这里给出 MATLAB_R2017a 的生物信息学工具箱中 自带的样例 一览：
如果是默认安装，则相关目录在：
C:\Program Files\MATLAB\R2017a\examples\bioinfo
按字母排序如下：
AlignMultipleSequencesExample.m
AlignQuerySequenceToProfileUsingHMMModelAlignmentExample.m
AUCNormalizationExample.m
BuildPhylogeneticTreefromPairwiseDistancesExample.m
BuildPhylogeneticTreeusingNeighborJoiningMethodExample.m
CalculateAffymetrixProbeAffinitiesExample.m
CalculateMaximumFlowExample.m
CalculateRangeOfGeneExpressionProfilesExample.m
CalculateSequenceProfilefromPartofAlignmentCountingAllGaExa
CalculateTheAtomicCompositionOfAProteinExample.m
CalculateVarianceOfGeneExpressionProfilesExample.m
ChangeReferenceSequenceOfBioMapObjectExample.m
CharacterizeGenesInvolvedInTheYeastDiauxicShiftExample.m
CleaveASequenceExample.m
ComputeTheNumberOfReadsMappedToRefSeqExample.m
ConstructABioIndexedFileObjectAndAccessItsGOExample.m
ConstructABioMapObjectExample.m
ConstructAnExptDataObjectExample.m
ConstructBioReadObjectfromFASTQFileExample.m
ConstructBioReadObjectfromMATLABStructureExample.m
ConstructBioReadObjectfromMATLABWorkspaceVariablesExample.m
ConvertADNASequenceToAnRNASequenceExample.m
ConvertAlignedSequencesToCIGARStringsExample.m
ConvertAnAminoAcideSequenceToANucleotideSequenceExample.m
ConvertAnAminoAcidSequenceToSingleletterOrThreeletterExampl
ConvertANucleotideSequenceToItsComplementarySequenceExample
ConvertARandomAminoAcidSequenceExample.m
CountAminoAcidsInASequenceExample.m
CountCodonsInANucleotideSequenceExample.m
CountCodonsInNucleotideSeqExample.m
CountDimersInANucleotideSequenceExample.m
CountNucleotidesInASequenceExample.m
CountTheNumberOfReadsMappedToGenomicFeaturesExample.m
CreateABiographObjectAndCalculateNodePositionExample.m
CreateABiographObjectExample.m
CreateABioMapObjectDisplayInNGSBrowserExample.m
CreateAPhylogeneticTreeExample.m
CreateBiographObjSpecifyAccessItsPropsExample.m
CreatePCAPlotOfMicroarrayDataExample.m
CreateQualityControlPlotsForSequenceAndQualityDataExample.m
DetermineImportantFeaturesFromFisherIrisDataExample.m
DisplayASequenceLogoForAlignedAASeqExample.m
DisplayBoxPlotsForMicroarrayDataExample.m
DisplayCNVDataAlginedToChromosomeIdeogramExample.m
DisplaySequenceLogoForNucleotideSeqExample.m
DisplayTheFrequencyOfCNAExample.m
EstimateSynonymousAndNonsynonymousSubRatesExample.m
EstimateSynonymousAndNonsynonymousSubRatesMLExample.m
FilterNextgenerationSequencingDataExample.m
FilterOutGeneswithLowAbsoluteExpressionLevelsExample.m
GenerateAnIndexStructFromBAMFileExample.m
GenerateSpatialImageForMicroarrayDataExample.m
MaximumIntensityNormalizationExample.m
NormalizeAffymetrixDataExample.m
NormalizeMicroarrayDataExample.m
OpenAndViewABiologicalSequenceExample.m
PerformCBSOnCGHDataExample.m
PerformHierarchicalClusteringOnGeneExpressionDataExample.m
PerformUnpairedHypothesisTestForShortreadCountDataExample.m
PlotAHeatmapOfDataMatrixExample.m
PlotASetOfMassSpectraDataExample.m
PlotChromosomeIdeogramsExample.m
QuantileNormalizationExample.m
ReadCytogeneticBandingInformationFromAFileExample.m
ReadDataFromGPRFileExample.m
ReadSequenceDataFromFASTAFilesExample.m
ReadSequenceInformationFromEMBLFileExample.m
ResampleMassSpectrometryDataExample.m
RetrieveAlignmentRecordsThatAlignToTwoRefSeqExample.m
RetrieveBLOSUMScoringMatrixExample.m
RetrieveExonsFromAGTFformattedFileExample.m
RetrieveGenesFromAGTFformattedFileExample.m
RetrieveInfoAboutBAMFileExample.m
RetrieveSegmentsFromAGTFformattedFileExample.m
RetrieveTranscriptsFromAGTFformattedFileExample.m
SendRasMolScriptCommandsToMoleculeViewerAppExample.m
SmoothMassSpectrometryDataExample.m
SplitMergedPairedendSequencesIntoSeparateFilesExample.m
SplitSequencesIntoSeparateFilesBasedOnBarcodesExample.m
TrimSequencesInAFASTQFileExample.m
UpdateSAMFlagValuesOfBioMapObjectExample.m
View3DStructureOfAMoleculeExample.m
ViewAMultipleSequenceAlignmentFileExample.m
ViewAPhylogeneticTreeExample.m
将在 MATLAB生物信息分析工具箱（二） 中简要地介绍每一个文件的用途。