Differences werefound inmacrophages bystudying_______bacteria in mice.Select organfailure fromCOVID-19could be due to_____expression______primers areused for celllysis in RNAseq.Studyquantified_____ cellsas low riskAnadvantage ofscRNA seqis _____RNAfragmentationhas __ majorapproachesOnetechnique forcell isolationis _______Onetechnique forcell isolationis _______DNAMicroarraysand Northernblots cannotquantify ____genes.qPCR is____ thanRNA seq.If RNA is low,______ mightbe difficult ina Northernblot.Adaptorligationprepares each____ strand toligate.Anadvantage ofDNAMicroarraysis _________Onelimitation ofdual RNA-seq is _____Studyquantified_____ cellsas high risk2.4% ACEpositivitywas found in________cells cDNA synthesis:primed mRNA isconverted intocDNA through_______ RNA seq isa type of_____sequencingIn RNA seqbeforefragmentation,RNA must be________Libraryamplification ismost commonlydone with ____TheNorthern blotwas inventedin _____Surprisingly,______ cellshad lowACE2expressionOneconsideration ofchoosing anRNA seqplatformis_____The 5thstep ofscRNA seqis ______Differences werefound inmacrophages bystudying_______bacteria in mice.Select organfailure fromCOVID-19could be due to_____expression______primers areused for celllysis in RNAseq.Studyquantified_____ cellsas low riskAnadvantage ofscRNA seqis _____RNAfragmentationhas __ majorapproachesOnetechnique forcell isolationis _______Onetechnique forcell isolationis _______DNAMicroarraysand Northernblots cannotquantify ____genes.qPCR is____ thanRNA seq.If RNA is low,______ mightbe difficult ina Northernblot.Adaptorligationprepares each____ strand toligate.Anadvantage ofDNAMicroarraysis _________Onelimitation ofdual RNA-seq is _____Studyquantified_____ cellsas high risk2.4% ACEpositivitywas found in________cells cDNA synthesis:primed mRNA isconverted intocDNA through_______ RNA seq isa type of_____sequencingIn RNA seqbeforefragmentation,RNA must be________Libraryamplification ismost commonlydone with ____TheNorthern blotwas inventedin _____Surprisingly,______ cellshad lowACE2expressionOneconsideration ofchoosing anRNA seqplatformis_____The 5thstep ofscRNA seqis ______

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