site preparation and training guide v2.1 - amazon s3preparation+and... · omixon holotype hla site...
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HOLOTYPEHLA™SITEPREPARATIONGUIDE
FORRESEARCHUSEONLY
V2.1
OmixonLimited
CONFIDENTIAL&PROPRIETARY.ALLRIGHTSRESERVED.
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OmixonHolotypeHLASitePreparationandTrainingGuidev2.1.Forresearchuseonly.Copyright©2017,OmixonBiocomputingLtd.Confidential&Proprietary Page2│25
TableofContentsRECOMMANDATIONS...........................................................................................................................................3
DNAEXTRACTIONRECOMMANDATIONS............................................................................................................................3TECHNICALANDEQUIPMENTRECOMMENDATIONS..............................................................................................................3ASSOCIATEDREAGENTRECOMMENDATIONS.......................................................................................................................3
MiSeqReagentKitcapacity.................................................................................................................................4RECOMMENDEDSUPPLIES...............................................................................................................................................4
DOCUMENTHISTORY...........................................................................................................................................6LEGALNOTICE......................................................................................................................................................7PROTOCOLOVERVIEW(24/7CONFIGURATION)...................................................................................................8AMPLIFICATIONSUMMARY..................................................................................................................................9
ExpectedAmpliconSizes......................................................................................................................................9STEP0–GENOMICDNAPREPARATION..............................................................................................................10STEP1–HLAAMPLIFICATIONMASTERMIXPREPARATION................................................................................11STEP2–HLACLASSIANDIIAMPLIFICATION......................................................................................................12
ClassIAmplification(HLA-A,BandC)...............................................................................................................12ClassIIAmplification(HLA-DRB1/3,DRB4,DRB5,DPA1/DPB1,DQA1,DQB1set1andDQB1set2)................12
STEP3–AMPLICONQUANTITATIONANDNORMALIZATION..............................................................................14STEP4–LIBRARYPREPARATION........................................................................................................................16
FragmentationProgram....................................................................................................................................16EndRepairProgram...........................................................................................................................................16LigationProgram...............................................................................................................................................16
STEP5–LIBRARYSIZESELECTION.......................................................................................................................18STEP6–LIBRARYQUANTIFICATION...................................................................................................................19STEP7–SEQUENCINGONILLUMINAMISEQ......................................................................................................20STEP8–ANALYSISOFHLASEQUENCINGDATA..................................................................................................21ONSITEANDREMOTETRAINING........................................................................................................................22TECHNICALASSISTANCE.....................................................................................................................................25
PhoneSupport:..................................................................................................................................................25
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Recommandations
DNAExtractionRecommandations§ Genomic DNA (gDNA) extracted from blood, saliva, buccal swabs, and hematopoietic
blood cells (B-cell lines, buffy coats, cord blood or any fraction of white blood cells)sufficientfor150ngofstartinginputforeachlong-rangePCRreaction,a260nm/280nmODratioof1.7-1.9,anda260nm/230nmODratiogreaterthan1.7.Eachsampleshouldrequiretotalinputof0.8-1.2µggDNAfor7lociand1.0-1.5µgofgDNAfor11loci.gDNAshouldbedissolved inwater if possible. EDTA inTEbuffer can inhibit long-rangePCRreactions.
