenceAllele

    Reference allele at variant position

    .variantAllele

    Variant allele

    .depth

    Variant depth, indicating the number of times variant position appears in sample sequencing reads

    .alleleFrequency

    Frequency of variant allele in sample sequencing reads

    .annotation

    Type of change (e.g. "Nonsynonymous Variant")

    .aaChange

    Amino acid change associated with variant

    .epistaticGroups

    List of epistatic groups variant is associated with

    .representativeAntimicrobials*

    List of representative antimicrobials variant is predicted to confer resistance to

    .drugClasses*

    List of drug classes variant is predicted to confer resistance to

    .confidenceLevel*

    (MTB only) Confidence level is given for Mycobacterium tuberculosis variants if provided by the WHO Catalogue of mutations in Mycobacterium tuberculosis (Final Grading Confidence; for rpoB only), or the Comprehensive Antibiotic Resistance Database (CARD), as part of a confidence model for AMR developed by the Relational Sequencing Tuberculosis Data Platform (ReSeqTB)

    .pmids*

    PubMed IDs of publications associated with variant

    .alignedReadCount

    Number of sample sequencing reads that aligned to custom reference sequence or, if specified, collection of one or more custom reference sequences

    .consensusSequences

    Array of objects with information about each consensus sequence. See below for details

    .variants

    Array of objects with information about variants detected in custom reference sequence or, if specified, collection of one or more custom reference sequences. See below for details

    .pangoLineage*

    Array of objects with information about SARS-CoV-2 Pango lineage prediction results. See below for details

    .medianDepth

    Median depth of sample sequencing reads aligned to custom reference sequence, indicating the median number of times each custom reference sequence base appears in sample sequencing reads

    .depthVector

    Read depth across custom reference sequence, not condensed

    .alignedReadCount

    Number of sample sequencing reads that aligned to custom reference sequence

    .maximumAlignmentLength

    Longest contiguous alignment between consensus sequence and custom reference sequence

    .maximumGapLength

    Longest contiguous alignment gap (insertion or deletion) between consensus sequence and custom reference sequence

    .maximumUnalignedLength

    Longest section of custom reference sequence not aligned to by consensus sequence

    .alleleFrequency

    Frequency of variant allele in sample sequencing reads

    .accession

    Identifier used for the sample

    .deploymentEnvironment

    Environment in which the results were produced

    .batchId

    Identifier used for the batch of samples processed together

    .analysisId

    Identifier used for the analysis

    .runId

    Identifier used for the sequencing run

    .controlFlag

    Indicates whether the sample is a control. It is set to “POS” if the substring “PosCon” is found in the sample name, “NEG” if the substring “NegCon” is found, or “BLANK” if the substring “controlBlk” is found. Otherwise, it is set to “-”

    .dragenVersion

    DRAGEN release version

    .analysisPipelineVersion

    Analysis Pipeline release version

    .testType

    Type of test panel ("RPIP", "UPIP", "RVOP", "VSPv1", "VSPv2", "Custom")

    .testVersion

    Test panel release version

    .testName

    Full name of test panel

    .testUse

    Test use. "For Research Use Only. Not for use in diagnostic procedures"

    .reportTime

    Date and time the report was generated

    .warnings

    List of warnings encountered during the analysis

    .errors

    List of errors encountered during the analysis

    .results*

    High level result: “One or more potential pathogens predicted” or ”No potential pathogens predicted”

    .appVersion*

    DRAGEN Microbial Enrichment plus application release version

    .totalRawBases

    Number of base pairs in sample before read QC processing

    .totalRawReads

    Number of reads in sample before read QC processing

    .uniqueReads

    Number of distinct reads in sample before read QC processing

    .uniqueReadsProportion

    Proportion of distinct reads in sample before read QC processing

    .preQualityMeanReadLength

    Average read length before read QC processing

    .postQualityMeanReadLength

    Average read length after read QC processing

    .value

    Enrichment factor value reflecting how well targeted regions were enriched

    .category

    Enrichment factor category: "poor", "fair", "good", or "not calculated"

    .readClassification

    Proportion of post-quality reads classified to the following categories:

    .readClassification.targetedMicrobial

    Targeted microbial

    .readClassification.targetedInternalControl

    Targeted Internal Control

    .readClassification.untargeted

    Untargeted

    .readClassification.ambiguous

    More than one category

    .readClassification.unclassified

    No category

    .quantitativeInternalControlName

    Quantitative Internal Control used for microorganism absolute quantification (recommendation: Enterobacteria phage T7)

    .quantitativeInternalControlConcentration

    Quantitative Internal Control concentration (recommendation: 1.21 x 10^7 copies/mL of sample)

    .readQcEnabled

    Boolean indicating if read QC (trimming and filtering based on quality and read length) is enabled

    .readClassificationSensitivity

    (RVOP/RVEK, VSP, VSP V2 only) Sensitivity threshold for classifying reads. Determines whether alignment should proceed for a microorganism and/or reference sequence. Value is an integer with a valid range of 1 to 1000, inclusive

    .customPanelFastaFile

    (Custom Panel only) Name of the custom reference FASTA file

    .customPanelBedFile

    (Custom Panel only) Name of the custom reference BED file

    .class

    Microorganism class ("viral", "bacterial", "fungal", "parasite")

    .name

    Name of microorganism

    .coverage

    Proportion of targeted microorganism reference sequence bases that appear in sample sequencing reads

    .ani

    Average nucleotide identity of consensus sequence to targeted microorganism reference sequences

    .medianDepth

    Median depth of sample sequencing reads aligned to targeted microorganism reference sequences, indicating the median number of times each targeted microorganism reference sequence base appears in sample sequencing reads

    .condensedDepthVector

    Read depth across the targeted microorganism reference sequences, condensed to 256 bins

    .name

    Name of related microorganism

    .onPanel

    Boolean indicating whether the related microorganism is a panel member

    .kmerReadCount

    (UPIP only) Number of sample sequencing reads classified to related microorganism reference sequences

    .coverage

    Proportion of related microorganism reference sequence bases that appear in sample sequencing reads

    .ani

    Average nucleotide identity of consensus sequence to related microorganism reference sequences

    .alignedReadCount

    Number of sample sequencing reads that aligned to related microorganism reference sequences

    .referenceAccession

    Accession of reference genome (or segment) sequence used for variant calling

    .segment

    (Segmented viruses only) Segment number of reference segment sequence

    .ntChange

    Nucleotide change associated with variant

    .referencePosition

    Variant position in viral reference genome (or segment) sequence

    .referenceAllele

    Reference allele at variant position

    .variantAllele

    Variant allele

    Field

    Description [Source]arrow-up-right

    .lineage*

    From Pangolin: "The most likely lineage assigned to a given sequence based on the inference engine used and the SARS-CoV-2 diversity designated. This assignment may be sensitive to missing data at key sites"

    .conflict*

    From Pangolin: "In the pangoLEARN model, a given sequence gets assigned to the most likely category based on known diversity. If a sequence can fit into more than one category, the conflict score will be greater than 0 and reflect the number of categories the sequence could fit into. If the conflict score is 0, this means that within the current decision tree there is only one category that the sequence could be assigned to"

    .ambiguityScore*

    From Pangolin: "This score is a function of the quantity of missing data in a sequence. It represents the proportion of relevant sites in a sequnece which were imputed to the reference values. A score of 1 indicates that no sites were imputed, while a score of 0 indicates that more sites were imputed than were not imputed. This score only includes sites which are used by the decision tree to classify a sequence"

    .version*

    Version of the PUSHER database

    .pangolinVersion*

    Version of the Pangolin software

    Field

    Description [Source]arrow-up-right

    .sequenceName*

    Name of the sequence

    .referenceAccession*

    Reference accession

    .overallStatus*

    Overall quality controlarrow-up-right status

    .clade*

    Assigned clade

    .pangoLineage*

    Pango lineage assigned by Nextclade

    .cladeWho*

    World Health Organization (WHO) nomenclature

    .class

    Microorganism class ("bacterial")

    .cardModelType

    Bacterial AMR marker model type in the Comprehensive Antibiotic Resistance Database (CARD) ("homolog", "protein variant", "rRNA variant")

    .cardGeneFamily

    Bacterial AMR marker gene family in the Comprehensive Antibiotic Resistance Database (CARD)

    .name

    Bacterial AMR marker name

    .cardName

    Bacterial AMR marker name in the Comprehensive Antibiotic Resistance Database (CARD)

