qPCR is____ thanRNA seq.2.4% ACEpositivitywas found in________cells Studyquantified_____ cellsas low riskSurprisingly,______ cellshad lowACE2expressionRNAfragmentationhas __ majorapproachescDNA synthesis:primed mRNA isconverted intocDNA through_______ Select organfailure fromCOVID-19could be due to_____expressionThe 5thstep ofscRNA seqis ______DNAMicroarraysand Northernblots cannotquantify ____genes.Anadvantage ofscRNA seqis ___________primers areused for celllysis in RNAseq.Adaptorligationprepares each____ strand toligate.Anadvantage ofDNAMicroarraysis _________Onetechnique forcell isolationis _______Onetechnique forcell isolationis _______Onelimitation ofdual RNA-seq is _____RNA seq isa type of_____sequencingDifferences werefound inmacrophages bystudying_______bacteria in mice.TheNorthern blotwas inventedin _____If RNA is low,______ mightbe difficult ina Northernblot.Studyquantified_____ cellsas high riskOneconsideration ofchoosing anRNA seqplatformis_____In RNA seqbeforefragmentation,RNA must be________Libraryamplification ismost commonlydone with ____qPCR is____ thanRNA seq.2.4% ACEpositivitywas found in________cells Studyquantified_____ cellsas low riskSurprisingly,______ cellshad lowACE2expressionRNAfragmentationhas __ majorapproachescDNA synthesis:primed mRNA isconverted intocDNA through_______ Select organfailure fromCOVID-19could be due to_____expressionThe 5thstep ofscRNA seqis ______DNAMicroarraysand Northernblots cannotquantify ____genes.Anadvantage ofscRNA seqis ___________primers areused for celllysis in RNAseq.Adaptorligationprepares each____ strand toligate.Anadvantage ofDNAMicroarraysis _________Onetechnique forcell isolationis _______Onetechnique forcell isolationis _______Onelimitation ofdual RNA-seq is _____RNA seq isa type of_____sequencingDifferences werefound inmacrophages bystudying_______bacteria in mice.TheNorthern blotwas inventedin _____If RNA is low,______ mightbe difficult ina Northernblot.Studyquantified_____ cellsas high riskOneconsideration ofchoosing anRNA seqplatformis_____In RNA seqbeforefragmentation,RNA must be________Libraryamplification ismost commonlydone with ____

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