TechnicalandEquipmentRecommendations§ Thermalcyclerwith96-wellformat§ Platefluorometer(oranyinstrumentcapableoffluorescencedetectionin96-wellplate
format,forusewiththePromegaQuantiFluordsDNASystem)§ PippinPrep(Cat#PIP0001)orBluePippin(Cat#BLU0001)bySAGEScience§ Qubitfluorometer(ThermoFisherScientific)§ qPCRinstrumentwith96or384-wellplateformat(optional)§ IlluminaMiSeq(Cat#SY-410-1003)§ 64-bitcomputerwithminimum4Coresand16GBofRAM§ Long-termdatastorage(approximately2TBofdataperMiSeqperyear)
AssociatedReagentRecommendations§ LongRangePCRkitsfromQiagen(Cat#206401,206402or206403)
§ Eachsamplerequires4.4μLofLongRangeenzymefor11loci§ Cat#206401LongRangePCRkit(20)contains8μLofenzyme§ Cat#206402LongRangePCRkit(100)contains40μLofenzyme§ Cat#206403LongRangePCRkit(250)contains100μLofenzyme
§ ExoSAP-IT Express from Affymetrix (Cat# 75001-200, 75001-1ML, 75001-4X-1ML or75001-10ML)
§ Eachpooledsamplerequires4μLofExoSAP-ITExpressenzyme§ Cat#75001-200contains200μLofExoSAP-ITExpressenzyme§ Cat#75001-1MLcontains1mLofExoSAP-ITExpressenzyme§ Cat#75001-4X-1MLcontains4mLofExoSAP-ITExpressenzyme§ Cat#75001-10MLcontains10mLofExoSAP-ITExpressenzyme
§ QubitdsDNABRAssayKit(Cat#Q32850orQ32853)§ Cat#Q32850for100assays§ Cat#Q32853for500assays
§ Library Quantification Kit – Illumina/Universal from KAPA Biosystems (Cat# KK4824) -optionalifusingqPCRforlibraryquantitation
§ QuantiFluordsDNASystemfromPromega(Cat#E2670)
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OmixonHolotypeHLASitePreparationandTrainingGuidev2.1.Forresearchuseonly.Copyright©2017,OmixonBiocomputingLtd.Confidential&Proprietary Page4│25
§ AgencourtAMPureXPbeadsfromBeckmanCoulter(Cat#A63880,A63881,orA63882)§ EachHolotypeHLArunrequiresamaximumof900μLofAMpureXPbeads§ Cat#A63880contains5mLofAMPureXPbeads§ Cat#A63881contains60mLofAMPureXPbeads§ Cat#A63882contains450mLofAMPureXPbeads
§ Gelcassette,1.5%agarose,dyefreewithinternalstandard(MarkerK/R2),forthePippinPrep/BluePippin(Cat#CDF1510forPippinPrepandBDF1510forBluePippin)
§ Moleculargradeethanol(AnhydrousAlcohol)§ Moleculargradewater(DNaseandRNasefree)§ Sodiumhydroxide§ 1×TEbuffer(pH8.0)§ MiSeqReagentKitfromIllumina
MiSeqReagentKitcapacityIlluminaMiSeqReagentKit
TimeHours
24/7Samples
24/11Samples
96/5Samples
96/7Samples
96/11Samples
Std300Cycle(MS-102-2002)
~24 24 24 96 80 72
Micro300Cycle(MS-103-1002)
~19 24 20 40 28 20
Nano300Cycle(MS-103-1001)
~17 6 4 8 6 4
Std500Cycle(MS-102-2003)
~39 24 24 96 96 96
Nano500Cycle(MS-103-1003)
~28 12 8 16 12 8
RecommendedSupplies§ 1.5mLmicrocentrifugetubes§ 1.5mLlow-bindmicrocentrifugetubes§ 2.0mLlow-bindmicrocentrifugetubes(EppendorfDNALoBindCat#022431048
recommended)§ 0.5mlthinwalltubesforQubitinstrument(QubitAssaytubesCat#Q32856
