ThymineWhich of thenucleotidesbelow isfound in DNAbut not RNA?YWhatshape isthe MITadapter?Removessalt/MM/carrierover andprecipitatesDNAWhat is thepurpose ofethanol in abeadpurification?Index andidentifyindividualsamplesWhat isthepurpose ofthe RBC?4How manycolors doesHiSeq have?qPCRTechnologyused formeasuringDNA usingPCR.Fungi andbacteria canhave toughcell wallsWhy is enzymetreatment sometimesrequired to purifyfungal or bacterialDNA, but not DNAfrom tissue culturecells?FrederickSangerWho is theinventor offirstgenerationsequencing?ProcaryoticcellsWhich type ofcell is older:Procaryoticoreucaryotic?P5/P7How doesthe librarybind to theflow cell?T4PNKWhat enzymeadds a5’phosphate?BindsDNAWhat is thepurpose ofbeads in abeadpurification?LacksexonucleaseactivityHow does theKlenowfragment in A-tailing differfrom EndRepair?Removes inhibitorylibrary and primerdimers in samples toimprove clusteringefficiency onNovaSeqWhat is thepurpose ofPippinEnrichment?KaryMullisWho istheinventorof PCR?Thereis noneWhat’s thepassingCD onNovaSeq?DNA iseluted inaqueoussolutionWhat is thepurpose ofDSB in beadpurification?48How manyampliconsare in theSNP tracerpool?Translationribosomal rna isa component ofribosomes,which are thesites ofDigest_DNAThe primaryfunction ofDNAse I is toNucleicacids andproteinsWhat types ofmolecules doesmolecularbiology primarilydeal with?Denaturesdouble strandedDNA (wesequence singlestranded DNA)What is thepurpose ofNaOH forsequencingprep?TransmissiongeneticsWhat wasthe earlywork ongenesreferred to?UAA__UAG__UGAWhat arethe threeterminationcodons?mRNAIf a poly-T or poly-Uresin is incubatedwith purified totalRNA, what type ofRNA will make up themajority of materialthat hybridizes to thebeads?ByelectrophoresisHow doesthe Pippinpurify?Inhibitsreaction,chelatesMg2+How doesEDTAfunction afterLigation?5 to3What is thedirectionalityof DNA?Denaturation,Annealing,ExtensionWhat arethe 3steps ofPCR?Better_sensitivityWhat is theprimaryadvantage ofsilver stain overother stainingmethods?1%How muchof DNAcodes forproteins?Fluorescentlybinds doublestrandedDNAHow doesquant-itwork?Better_sensitivityWhat is theprimaryadvantage ofsilver stain overother stainingmethods?5ulWhat is thevolume ofEDTA addedat Ligation?5%_GelIf you are attempting toresolve DNA fragmentsthat range from 100 bpto 500 bp, whatconcentration ofagarose gel wouldprovide the bestfragment separation?35ulHow manyuL’s ofDSB/TW aredispensedinto -LELU?DenaturingagentsBuffer Additivessuch asFormamide andUrea serve whatpurpose?tRNAWhich type ofRNA bindsindividual aminoacids andrecognizes thematching codons?Ribosomal___ RNA formspart of the cellstructure thatprovides the sitewhere proteins aresynthesizedFree!Health,flammability,reactivity,other/corrosiveWhat do eachof the MSDScolors mean -blue, red,yellow, andwhite?ProteinWhat doesWesternblottarget?NucleosomeDNAwrappedaround ahistone coreSecondaryAn ɑ-helix isan exampleof _______proteinstructure.WithinanucleusWhere is theDNA in aneucaryoticcells?RNAWhat doesNorthernblottarget?Ultraviolet_lightPyrimidinedimers arecaused by:2How manycolors doesNovaSeqhave?small_and_negativity_chargedIn a capillaryelectrophoresissystem, which ofthese particles willmigrate mostrapidly through thecapillary?5’P and3’AWhatcomponentsare neededfor ligation tooccur?Intercalates,and minorgroovebinderHow doespicogreenbindDNA?DNAWhat doesSouthernblottarget?SpecificTargetAmplificationReactionWhatdoesSTARstand for?25ulHow muchdsb/TW isdispensedinto the -SLIB2?45ulHow many uL’sof DSB/TW aredispensed intothe Long/Shortplates?Free!Alanine_Valine_LeucineWhich aminoacids have apyruvatesyntheticprecursor?phenylalanine,tyrosine,tryptophanWhichaminoacids arearomatic?3 to5What is thedirectionality ofthecomplementarystrand?AntiparallelWhat istheorientationof DNA?80%Whatpercentage ofethanol do weuse for washplates duringKF steps?MTM/mLWhat is thequantitativemeasurementof Signatera?PlasmainbloodWhere iscfDNAisolatedfrom?NextGenerationSequencingA technology used todetermine thesequence of DNA orRNA to study geneticvariation associatedwith diseases orother biologicalphenomena 116How manyampliconsare in thebespokeprimer pool?Bacteriophage(balanced basepattern), forsequencing QCWhat isPhiX?Digest_DNAThe primaryfunction ofDNAse I is to3How manyhydrogenbonds arein G-C?Conjugated_sugarsA glycoproteinis a protein thatis _________with__________.  