RNA seq isa type of_____sequencingSurprisingly,______ cellshad lowACE2expressionLibraryamplification ismost commonlydone with ____Differences werefound inmacrophages bystudying_______bacteria in mice.______primers areused for celllysis in RNAseq.2.4% ACEpositivitywas found in________cells Oneconsideration ofchoosing anRNA seqplatformis_____cDNA synthesis:primed mRNA isconverted intocDNA through_______ Onelimitation ofdual RNA-seq is _____RNAfragmentationhas __ majorapproachesOnetechnique forcell isolationis _______Studyquantified_____ cellsas high riskIf RNA is low,______ mightbe difficult ina Northernblot.TheNorthern blotwas inventedin _____Studyquantified_____ cellsas low riskAnadvantage ofDNAMicroarraysis _________DNAMicroarraysand Northernblots cannotquantify ____genes.In RNA seqbeforefragmentation,RNA must be________Anadvantage ofscRNA seqis _____Onetechnique forcell isolationis _______Select organfailure fromCOVID-19could be due to_____expressionThe 5thstep ofscRNA seqis ______Adaptorligationprepares each____ strand toligate.qPCR is____ thanRNA seq.RNA seq isa type of_____sequencingSurprisingly,______ cellshad lowACE2expressionLibraryamplification ismost commonlydone with ____Differences werefound inmacrophages bystudying_______bacteria in mice.______primers areused for celllysis in RNAseq.2.4% ACEpositivitywas found in________cells Oneconsideration ofchoosing anRNA seqplatformis_____cDNA synthesis:primed mRNA isconverted intocDNA through_______ Onelimitation ofdual RNA-seq is _____RNAfragmentationhas __ majorapproachesOnetechnique forcell isolationis _______Studyquantified_____ cellsas high riskIf RNA is low,______ mightbe difficult ina Northernblot.TheNorthern blotwas inventedin _____Studyquantified_____ cellsas low riskAnadvantage ofDNAMicroarraysis _________DNAMicroarraysand Northernblots cannotquantify ____genes.In RNA seqbeforefragmentation,RNA must be________Anadvantage ofscRNA seqis _____Onetechnique forcell isolationis _______Select organfailure fromCOVID-19could be due to_____expressionThe 5thstep ofscRNA seqis ______Adaptorligationprepares each____ strand toligate.qPCR is____ thanRNA seq.

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. RNA seq is a type of _____ sequencing
  2. Surprisingly, ______ cells had low ACE2 expression
  3. Library amplification is most commonly done with ____
  4. Differences were found in macrophages by studying _______ bacteria in mice.
  5. ______ primers are used for cell lysis in RNA seq.
  6. 2.4% ACE positivity was found in ________ cells
  7. One consideration of choosing an RNA seq platform is_____
  8. cDNA synthesis: primed mRNA is converted into cDNA through _______
  9. One limitation of dual RNA-seq is _____
  10. RNA fragmentation has __ major approaches
  11. One technique for cell isolation is _______
  12. Study quantified _____ cells as high risk
  13. If RNA is low, ______ might be difficult in a Northern blot.
  14. The Northern blot was invented in _____
  15. Study quantified _____ cells as low risk
  16. An advantage of DNA Microarrays is _________
  17. DNA Microarrays and Northern blots cannot quantify ____ genes.
  18. In RNA seq before fragmentation, RNA must be ________
  19. An advantage of scRNA seq is _____
  20. One technique for cell isolation is _______
  21. Select organ failure from COVID-19 could be due to _____ expression
  22. The 5th step of scRNA seq is ______
  23. Adaptor ligation prepares each ____ strand to ligate.
  24. qPCR is ____ than RNA seq.