recommended)§ Adjustablevolumepipettes(1.0–1000μLcapacity)§ 8-channeladjustablevolumepipettes(1.0-100μLcapacity)§ 96-wellplatescompatiblewiththethermalcycler§ 96-wellopticalplatescompatiblewiththeplatefluorometer§ 96-wellplatescompatiblewiththeqPCRinstrument(optional)§ Platesealsforgeneraluse§ Platesealscompatiblewiththethermalcyclers(testedforlongrangePCR)§ OpticalplatesealscompatiblewiththeqPCRinstrument(optional)§ Magneticstandcompatiblewith2mLmicrocentrifugetubes§ 96-wellcoolerracks(2pieces)
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§ 50mLconicaltubes§ 50mLreservoirs
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DocumentHistoryVersion Date DescriptionofChanges1.1 January,2015 InitialVersion1.2 March,2015 X2-24/7,X2-96/7added1.3 June,2015 ExoSAP-ITStepChange,AmplificationSummaryadded,
removedX2-96/5andX4-16/51.4 July,2015 1.5 March2016 DPA1,DRB3,DRB4andDRB5locusinformationadded,
Miseqreagentkitcapacitytableadded2.0 January2017 Substitution of ExoSAP-IT with ExoSAP-IT Express,
additionofQubitinstrumentandreagentinformation2.1 November2017 UpdateoflocusconfigurationsandupdateofEndrepair
and Ligation reaction times according to the updatedHolotypeHLAkit
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LegalNoticeThe Holotype HLA User Manual and all contents are proprietary to Omixon Biocomputing("Omixon"), and are intended solely for the contractual useby its customer in regard to theproduct(s)describedhereinandfornootherpurpose.Thisdocumentanditscontentsshallnotbe used or distributed for any other purpose and/or otherwise communicated, disclosed, orreproducedinanywaywhatsoeverwithoutthepriorwrittenconsentofOmixon.Omixondoesnotconveyanylicenseunderitspatent,trademark,copyright,orcommon-lawrightsnorsimilarrightsofanythirdpartiesbythisdocument.UseofOmixonHolotypeorMonotypeHLA(includingsoftwareandassay)isgovernedbyTermsandConditionsGoverningOmixonProducts(www.omixon.com/supply-agreement/),whichreferencestheOmixonHLATwinEULA(www.omixon.com/hla-twin-eula/).
UseofOmixonTargetsoftwareisgovernedbytheOmixonTargetEULA(www.omixon.com/omixon-target-eula/).UseofOmixonHLATwinsoftwarealoneisgovernedbytheOmixonHLATwinEULA(www.omixon.com/hla-twin-eula/).
UseofOmixonHLAExploresoftwareisgovernedbytheOmixonHLAExploreEULA(www.omixon.com/hla-explore-eula/).
The instructions in this document must be strictly and explicitly followed by qualified andproperlytrainedpersonnelinordertoensuretheproperandsafeuseoftheproduct(s)describedherein.Allofthecontentsofthisdocumentmustbefullyreadandunderstoodpriortousingsuchproduct(s).FAILURETOCOMPLETELYREADANDEXPLICITLYFOLLOWALLOFTHEINSTRUCTIONSCONTAINEDHEREINMAY RESULT INDAMAGE TO THE PRODUCT(S), INJURY TO PERSONS, INCLUDING TOUSERSOROTHERS,ANDDAMAGETOOTHERPROPERTY.OMIXON DOES NOT ASSUME ANY LIABILITY ARISING OUT OF THE IMPROPER USE OF THEPRODUCT(S)DESCRIBEDHEREIN(INCLUDINGPARTSTHEREOFORSOFTWARE)ORANYUSEOFSUCHPRODUCT(S)OUTSIDETHESCOPEOFTHEEXPRESSWRITTENLICENSESORPERMISSIONSGRANTEDBYOMIXONINCONNECTIONWITHCUSTOMER'SACQUISITIONOFSUCHPRODUCT(S).FORRESEARCHUSEONLY©2017OmixonBiocomputingLtd.Allrightsreserved.
