Surprisingly,______ cellshad lowACE2expressionOnetechnique forcell isolationis _______Adaptorligationprepares each____ strand toligate.Onelimitation ofdual RNA-seq is _____Oneconsideration ofchoosing anRNA seqplatformis_____RNAfragmentationhas __ majorapproachesqPCR is____ thanRNA seq.Select organfailure fromCOVID-19could be due to_____expressionRNA seq isa type of_____sequencingThe 5thstep ofscRNA seqis ______DNAMicroarraysand Northernblots cannotquantify ____genes.______primers areused for celllysis in RNAseq.In RNA seqbeforefragmentation,RNA must be________Onetechnique forcell isolationis _______Studyquantified_____ cellsas low riskStudyquantified_____ cellsas high risk2.4% ACEpositivitywas found in________cells Anadvantage ofscRNA seqis _____If RNA is low,______ mightbe difficult ina Northernblot.cDNA synthesis:primed mRNA isconverted intocDNA through_______ TheNorthern blotwas inventedin _____Libraryamplification ismost commonlydone with ____Differences werefound inmacrophages bystudying_______bacteria in mice.Anadvantage ofDNAMicroarraysis _________Surprisingly,______ cellshad lowACE2expressionOnetechnique forcell isolationis _______Adaptorligationprepares each____ strand toligate.Onelimitation ofdual RNA-seq is _____Oneconsideration ofchoosing anRNA seqplatformis_____RNAfragmentationhas __ majorapproachesqPCR is____ thanRNA seq.Select organfailure fromCOVID-19could be due to_____expressionRNA seq isa type of_____sequencingThe 5thstep ofscRNA seqis ______DNAMicroarraysand Northernblots cannotquantify ____genes.______primers areused for celllysis in RNAseq.In RNA seqbeforefragmentation,RNA must be________Onetechnique forcell isolationis _______Studyquantified_____ cellsas low riskStudyquantified_____ cellsas high risk2.4% ACEpositivitywas found in________cells Anadvantage ofscRNA seqis _____If RNA is low,______ mightbe difficult ina Northernblot.cDNA synthesis:primed mRNA isconverted intocDNA through_______ TheNorthern blotwas inventedin _____Libraryamplification ismost commonlydone with ____Differences werefound inmacrophages bystudying_______bacteria in mice.Anadvantage ofDNAMicroarraysis _________

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