Onetechnique forcell isolationis _______RNA seq isa type of_____sequencingThe 5thstep ofscRNA seqis ______Libraryamplification ismost commonlydone with ____Oneconsideration ofchoosing anRNA seqplatformis___________primers areused for celllysis in RNAseq.Onelimitation ofdual RNA-seq is _____Select organfailure fromCOVID-19could be due to_____expression2.4% ACEpositivitywas found in________cells In RNA seqbeforefragmentation,RNA must be________Anadvantage ofscRNA seqis _____Anadvantage ofDNAMicroarraysis _________Differences werefound inmacrophages bystudying_______bacteria in mice.RNAfragmentationhas __ majorapproachesqPCR is____ thanRNA seq.Studyquantified_____ cellsas low riskTheNorthern blotwas inventedin _____Onetechnique forcell isolationis _______If RNA is low,______ mightbe difficult ina Northernblot.Surprisingly,______ cellshad lowACE2expressioncDNA synthesis:primed mRNA isconverted intocDNA through_______ Studyquantified_____ cellsas high riskAdaptorligationprepares each____ strand toligate.DNAMicroarraysand Northernblots cannotquantify ____genes.Onetechnique forcell isolationis _______RNA seq isa type of_____sequencingThe 5thstep ofscRNA seqis ______Libraryamplification ismost commonlydone with ____Oneconsideration ofchoosing anRNA seqplatformis___________primers areused for celllysis in RNAseq.Onelimitation ofdual RNA-seq is _____Select organfailure fromCOVID-19could be due to_____expression2.4% ACEpositivitywas found in________cells In RNA seqbeforefragmentation,RNA must be________Anadvantage ofscRNA seqis _____Anadvantage ofDNAMicroarraysis _________Differences werefound inmacrophages bystudying_______bacteria in mice.RNAfragmentationhas __ majorapproachesqPCR is____ thanRNA seq.Studyquantified_____ cellsas low riskTheNorthern blotwas inventedin _____Onetechnique forcell isolationis _______If RNA is low,______ mightbe difficult ina Northernblot.Surprisingly,______ cellshad lowACE2expressioncDNA synthesis:primed mRNA isconverted intocDNA through_______ Studyquantified_____ cellsas high riskAdaptorligationprepares each____ strand toligate.DNAMicroarraysand Northernblots cannotquantify ____genes.

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