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ProtocolOverview(24/11configuration)
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AmplificationSummary
ExpectedAmpliconSizes
HLAlocus Expectedampliconsize(kb)HLA-A,BandC ~3HLA-DRB1/3 ~4.3HLA-DRB4 ~4.2HLA-DRB5 ~5HLA-DPA1 ~5.5HLA-DPB1 ~6.6HLA-DQA1 ~5.5
HLA-DQB1(Set3) ~6.5
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Step0–GenomicDNAPreparationDuration:~45minutesTheHolotypeHLAassayisdesignedtoprovideaccuratesequencingdataoftheHLAregionusingtheIlluminaMiSeq.ToachievethebestresultswithHolotypeHLA,itisimportantthathighqualitygenomicDNAisused.DNAcanbe isolatedfromnumeroussources,butat least0.8-1.2µgofgenomic DNA for 7 loci and 1.0-1.5 µg of genomic DNA for 11 loci with a spectroscopicallydetermined260nm/280nmpuritybetween1.7and1.9anda260nm/230nmratiogreaterthan1.7isrequiredforeachsample.TheDNAcanbesetasideuntilthelocusspecificmastermixesarereadyfortheamplificationstep.
Protocol sub-steps § ExtractgDNAfromblood,saliva,buccalswabsorhematopoieticbloodcells(B-celllines,
buffycoats,cordbloodoranyfractionofwhitebloodcells).§ 0.8-1.2µgofinputgenomicDNAwitha260nm/280nmODratiobetween1.7–1.9anda
260nm/230nmratiogreaterthan1.7persampleisrecommended.
Equipment/Supplies § 1.5mLmicrocentrifugetubes§ DeviceformeasuringconcentrationandpurityofgenomicDNA§ Singlechannelmicropipettes§ Vortex§ Microcentrifuge
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Step1–HLAAmplificationMasterMixPreparationDuration:~50minutesOmixonprovidesmostofthereagentsnecessaryforalong-rangePCRreactionintheHolotypeHLAkit,andtheremainingreagentsareincludedwiththeQiagenLong-RangePCRkit.Thelocus-specific mixes contain the necessary primers for amplification. The dNTPs and buffers arecombinedwiththelocusspecificprimers,forminganAmplificationMasterMixforeachlocus.ThecombinedHLAAmplificationMasterMixcanthenbestoreduntiltheactualamplificationisperformed.
Protocol sub-steps § CreateLocus-SpecificMasterMixes
Reagents § HolotypeHLALocus-SpecificPrimermixes§ QiagenLong-RangePCRkit
Equipment/Supplies § Singlechannelmicropipettes§ 1.5mLmicrocentrifugetubes§ Vortex§ Microcentrifuge
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Step2–HLAClassIandIIAmplificationDuration:~6hours45minutesTheHLA Class I and II Amplification takes the genomic DNA and locus-specificmastermixesprepared in earlier steps and begins the process of amplifying the HLA loci. Two separateamplificationconditions,forHLAClassIandIIrespectively,areconcurrentlyrun.Anagarosegelverificationcanbedoneoptionally.
Protocol sub-steps § PCRAmplifications
§ 7reactionspersampleinthe24/7and96/7kits§ 10reactionspersampleinthe24/11and96/11kits
ClassIAmplification(HLA-A,BandC)NumberofCycles Temperature Time
1 95°C 3minutes 95°C 15seconds
35 65°C 30seconds 68°C 5minutes1 68°C 10minutes1 4°C ∞
ClassIIAmplification(HLA-DRB1/3,DRB4,DRB5,DPA1,DPB1,DQA1,DQB1set3)NumberofCycles Temperature Time
1 95°C 3minutes 93°C 15seconds
35 60°C 30seconds 68°C 9minutes1 68°C 10minutes1 4°C ∞
Reagents
HolotypeHLALocus-SpecificPrimerMasterMixesfromStep1
Equipment/Supplies § 96-wellPCRplates§ Singlechannelmicropipettes§ Multichannelmicropipettes§ Thermalseal§ Centrifugefor96-wellPCRplates§ Thermalcyclerswith96-wellplatecapacity
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§ 3xthermalcyclersforthe24/7configuration§ 7xthermalcyclersforthe96/7configuration§ 3xthermalcyclersforthe24/11configuration§ 10xthermalcyclersforthe96/11configuration
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Step3–AmpliconQuantitationandNormalizationDuration:~35minutesOncesampleshavebeensuccessfullyamplified,aninitialdilutionstepisnecessarytohaveanoptimumconcentrationofDNAforlibrarypreparation.TheconcentrationisdeterminedusingastandardplatefluorometerorqPCRmachineandtheQuantiFluordsDNAkitfromPromega.DNAis then diluted, pooled per sample, and then purified using the ExoSAP-IT Express kit fromAffymetrix.ThepooledDNAsamplesarethenreadyforlibrarypreparation.