Size_in_bpWhat factordetermines theconcentration ofagarose gelused for bandseparation?What isMolecularbiology?Hybrid discipline thatcombines elementsof genetics andbiochemistry. It is thestudy of genestructure and functionat the molecularlevel.Post LibAmp,SLIB2What workflowstep/platecontains bubbleproducts?TaqpolymeraseWhatenzymeputs a3’A?RegulatingGeneexpressionWhat isthefunction ofmiRNA?ThymineWhich of thenucleotidesbelow isfound in DNAbut not RNA?YWhatshape isthe MITadapter?Removessalt/MM/carrierover andprecipitatesDNAWhat is thepurpose ofethanol in abeadpurification?Index andidentifyindividualsamplesWhat isthepurpose ofthe RBC?4How manycolors doesHiSeq have?qPCRTechnologyused formeasuringDNA usingPCR.Fungi andbacteria canhave toughcell wallsWhy is enzymetreatment sometimesrequired to purifyfungal or bacterialDNA, but not DNAfrom tissue culturecells?FrederickSangerWho is theinventor offirstgenerationsequencing?ProcaryoticcellsWhich type ofcell is older:Procaryoticoreucaryotic?P5/P7How doesthe librarybind to theflow cell?T4PNKWhat enzymeadds a5’phosphate?BindsDNAWhat is thepurpose ofbeads in abeadpurification?LacksexonucleaseactivityHow does theKlenowfragment in A-tailing differfrom EndRepair?Removes inhibitorylibrary and primerdimers in samples toimprove clusteringefficiency onNovaSeqWhat is thepurpose ofPippinEnrichment?KaryMullisWho istheinventorof PCR?Thereis noneWhat’s thepassingCD onNovaSeq?DNA iseluted inaqueoussolutionWhat is thepurpose ofDSB in beadpurification?48How manyampliconsare in theSNP tracerpool?Translationribosomal rna isa component ofribosomes,which are thesites ofDigest_DNAThe primaryfunction ofDNAse I is toNucleicacids andproteinsWhat types ofmolecules doesmolecularbiology primarilydeal with?Denaturesdouble strandedDNA (wesequence singlestranded DNA)What is thepurpose ofNaOH forsequencingprep?TransmissiongeneticsWhat wasthe earlywork ongenesreferred to?UAA__UAG__UGAWhat arethe threeterminationcodons?mRNAIf a poly-T or poly-Uresin is incubatedwith purified totalRNA, what type ofRNA will make up themajority of materialthat hybridizes to thebeads?ByelectrophoresisHow doesthe Pippinpurify?Inhibitsreaction,chelatesMg2+How doesEDTAfunction afterLigation?5 to3What is thedirectionalityof DNA?Denaturation,Annealing,ExtensionWhat arethe 3steps ofPCR?Better_sensitivityWhat is theprimaryadvantage ofsilver stain overother stainingmethods?1%How muchof DNAcodes forproteins?Fluorescentlybinds doublestrandedDNAHow doesquant-itwork?Better_sensitivityWhat is theprimaryadvantage ofsilver stain overother stainingmethods?5ulWhat is thevolume ofEDTA addedat Ligation?5%_GelIf you are attempting toresolve DNA fragmentsthat range from 100 bpto 500 bp, whatconcentration ofagarose gel wouldprovide the bestfragment separation?35ulHow manyuL’s ofDSB/TW aredispensedinto -LELU?DenaturingagentsBuffer Additivessuch asFormamide andUrea serve whatpurpose?tRNAWhich type ofRNA bindsindividual aminoacids andrecognizes thematching codons?Ribosomal___ RNA formspart of the cellstructure thatprovides the sitewhere proteins aresynthesizedFree!Health,flammability,reactivity,other/corrosiveWhat do eachof the MSDScolors mean -blue, red,yellow, andwhite?ProteinWhat doesWesternblottarget?NucleosomeDNAwrappedaround ahistone coreSecondaryAn ɑ-helix isan exampleof _______proteinstructure.WithinanucleusWhere is theDNA in aneucaryoticcells?RNAWhat doesNorthernblottarget?Ultraviolet_lightPyrimidinedimers arecaused by:2How manycolors doesNovaSeqhave?small_and_negativity_chargedIn a capillaryelectrophoresissystem, which ofthese particles willmigrate mostrapidly through thecapillary?5’P and3’AWhatcomponentsare neededfor ligation tooccur?Intercalates,and minorgroovebinderHow