    .ncbiName

    Bacterial AMR marker name in the National Center for Biotechnology Information (NCBI) Reference Gene Catalog

    .category

    Variant category ("Bacterial Variant; Known AMR")

    .referenceSourceMicroorganism

    Microorganism that reference sequence is associated with in NCBI

    .comments

    List of additional information regarding the variant

    .product

    Protein product of gene

    .ntChange

    Nucleotide change associated with variant

    .referencePosition

    Variant position in reference sequence

    .name

    Provided name of custom reference sequence, accession, genome, or microorganism

    .coverage

    Proportion of custom reference sequence bases that appear in sample sequencing reads

    .ani

    Average nucleolotide identity of consensus sequence to custom reference sequence or, if specified, collection of one or more custom reference sequences

    .medianDepth

    Median depth of sample sequencing reads aligned to custom reference sequence or, if specified, collection of one or more custom reference sequences, indicating the med\ian number of times each custom reference sequence base appears in sample sequencing reads

    .condensedDepthVector

    Read depth across custom reference sequence or, if specified, collection of one or more custom reference sequences, condensed to 256 bins

    .rpkm

    Normalized number of sample sequencing reads aligned to custom reference sequence or, if specified, collection of one or more custom reference sequences (targeted Reads mapped Per Kilobase of targeted sequence per Million quality-filtered reads)

    .sequence

    Majority consensus sequence bases

    .referenceAccession

    Accession of custom reference sequence

    .referenceDescription

    Description of custom reference sequence

    .referenceLength

    Length of custom reference sequence

    .coverage

    Proportion of custom reference sequence bases that appear in sample sequencing reads

    .ani

    Average nucleolotide identity of consensus sequence to custom reference sequence

    .ntChange

    Nucleotide change associated with variant

    .referenceAccession

    Accession of custom reference sequence used for variant calling

    .referencePosition

    Variant position in custom reference sequence

    .referenceAllele

    Reference allele at variant position

    .variantAllele

    Variant allele

    .depth

    Variant depth, indicating the number of times variant position appears in sample sequencing reads

    Field

    Description [Source]arrow-up-right

    .lineage*

    The most likely lineage assigned to a given sequence based on the inference engine used and the SARS-CoV-2 diversity designated. This assignment may be is sensitive to missing data at key sites

    .conflict*

    In the pangoLEARN model, a given sequence gets assigned to the most likely category based on known diversity. If a sequence can fit into more than one category, the conflict score will be greater than 0 and reflect the number of categories the sequence could fit into. If the conflict score is 0, this means that within the current decision tree there is only one category that the sequence could be assigned to

    .ambiguityScore*

    This score is a function of the quantity of missing data in a sequence. It represents the proportion of relevant sites in a sequnece which were imputed to the reference values. A score of 1 indicates that no sites were imputed, while a score of 0 indicates that more sites were imputed than were not imputed. This score only includes sites which are used by the decision tree to classify a sequence

    .version*

    Version of the PUSHER database

    .pangolinVersion*

    Version of the Pangolin software

    .abbreviations*

    Information about abbreviations relevant to test

    .abbreviations.abbreviation*

    Abbreviation

    .abbreviations.definition*

    Abbreviation definition

    .interpretiveData*

    Information about test

    .interpretiveData.header*

    Test information category

    .interpretiveData.paragraph*

    Test information text

    .substitutions*

    [
        {
            "name": "Allobacillus halotolerans",
            "rpkm": 0
        },
        {
            "name": "Armored RNA Quant Internal Process Control",
            "rpkm": 0
        },
        {
            "name": "Enterobacteria phage T7",
            "rpkm": 180323
        },
        {
            "name": "Escherichia virus MS2",
            "rpkm": 0
        },
        {
            "name": "Escherichia virus Qbeta",
            "rpkm": 0
        },
        {
            "name": "Escherichia virus T4",
            "rpkm": 0
        },
        {
            "name": "Imtechella halotolerans",
            "rpkm": 0
        },
        {
            "name": "Phocid alphaherpesvirus 1",
            "rpkm": 0
        },
        {
            "name": "Phocine morbillivirus",
            "rpkm": 0
        },
        {
            "name": "Truepera radiovictrix",
            "rpkm": 0
        }
    ]