Protocol sub-steps § Ampliconconsolidation§ AmpliconquantitationwithaplatefluorometerorqPCRmachine§ Amplicondilution§ Ampliconpooling§ Ampliconclean-upusingExoSAP-ITExpress
ExoSAP-ITExpressPCRPurification
Reagents § QuantiFluordsDNASystem§ 1xTEBuffer§ ExoSAP-ITExpress
Equipment/Supplies § Multichannelmicropipettes§ Singlechannelmicropipettes§ 1.5mlmicrocentrifugetubes§ Vortex§ Microcentrifuge§ Centrifugefor96-wellPCRplates§ Pipettingreservoir§ Serologicalpipettes§ 50-mlfalcontubes§ 96-wellopticalbottomplates(forplatefluorometer)§ qPCR96-wellPCRplates(forqPCRmachine)§ Opticalplateseals(forqPCRmachine)§ 96-wellstandardPCRplates
NumberofCycles Temperature Time1 37°C 4minutes1 80°C 1minute1 4°C ∞
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§ Standardplateseals§ Platefluorometer§ qPCRinstrument§ Thermalcyclerswith96-wellplatecapacity
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Step4–LibraryPreparationDuration:~3hours20minutesLibrarypreparationisasequenceofreactionsrunagainstthepooledamplicons.Fragmentationoftheampliconsisimmediatelyfollowedbyendrepair.Theampliconsarethentransferredintoa 96-well plate preloaded with adaptors compatible with the Illumina MiSeq system. Theampliconsandadaptorsarethenligatedtogether.Theligatedfragmentsarepooledtogether,purified,andconcentratedusingAMPureXPbeads.
Protocol sub-steps § Poolingsamplelocitogether§ Enzymaticfragmentationofamplicons§ Endrepairofamplicons§ Ligationofadaptorstotheamplicons§ Poolingoftheadaptorligatedampliconsintoalibrary§ AMPureXPbeadpurificationandconcentrationofthelibrary
FragmentationProgram
NumberofCycles Temperature Time1 37°C 10minutes1 70°C 15minutes1 4°C ∞
EndRepairProgram
NumberofCycles Temperature Time1 20°C 30minutes1 70°C 5minutes1 4°C ∞
LigationProgram
NumberofCycles Temperature Time1 25°C 10minutes1 70°C 10minutes1 4°C ∞
Reagents § HolotypeHLALibraryPreparationReagents§ AMPureXPbeads§ Ethanol
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Equipment/Supplies§ Multichannelmicropipettes§ 96-wellPCRplates§ Thermalseal§ Thermalcycler§ 1.5mLmicrocentrifugetubes§ 1.5mLlow-bindmicrocentrifugetubes§ 2.0mLlow-bindmicrocentrifugetubes§ Vortex§ Microcentrifuge§ Centrifugefor96-wellPCRplates§ Singlechannelmicropipettes§ 2×frozenthermalrackscompatiblewith96-wellPCRplates§ Magnetictuberackforbeadseparation
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Step5–LibrarySizeSelectionDuration:~1hourLibrarypreparationcangeneratenumerousfragmentsofvaryingsizes.ThePippinPrepfromSageScienceefficientlyselectsforfragmentsoftheappropriatesize,eliminatingtheneedforagelexcision and cleanup. The size-selected library can then be prepared for sequencing on theIlluminaMiSeq.
