Class picard.cmdline.PicardCommandLineTest

1

tests

0

failures

0

ignored

0.035s

duration

100%

successful

Tests

Test Duration Result
TestPicardPublic 0.035s passed

Standard error

?[1m?[31mUSAGE: PicardCommandLine ?[32m<program name>?[1m?[31m [-h]

?[0m?[1m?[31mAvailable Programs:
?[0m?[37m--------------------------------------------------------------------------------------
?[0m?[31mAlpha Tools:                                     Tools that are currently UNSUPPORTED until further testing and maturation.?[0m
?[32m    CheckFingerprint                             ?[36mComputes a fingerprint from the supplied SAM/BAM file and compares it to the provided genotypes?[0m
?[32m    CollectIndependentReplicateMetrics           ?[36mEstimates the rate of independent replication of reads within a bam.?[0m
?[32m    CollectWgsMetricsWithNonZeroCoverage         ?[36mCollect metrics about coverage and performance of whole genome sequencing (WGS) experiments.  ?[0m
?[32m    CrosscheckReadGroupFingerprints              ?[36mChecks if all read groups appear to come from the same individual?[0m

?[37m--------------------------------------------------------------------------------------
?[0m?[31mFasta:                                           Tools for manipulating FASTA, or related data.?[0m
?[32m    CreateSequenceDictionary                     ?[36mCreates a sequence dictionary for a reference sequence.  ?[0m
?[32m    ExtractSequences                             ?[36mSubsets intervals from a reference sequence to a new FASTA file.?[0m
?[32m    NonNFastaSize                                ?[36mCounts the number of non-N bases in a fasta file.?[0m
?[32m    NormalizeFasta                               ?[36mNormalizes lines of sequence in a FASTA file to be of the same length.?[0m

?[37m--------------------------------------------------------------------------------------
?[0m?[31mIllumina Tools:                                  Tools for manipulating data specific to Illumina sequencers.?[0m
?[32m    CheckIlluminaDirectory                       ?[36mAsserts the validity for specified Illumina basecalling data.  ?[0m
?[32m    CollectIlluminaBasecallingMetrics            ?[36mCollects Illumina Basecalling metrics for a sequencing run.  ?[0m
?[32m    CollectIlluminaLaneMetrics                   ?[36mCollects Illumina lane metrics for the given BaseCalling analysis directory.  ?[0m
?[32m    ExtractIlluminaBarcodes                      ?[36mTool determines the barcode for each read in an Illumina lane.  ?[0m
?[32m    IlluminaBasecallsToFastq                     ?[36mGenerate FASTQ file(s) from Illumina basecall read data.  ?[0m
?[32m    IlluminaBasecallsToSam                       ?[36mTransforms raw Illumina sequencing data into an unmapped SAM or BAM file.?[0m
?[32m    MarkIlluminaAdapters                         ?[36mReads a SAM or BAM file and rewrites it with new adapter-trimming tags.  ?[0m

?[37m--------------------------------------------------------------------------------------
?[0m?[31mInterval Tools:                                  Tools for manipulating Picard interval lists.?[0m
?[32m    BedToIntervalList                            ?[36mConverts a BED file to a Picard Interval List.  ?[0m
?[32m    IntervalListToBed                            ?[36mConverts an Picard IntervalList file to a BED file.?[0m
?[32m    IntervalListTools                            ?[36mManipulates interval lists.  ?[0m
?[32m    LiftOverIntervalList                         ?[36mLifts over an interval list from one reference build to another.  ?[0m
?[32m    ScatterIntervalsByNs                         ?[36mWrites an interval list based on splitting a reference by Ns.  ?[0m

