Anadvantage ofDNAMicroarraysis _________RNA seq isa type of_____sequencingAdaptorligationprepares each____ strand toligate.TheNorthern blotwas inventedin _____qPCR is____ thanRNA seq.Anadvantage ofscRNA seqis ___________primers areused for celllysis in RNAseq.Onetechnique forcell isolationis _______Differences werefound inmacrophages bystudying_______bacteria in mice.cDNA synthesis:primed mRNA isconverted intocDNA through_______ Onelimitation ofdual RNA-seq is _____The 5thstep ofscRNA seqis ______In RNA seqbeforefragmentation,RNA must be________Oneconsideration ofchoosing anRNA seqplatformis_____Libraryamplification ismost commonlydone with ____Studyquantified_____ cellsas low riskIf RNA is low,______ mightbe difficult ina Northernblot.RNAfragmentationhas __ majorapproachesSelect organfailure fromCOVID-19could be due to_____expressionOnetechnique forcell isolationis _______2.4% ACEpositivitywas found in________cells Surprisingly,______ cellshad lowACE2expressionDNAMicroarraysand Northernblots cannotquantify ____genes.Studyquantified_____ cellsas high riskAnadvantage ofDNAMicroarraysis _________RNA seq isa type of_____sequencingAdaptorligationprepares each____ strand toligate.TheNorthern blotwas inventedin _____qPCR is____ thanRNA seq.Anadvantage ofscRNA seqis ___________primers areused for celllysis in RNAseq.Onetechnique forcell isolationis _______Differences werefound inmacrophages bystudying_______bacteria in mice.cDNA synthesis:primed mRNA isconverted intocDNA through_______ Onelimitation ofdual RNA-seq is _____The 5thstep ofscRNA seqis ______In RNA seqbeforefragmentation,RNA must be________Oneconsideration ofchoosing anRNA seqplatformis_____Libraryamplification ismost commonlydone with ____Studyquantified_____ cellsas low riskIf RNA is low,______ mightbe difficult ina Northernblot.RNAfragmentationhas __ majorapproachesSelect organfailure fromCOVID-19could be due to_____expressionOnetechnique forcell isolationis _______2.4% ACEpositivitywas found in________cells Surprisingly,______ cellshad lowACE2expressionDNAMicroarraysand Northernblots cannotquantify ____genes.Studyquantified_____ cellsas high 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. An advantage of DNA Microarrays is _________
  2. RNA seq is a type of _____ sequencing
  3. Adaptor ligation prepares each ____ strand to ligate.
  4. The Northern blot was invented in _____
  5. qPCR is ____ than RNA seq.
  6. An advantage of scRNA seq is _____
  7. ______ primers are used for cell lysis in RNA seq.
  8. One technique for cell isolation is _______
  9. Differences were found in macrophages by studying _______ bacteria in mice.
  10. cDNA synthesis: primed mRNA is converted into cDNA through _______
  11. One limitation of dual RNA-seq is _____
  12. The 5th step of scRNA seq is ______
  13. In RNA seq before fragmentation, RNA must be ________
  14. One consideration of choosing an RNA seq platform is_____
  15. Library amplification is most commonly done with ____
  16. Study quantified _____ cells as low risk
  17. If RNA is low, ______ might be difficult in a Northern blot.
  18. RNA fragmentation has __ major approaches
  19. Select organ failure from COVID-19 could be due to _____ expression
  20. One technique for cell isolation is _______
  21. 2.4% ACE positivity was found in ________ cells
  22. Surprisingly, ______ cells had low ACE2 expression
  23. DNA Microarrays and Northern blots cannot quantify ____ genes.
  24. Study quantified _____ cells as high risk