The 5thstep ofscRNA seqis ______qPCR is____ thanRNA seq.Onetechnique forcell isolationis _______2.4% ACEpositivitywas found in________cells DNAMicroarraysand Northernblots cannotquantify ____genes.RNAfragmentationhas __ majorapproachesStudyquantified_____ cellsas low riskAdaptorligationprepares each____ strand toligate.If RNA is low,______ mightbe difficult ina Northernblot.Anadvantage ofscRNA seqis _____Onelimitation ofdual RNA-seq is _____cDNA synthesis:primed mRNA isconverted intocDNA through_______ Select organfailure fromCOVID-19could be due to_____expressionAnadvantage ofDNAMicroarraysis _________In RNA seqbeforefragmentation,RNA must be________Onetechnique forcell isolationis _____________primers areused for celllysis in RNAseq.Surprisingly,______ cellshad lowACE2expressionTheNorthern blotwas inventedin _____Studyquantified_____ cellsas high riskRNA seq isa type of_____sequencingOneconsideration ofchoosing anRNA seqplatformis_____Libraryamplification ismost commonlydone with ____Differences werefound inmacrophages bystudying_______bacteria in mice.The 5thstep ofscRNA seqis ______qPCR is____ thanRNA seq.Onetechnique forcell isolationis _______2.4% ACEpositivitywas found in________cells DNAMicroarraysand Northernblots cannotquantify ____genes.RNAfragmentationhas __ majorapproachesStudyquantified_____ cellsas low riskAdaptorligationprepares each____ strand toligate.If RNA is low,______ mightbe difficult ina Northernblot.Anadvantage ofscRNA seqis _____Onelimitation ofdual RNA-seq is _____cDNA synthesis:primed mRNA isconverted intocDNA through_______ Select organfailure fromCOVID-19could be due to_____expressionAnadvantage ofDNAMicroarraysis _________In RNA seqbeforefragmentation,RNA must be________Onetechnique forcell isolationis _____________primers areused for celllysis in RNAseq.Surprisingly,______ cellshad lowACE2expressionTheNorthern blotwas inventedin _____Studyquantified_____ cellsas high riskRNA seq isa type of_____sequencingOneconsideration ofchoosing anRNA seqplatformis_____Libraryamplification ismost commonlydone with ____Differences werefound inmacrophages bystudying_______bacteria in mice.

RNA Seq Bingo - Call List

(Print) Use this randomly generated list as your call list when playing the game. There is no need to say the BINGO column name. 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. The 5th step of scRNA seq is ______
  2. qPCR is ____ than RNA seq.
  3. One technique for cell isolation is _______
  4. 2.4% ACE positivity was found in ________ cells
  5. DNA Microarrays and Northern blots cannot quantify ____ genes.
  6. RNA fragmentation has __ major approaches
  7. Study quantified _____ cells as low risk
  8. Adaptor ligation prepares each ____ strand to ligate.
  9. If RNA is low, ______ might be difficult in a Northern blot.
  10. An advantage of scRNA seq is _____
  11. One limitation of dual RNA-seq is _____
  12. cDNA synthesis: primed mRNA is converted into cDNA through _______
  13. Select organ failure from COVID-19 could be due to _____ expression
  14. An advantage of DNA Microarrays is _________
  15. In RNA seq before fragmentation, RNA must be ________
  16. One technique for cell isolation is _______
  17. ______ primers are used for cell lysis in RNA seq.
  18. Surprisingly, ______ cells had low ACE2 expression
  19. The Northern blot was invented in _____
  20. Study quantified _____ cells as high risk
  21. RNA seq is a type of _____ sequencing
  22. One consideration of choosing an RNA seq platform is_____
  23. Library amplification is most commonly done with ____
  24. Differences were found in macrophages by studying _______ bacteria in mice.