Differences werefound inmacrophages bystudying_______bacteria in mice.cDNA synthesis:primed mRNA isconverted intocDNA through_______ Anadvantage ofDNAMicroarraysis _________Studyquantified_____ cellsas low risk2.4% ACEpositivitywas found in________cells Onetechnique forcell isolationis _______Studyquantified_____ cellsas high riskOnetechnique forcell isolationis _______Surprisingly,______ cellshad lowACE2expressionqPCR is____ thanRNA seq.Libraryamplification ismost commonlydone with ____Oneconsideration ofchoosing anRNA seqplatformis_____RNAfragmentationhas __ majorapproachesThe 5thstep ofscRNA seqis ______Anadvantage ofscRNA seqis _____Onelimitation ofdual RNA-seq is _____TheNorthern blotwas inventedin _____Select organfailure fromCOVID-19could be due to_____expression______primers areused for celllysis in RNAseq.If RNA is low,______ mightbe difficult ina Northernblot.RNA seq isa type of_____sequencingIn RNA seqbeforefragmentation,RNA must be________DNAMicroarraysand Northernblots cannotquantify ____genes.Adaptorligationprepares each____ strand toligate.Differences werefound inmacrophages bystudying_______bacteria in mice.cDNA synthesis:primed mRNA isconverted intocDNA through_______ Anadvantage ofDNAMicroarraysis _________Studyquantified_____ cellsas low risk2.4% ACEpositivitywas found in________cells Onetechnique forcell isolationis _______Studyquantified_____ cellsas high riskOnetechnique forcell isolationis _______Surprisingly,______ cellshad lowACE2expressionqPCR is____ thanRNA seq.Libraryamplification ismost commonlydone with ____Oneconsideration ofchoosing anRNA seqplatformis_____RNAfragmentationhas __ majorapproachesThe 5thstep ofscRNA seqis ______Anadvantage ofscRNA seqis _____Onelimitation ofdual RNA-seq is _____TheNorthern blotwas inventedin _____Select organfailure fromCOVID-19could be due to_____expression______primers areused for celllysis in RNAseq.If RNA is low,______ mightbe difficult ina Northernblot.RNA seq isa type of_____sequencingIn RNA seqbeforefragmentation,RNA must be________DNAMicroarraysand Northernblots cannotquantify ____genes.Adaptorligationprepares each____ strand toligate.

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