?[37m--------------------------------------------------------------------------------------
?[0m?[31mMetrics:                                         Tools for reporting metrics on various data types.?[0m
?[32m    CalculateHsMetrics                           ?[36mDEPRECATED: Use CollectHsMetrics instead.?[0m
?[32m    CollectAlignmentSummaryMetrics               ?[36m<b>Produces a summary of alignment metrics from a SAM or BAM file.</b>  ?[0m
?[32m    CollectBaseDistributionByCycle               ?[36mChart the nucleotide distribution per cycle in a SAM or BAM file?[0m
?[32m    CollectGcBiasMetrics                         ?[36mCollect metrics regarding GC bias. ?[0m
?[32m    CollectHiSeqXPfFailMetrics                   ?[36mClassify PF-Failing reads in a HiSeqX Illumina Basecalling directory into various categories.?[0m
?[32m    CollectHsMetrics                             ?[36mCollects hybrid-selection (HS) metrics for a SAM or BAM file.  ?[0m
?[32m    CollectInsertSizeMetrics                     ?[36mCollect metrics about the insert size distribution of a paired-end library.?[0m
?[32m    CollectJumpingLibraryMetrics                 ?[36mCollect jumping library metrics. ?[0m
?[32m    CollectMultipleMetrics                       ?[36mCollect multiple classes of metrics.  ?[0m
?[32m    CollectOxoGMetrics                           ?[36mCollect metrics to assess oxidative artifacts.?[0m
?[32m    CollectQualityYieldMetrics                   ?[36mCollect metrics about reads that pass quality thresholds and Illumina-specific filters.  ?[0m
?[32m    CollectRawWgsMetrics                         ?[36mCollect whole genome sequencing-related metrics.  ?[0m
?[32m    CollectRnaSeqMetrics                         ?[36mProduces RNA alignment metrics for a SAM or BAM file.  ?[0m
?[32m    CollectRrbsMetrics                           ?[36m<b>Collects metrics from reduced representation bisulfite sequencing (Rrbs) data.</b>  ?[0m
?[32m    CollectSequencingArtifactMetrics             ?[36mCollect metrics to quantify single-base sequencing artifacts.  ?[0m
?[32m    CollectTargetedPcrMetrics                    ?[36mCalculate PCR-related metrics from targeted sequencing data. ?[0m
?[32m    CollectVariantCallingMetrics                 ?[36mCollects per-sample and aggregate (spanning all samples) metrics from the provided VCF file?[0m
?[32m    CollectWgsMetrics                            ?[36mCollect metrics about coverage and performance of whole genome sequencing (WGS) experiments.?[0m
?[32m    CollectWgsMetricsFromQuerySorted             ?[36mWrites sequencing-related metrics for a SAM or BAM file?[0m
?[32m    CollectWgsMetricsFromSampledSites            ?[36mWrites whole genome sequencing-related metrics for a SAM or BAM file?[0m
?[32m    CompareMetrics                               ?[36mCompare two metrics files.?[0m
?[32m    ConvertSequencingArtifactToOxoG              ?[36mExtract OxoG metrics from generalized artifacts metrics.  ?[0m
?[32m    EstimateLibraryComplexity                    ?[36mEstimates the numbers of unique molecules in a sequencing library.  ?[0m
?[32m    MeanQualityByCycle                           ?[36mCollect mean quality by cycle.?[0m
?[32m    QualityScoreDistribution                     ?[36mChart the distribution of quality scores.  ?[0m

?[37m--------------------------------------------------------------------------------------
?[0m?[31mMiscellaneous Tools:                             A set of miscellaneous tools.                ?[0m
?[32m    BaitDesigner                                 ?[36m<b>Designs oligonucleotide baits for hybrid selection reactions.</b>  ?[0m
?[32m    FifoBuffer                                   ?[36mFIFO buffer used to buffer input and output streams with a customizable buffer size ?[0m