Protocol sub-steps § SizeselectionofthelibraryusingaPippinPreporBluePippin
Reagents § PippinPrepMarkerK(BluePippinMarkerR2)§ PippinPrepElectrophoresisBuffer
Equipment/Supplies§ Singlechannelmicropipettes§ PippinPrepwith1.5%dyefreeagarosecassette§ 1.5mLlow-bindmicrocentrifugetube§ Vortex§ Microcentrifuge
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Step6–LibraryQuantificationDuration:~15minutesThefinalstepbeforerunningthesamplelibraryonanIlluminaMiSeqistodeterminethenumberofampliconssuccessfully ligatedtoadaptors.Theamountof ligatedadaptorsdeterminestheidealdilutionnecessaryforsequencingontheIlluminaMiSeq.Iftheconcentrationofampliconsistoolow,theremaybeallelicdropoutduringMiSeqanalysis.Iftheconcentrationofampliconsistoohigh,therewillbeexcessivenoiseintheMiSeqanalysis.LibraryquantificationcanbedoneusingaQubitandtheQubitBRAssaykit.Alternatively,qPCRwiththeKAPABiosystemsLibraryQuantificationkitcanbeused.
Protocol sub-steps § QubitBRassayreagentpreparation§ Librarydilution§ Qubitquantification
Reagents § QubitBRAssayKit
Equipment/Supplies§ QubitFluorometer§ Singlechannelmicropipettes§ 0.5mLmicrocentrifugetubes
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Step7–SequencingonIlluminaMiSeqDuration:~19hoursTheIlluminaMiSeqhasbeendesignedtoautomatetheprocessofsequencinglargeamountsofDNAinarelativelyshortamountoftime.ThemostcriticalaspectsofoperatinganIlluminaMiSeqareperformingthenecessarywashesandmaintenancetokeepthedevicerunningingoodorder.ThenecessarystepsbeforeloadingyourlibraryontotheMiSeqinvolveaseriesofwashestoflushoutanyremainingcontaminationfromearlierruns,andmakingsurethattheflowcellisascleanaspossible.Once thesestepshavebeendone,a reagentcartridgewith thepreparedsamplelibraryisloadedandafreshlycleanedflowcellisinsertedintothedevice.
Protocol sub-steps § Librarydenaturationanddilution§ IlluminaMiSeqpreparation
Reagents § AnyIlluminaMiSeqReagentKitv2(dependingonsamplevolumeanddesiredTAT–300
cyclekitsrecommended)o 300-CycleNanoFlowCello 300-CycleMicroFlowCello 300-CycleStandardFlowCello 500-CycleNanoFlowCello 500-CycleStandardFlowCell
§ MiliQH2O§ Sodiumhydroxide
Equipment/Supplies§ Singlechannelmicropipettes§ Kimwipes§ Lenspaper§ IlluminaMiSeq§ 1.5mLlow-bindmicrocentrifugetubes§ Microcentrifuge
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Step8–AnalysisofHLASequencingDataAfter sequencing theprovidedsamples, the IlluminaMiSeqautomatically createsa fastq file.When configured correctly by your bioinformaticians or IT admin, HLA Twin (the softwareincluded with Holotype HLA) automatically begins running the genotyping analysis with twoorthogonal algorithms. Please refer to the HLA Twinmanual for assistance with the correctinstallation of HLA Twin and for information on interpreting the genotyping analysis of yoursequencingdata.
