RNA seq isa type of_____sequencingOneconsideration ofchoosing anRNA seqplatformis_____DNAMicroarraysand Northernblots cannotquantify ____genes.______primers areused for celllysis in RNAseq.qPCR is____ thanRNA seq.Anadvantage ofDNAMicroarraysis _________RNAfragmentationhas __ majorapproachesLibraryamplification ismost commonlydone with ____Differences werefound inmacrophages bystudying_______bacteria in mice.Select organfailure fromCOVID-19could be due to_____expressionTheNorthern blotwas inventedin _____If RNA is low,______ mightbe difficult ina Northernblot.Studyquantified_____ cellsas high riskAdaptorligationprepares each____ strand toligate.Surprisingly,______ cellshad lowACE2expressionOnetechnique forcell isolationis _______In RNA seqbeforefragmentation,RNA must be________The 5thstep ofscRNA seqis ______Onelimitation ofdual RNA-seq is _____2.4% ACEpositivitywas found in________cells Anadvantage ofscRNA seqis _____cDNA synthesis:primed mRNA isconverted intocDNA through_______ Onetechnique forcell isolationis _______Studyquantified_____ cellsas low riskRNA seq isa type of_____sequencingOneconsideration ofchoosing anRNA seqplatformis_____DNAMicroarraysand Northernblots cannotquantify ____genes.______primers areused for celllysis in RNAseq.qPCR is____ thanRNA seq.Anadvantage ofDNAMicroarraysis _________RNAfragmentationhas __ majorapproachesLibraryamplification ismost commonlydone with ____Differences werefound inmacrophages bystudying_______bacteria in mice.Select organfailure fromCOVID-19could be due to_____expressionTheNorthern blotwas inventedin _____If RNA is low,______ mightbe difficult ina Northernblot.Studyquantified_____ cellsas high riskAdaptorligationprepares each____ strand toligate.Surprisingly,______ cellshad lowACE2expressionOnetechnique forcell isolationis _______In RNA seqbeforefragmentation,RNA must be________The 5thstep ofscRNA seqis ______Onelimitation ofdual RNA-seq is _____2.4% ACEpositivitywas found in________cells Anadvantage ofscRNA seqis _____cDNA synthesis:primed mRNA isconverted intocDNA through_______ Onetechnique forcell isolationis _______Studyquantified_____ cellsas low risk

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