?[37m--------------------------------------------------------------------------------------
?[0m?[31mSAM/BAM:                                         Tools for manipulating SAM, BAM, or related data.?[0m
?[32m    AddCommentsToBam                             ?[36mAdds comments to the header of a BAM file.?[0m
?[32m    AddOrReplaceReadGroups                       ?[36mReplace read groups in a BAM file.?[0m
?[32m    BamIndexStats                                ?[36mGenerate index statistics from a BAM file?[0m
?[32m    BamToBfq                                     ?[36mCreate BFQ files from a BAM file for use by the maq aligner.  ?[0m
?[32m    BuildBamIndex                                ?[36mGenerates a BAM index ".bai" file.  ?[0m
?[32m    CalculateReadGroupChecksum                   ?[36mCreates a hash code based on the read groups (RG).  ?[0m
?[32m    CheckTerminatorBlock                         ?[36mAsserts the provided gzip file's (e.g., BAM) last block is well-formed; RC 100 otherwise?[0m
?[32m    CleanSam                                     ?[36mCleans the provided SAM/BAM, soft-clipping beyond-end-of-reference alignments and setting MAPQ to 0 for unmapped reads?[0m
?[32m    CompareSAMs                                  ?[36mCompare two input ".sam" or ".bam" files.  ?[0m
?[32m    DownsampleSam                                ?[36mDownsample a SAM or BAM file.  ?[0m
?[32m    FastqToSam                                   ?[36mConverts a FASTQ file to an unaligned BAM or SAM file.  ?[0m
?[32m    FilterSamReads                               ?[36mSubset read data from a SAM or BAM file?[0m
?[32m    FixMateInformation                           ?[36mVerify mate-pair information between mates and fix if needed.?[0m
?[32m    GatherBamFiles                               ?[36mConcatenate one or more BAM files as efficiently as possible?[0m
?[32m    MarkDuplicates                               ?[36mIdentifies duplicate reads.  ?[0m
?[32m    MarkDuplicatesWithMateCigar                  ?[36mIdentifies duplicate reads, accounting for mate CIGAR.  ?[0m
?[32m    MergeBamAlignment                            ?[36mMerge alignment data from a SAM or BAM with data in an unmapped BAM file.  ?[0m
?[32m    MergeSamFiles                                ?[36mMerges multiple SAM and/or BAM files into a single file.  ?[0m
?[32m    PositionBasedDownsampleSam                   ?[36mDownsample a SAM or BAM file to retain a subset of the reads based on the reads location in each tile in the flowcell.?[0m
?[32m    ReorderSam                                   ?[36mReorders reads in a SAM or BAM file to match ordering in reference?[0m
?[32m    ReplaceSamHeader                             ?[36mReplaces the SAMFileHeader in a SAM or BAM file.  ?[0m
?[32m    RevertOriginalBaseQualitiesAndAddMateCigar   ?[36mReverts the original base qualities and adds the mate cigar tag to read-group BAMs?[0m
?[32m    RevertSam                                    ?[36mReverts SAM or BAM files to a previous state.  ?[0m
?[32m    SamFormatConverter                           ?[36mConvert a BAM file to a SAM file, or a SAM to a BAM?[0m
?[32m    SamToFastq                                   ?[36mConverts a SAM or BAM file to FASTQ.  ?[0m
?[32m    SetNmAndUqTags                               ?[36mFixes the UQ and NM tags in a SAM file.  ?[0m
?[32m    SortSam                                      ?[36mSorts a SAM or BAM file.  ?[0m
?[32m    SplitSamByLibrary                            ?[36mSplits a SAM or BAM file into individual files by library?[0m
?[32m    ValidateSamFile                              ?[36mValidates a SAM or BAM file.  ?[0m
?[32m    ViewSam                                      ?[36mPrints a SAM or BAM file to the screen?[0m

?[37m--------------------------------------------------------------------------------------
?[0m?[31mUnit Testing:                                    Unit testing                                 ?[0m
?[32m    SimpleMarkDuplicatesWithMateCigar            ?[36mExamines aligned records in the supplied SAM or BAM file to locate duplicate molecules.?[0m
?[32m    TestParserFail                               ?[36mThis tool offers.....?[0m
?[32m    TestParserSucceed                            ?[36m X &lt; Y ?[0m

?[37m--------------------------------------------------------------------------------------
?[0m?[31mVCF/BCF:                                         Tools for manipulating VCF, BCF, or related data.?[0m
?[32m    FilterVcf                                    ?[36mHard filters a VCF.?[0m
?[32m    FixVcfHeader                                 ?[36mReplaces or fixes a VCF header.?[0m
?[32m    GatherVcfs                                   ?[36mGathers multiple VCF files from a scatter operation into a single VCF file?[0m
?[32m    GenotypeConcordance                          ?[36mEvaluate genotype concordance between callsets.?[0m
?[32m    LiftoverVcf                                  ?[36mLifts over a VCF file from one reference build to another.  ?[0m
?[32m    MakeSitesOnlyVcf                             ?[36mCreates a VCF bereft of genotype information from an input VCF or BCF?[0m
?[32m    MergeVcfs                                    ?[36mMerges multiple VCF or BCF files into one VCF file or BCF?[0m
?[32m    RenameSampleInVcf                            ?[36mRenames a sample within a VCF or BCF.  ?[0m
?[32m    SortVcf                                      ?[36mSorts one or more VCF files.  ?[0m
?[32m    SplitVcfs                                    ?[36mSplits SNPs and INDELs into separate files.  ?[0m
?[32m    UpdateVcfSequenceDictionary                  ?[36mTakes a VCF and a second file that contains a sequence dictionary and updates the VCF with the new sequence dictionary.?[0m
?[32m    VcfFormatConverter                           ?[36mConverts VCF to BCF or BCF to VCF.  ?[0m
?[32m    VcfToIntervalList                            ?[36mConverts a VCF or BCF file to a Picard Interval List.?[0m

?[37m--------------------------------------------------------------------------------------

?[0m'' is not a valid command. See PicardCommandLine --help for more information.