Protocol sub-steps § DatatransferfromMiSeqtoanalysiscomputer§ AnalysisofdatausingHLATwin
Equipment/Supplies § 64-bitcomputerwithminimum4Coresand16GBofRAM§ Long-termstorageof2TBperMiSeqperyear
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OnsiteandRemoteTrainingOmixonprovidesavarietyoftrainingoptionstousersofHolotypeHLAandHLATwin.AlltrainingoptionsinvolveaHolotypeHLAandHLATwintrainingseminar.Theseminarsareprovidedeitheron-site or remotely using aweb conference. Laboratories have different training needs, andOmixonprovidesa5,3,or1daytrainingtomeetthoseuniquerequirements.Beforetrainingcanbeginhowever,itisimportanttofollowoursitepreparationguidetooptimizeourtimetogetherwith you. The training schedule and site preparation guide are guidelines, andwe advise allcustomerstoworkwithsupport@omixon.cominordertotailortrainingtoyourlaboratory.
SitePreparationInadditiontohavingthelabsuppliesdescribedinSteps1through8onhand,yourlabshouldalsohavethefollowingprepared:
§ Makesureyourinstruments(platefluorometer,qPCRsystem,IlluminaMiSeq,fileserver)areconnectedtoalocalnetwork.
§ Necessaryinstrumentsareavailableandingoodworkingorder.§ Thermalcyclerprogramsareinputandsavedontothedevice.§ Quantifluortemplateshavebeencreatedforyourplatefluorometer.§ PippinPrepprogramsareinputandsavedontothedevice.§ KapalibrarypreparationkittemplateshavebeencreatedforyourqPCRsystem.§ TheMiSeqhasperformed2post-runwashes.§ HLATwinhasbeensuccessfullyinstalled.
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5-day Training (highly recommended) Time Day1 Day2 Day3 Day4 Day58:00 Amplicon
quantitationSoftwaretraining
Ampliconquantitation
Softwaretraining
9:00 ExoSAPPurificationFragmentation
ExoSAPPurificationFragmentation
10:00 Pre-trainingpresentation
End-repair End-repair
11:00 Worksheetdemonstration
LigationandPooling
Questionandanswer
LigationandPooling
Questionandanswer
12:00 Lunchbreak AMPureXPconcentration
Lunchbreak AMPureXPconcentration
Lunchbreak
13:00 Equipmentandreagentcheck
PippinsizeselectionLunchbreak
PippinsizeselectionLunchbreak
Softwaretraining
14:00 gDNAdilutionandprimermixformulation
Qubit(orqPCR–optional)
gDNAdilutionandPrimerMixformulation
Qubit(orqPCR–optional)
15:00 LR-PCRamplification
LoadingMiSeq LR-PCRamplification
LoadingMiSeq
3-day Training (recommended) Time Day1 Day2 Day38:00 Ampliconquantitation Softwaretraining9:00 ExoSAPpurification
Fragmentation
10:00 Pre-trainingpresentation End-repair 11:00 Worksheetdemonstration Ligationandpooling Questionandanswer12:00 Lunchbreak AMPureXPconcentration Lunchbreak13:00 Equipmentandreagent
checkPippinSizeselectionLunchbreak
Softwaretraining
14:00 gDNAdilutionandprimermixformulation
Qubit(orqPCR-optional)
15:00 LR-PCRamplification LoadingMiSeq
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1-day Training (by special request only) Time PrepDay Day18:00 Ampliconquantitation9:00 ExoSAPPurification,Fragmentation10:00 End-repair11:00 Ligationandpooling12:00 AMPureXPconcentration13:00 Pippinsizeselection
Lunchbreak14:00 Qubit(orqPCR–optional)15:00 gDNA dilution, primer mix formulation,
andLR-PCRamplificationLoadingMiSeq
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TechnicalAssistanceForgeneralassistancewiththisprotocolcontactsupport@omixon.comSafetyDataSheetsareavailableatwww.omixon.com/holotype-hla-documentation/msds
PhoneSupport:UnitedStates|+1(617)500-0790Europe|+36705748001RestofWorld|+1(617)500-0790