doespicogreenbindDNA?DNAWhat doesSouthernblottarget?SpecificTargetAmplificationReactionWhatdoesSTARstand for?25ulHow muchdsb/TW isdispensedinto the -SLIB2?45ulHow many uL’sof DSB/TW aredispensed intothe Long/Shortplates?Free!Alanine_Valine_LeucineWhich aminoacids have apyruvatesyntheticprecursor?phenylalanine,tyrosine,tryptophanWhichaminoacids arearomatic?3 to5What is thedirectionality ofthecomplementarystrand?AntiparallelWhat istheorientationof DNA?80%Whatpercentage ofethanol do weuse for washplates duringKF steps?MTM/mLWhat is thequantitativemeasurementof Signatera?PlasmainbloodWhere iscfDNAisolatedfrom?NextGenerationSequencingA technology used todetermine thesequence of DNA orRNA to study geneticvariation associatedwith diseases orother biologicalphenomena 116How manyampliconsare in thebespokeprimer pool?Bacteriophage(balanced basepattern), forsequencing QCWhat isPhiX?Digest_DNAThe primaryfunction ofDNAse I is to3How manyhydrogenbonds arein G-C?Conjugated_sugarsA glycoproteinis a protein thatis _________with__________.  Size_in_bpWhat factordetermines theconcentration ofagarose gelused for bandseparation?What isMolecularbiology?Hybrid discipline thatcombines elementsof genetics andbiochemistry. It is thestudy of genestructure and functionat the molecularlevel.Post LibAmp,SLIB2What workflowstep/platecontains bubbleproducts?TaqpolymeraseWhatenzymeputs a3’A?RegulatingGeneexpressionWhat isthefunction ofmiRNA?

Signatera Molecular Biology - Call List

(Print) Use this randomly generated list as your call list when playing the game. Place some kind of mark (like an X, a checkmark, a dot, tally mark, etc) on each cell as you announce it, to keep track. You can also cut out each item, place them in a bag and pull words from the bag.


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  1. T-Which of the nucleotides below is found in DNA but not RNA?
    T-Thymine
  2. R-What shape is the MIT adapter?
    R-Y
  3. M-What is the purpose of ethanol in a bead purification?
    M-Removes salt/MM/carrier over and precipitates DNA
  4. A-What is the purpose of the RBC?
    A-Index and identify individual samples
  5. S-How many colors does HiSeq have?
    S-4
  6. M-Technology used for measuring DNA using PCR.
    M-qPCR
  7. A-Why is enzyme treatment sometimes required to purify fungal or bacterial DNA, but not DNA from tissue culture cells?
    A-Fungi and bacteria can have tough cell walls
  8. T-Who is the inventor of first generation sequencing?
    T-Frederick Sanger
  9. A-Which type of cell is older: Procaryotic or eucaryotic?
    A-Procaryotic cells
  10. T-How does the library bind to the flow cell?
    T-P5/P7
  11. M-What enzyme adds a 5’phosphate?
    M-T4 PNK
  12. M-What is the purpose of beads in a bead purification?
    M-Binds DNA
  13. T-How does the Klenow fragment in A-tailing differ from End Repair?
    T-Lacks exonuclease activity
  14. T-What is the purpose of Pippin Enrichment?
    T-Removes inhibitory library and primer dimers in samples to improve clustering efficiency on NovaSeq
  15. T-Who is the inventor of PCR?
    T-Kary Mullis
  16. A-What’s the passing CD on NovaSeq?
    A-There is none
  17. A-What is the purpose of DSB in bead purification?
    A-DNA is eluted in aqueous solution
  18. S-How many amplicons are in the SNP tracer pool?
    S-48
  19. R-ribosomal rna is a component of ribosomes, which are the sites of
    R-Translation
  20. T-The primary function of DNAse I is to
    T-Digest_DNA
  21. T-What types of molecules does molecular biology primarily deal with?
    T-Nucleic acids and proteins
  22. T-What is the purpose of NaOH for sequencing prep?
    T-Denatures double stranded DNA (we sequence single stranded DNA)
  23. R-What was the early work on genes referred to?
    R-Transmission genetics
  24. M-What are the three termination codons?
    M-UAA__UAG__UGA
  25. R-If a poly-T or poly-U resin is incubated with purified total RNA, what type of RNA will make up the majority of material that hybridizes to the beads?
    R-mRNA
  26. A-How does the Pippin purify?
    A-By electrophoresis
  27. T-How does EDTA function after Ligation?
    T-Inhibits reaction, chelates Mg2+
  28. S-What is the directionality of DNA?
    S-5 to 3
  29. M-What are the 3 steps of PCR?
    M-Denaturation, Annealing, Extension
  30. M-What is the primary advantage of silver stain over other staining methods?
    M-Better_sensitivity
  31. S-How much of DNA codes for proteins?
    S-1%
  32. T-How does quant-it work?
    T-Fluorescently binds double stranded DNA
  33. R-What is the primary advantage of silver stain over other staining methods?
    R-Better_sensitivity
  34. S-What is the volume of EDTA added at Ligation?
    S-5ul
  35. S-If you are attempting to resolve DNA fragments that range from 100 bp to 500 bp, what concentration of agarose gel would provide the best fragment separation?
    S-5%_Gel
  36. S-How many uL’s of DSB/TW are dispensed into -LELU?
    S-35ul
  37. R-Buffer Additives such as Formamide and Urea serve what purpose?
    R-Denaturing agents
  38. R-Which type of RNA binds individual amino acids and recognizes the matching codons?
    R-tRNA
  39. R-___ RNA forms part of the cell structure that provides the site where proteins are synthesized
    R-Ribosomal
  40. A-Free!
  41. M-What do each of the MSDS colors mean - blue, red, yellow, and white?
    M-Health, flammability, reactivity, other/corrosive
  42. M-What does Western blot target?
    M-Protein
  43. A-DNA wrapped around a histone core
    A-Nucleosome
  44. R-An ɑ-helix is an example of _______ protein structure.
    R-Secondary
  45. T-Where is the DNA in an eucaryotic cells?
    T-Within a nucleus
  46. A-What does Northern blot target?
    A-RNA
  47. M-Pyrimidine dimers are caused by:
    M-Ultraviolet_light
  48. S-How many colors does NovaSeq have?
    S-2
  49. A-In a capillary electrophoresis system, which of these particles will migrate most rapidly through the capillary?
    A-small_and _negativity_charged
  50. S-What components are needed for ligation to occur?
    S-5’P and 3’A
  51. T-How does picogreen bind DNA?
    T-Intercalates, and minor groove binder
  52. A-What does Southern blot target?
    A-DNA
  53. M-What does STAR stand for?
    M-Specific Target Amplification Reaction
  54. S-How much dsb/TW is dispensed into the -SLIB2?
    S-25ul
  55. S-How many uL’s of DSB/TW are dispensed into the Long/Short plates?
    S-45ul
  56. A-Free!
  57. T-Which amino acids have a pyruvate synthetic precursor?
    T-Alanine_ Valine_Leucine
  58. T-Which amino acids are aromatic?
    T-phenylalanine, tyrosine, tryptophan
  59. S-What is the directionality of the complementary strand?
    S-3 to 5
  60. M-What is the orientation of DNA?
    M-Antiparallel
  61. S-What percentage of ethanol do we use for wash plates during KF steps?
    S-80%
  62. R-What is the quantitative measurement of Signatera?
    R-MTM/mL
  63. R-Where is cfDNA isolated from?
    R-Plasma in blood
  64. A-A technology used to determine the sequence of DNA or RNA to study genetic variation associated with diseases or other biological phenomena 1
    A-Next Generation Sequencing
  65. S-How many amplicons are in the bespoke primer pool?
    S-16
  66. R-What is PhiX?
    R-Bacteriophage (balanced base pattern), for sequencing QC
  67. A-The primary function of DNAse I is to
    A-Digest_DNA
  68. S-How many hydrogen bonds are in G-C?
    S-3
  69. R-A glycoprotein is a protein that is _________ with __________.
    R-Conjugated_sugars
  70. M-What factor determines the concentration of agarose gel used for band separation?
    M- Size_in_bp
  71. M-Hybrid discipline that combines elements of genetics and biochemistry. It is the study of gene structure and function at the molecular level.
    M-What is Molecular biology?
  72. R-What workflow step/plate contains bubble products?
    R-Post Lib Amp, SLIB2
  73. M-What enzyme puts a 3’A?
    M-Taq polymerase
  74. R-What is the function of miRNA?
    R-Regulating Gene expression