The 5thstep ofscRNA seqis ____________primers areused for celllysis in RNAseq.Anadvantage ofscRNA seqis _____qPCR is____ thanRNA seq.Studyquantified_____ cellsas high risk2.4% ACEpositivitywas found in________cells RNAfragmentationhas __ majorapproachesOnetechnique forcell isolationis _______In RNA seqbeforefragmentation,RNA must be________DNAMicroarraysand Northernblots cannotquantify ____genes.Onetechnique forcell isolationis _______TheNorthern blotwas inventedin _____cDNA synthesis:primed mRNA isconverted intocDNA through_______ Onelimitation ofdual RNA-seq is _____Oneconsideration ofchoosing anRNA seqplatformis_____RNA seq isa type of_____sequencingIf RNA is low,______ mightbe difficult ina Northernblot.Libraryamplification ismost commonlydone with ____Differences werefound inmacrophages bystudying_______bacteria in mice.Select organfailure fromCOVID-19could be due to_____expressionStudyquantified_____ cellsas low riskAnadvantage ofDNAMicroarraysis _________Adaptorligationprepares each____ strand toligate.Surprisingly,______ cellshad lowACE2expressionThe 5thstep ofscRNA seqis ____________primers areused for celllysis in RNAseq.Anadvantage ofscRNA seqis _____qPCR is____ thanRNA seq.Studyquantified_____ cellsas high risk2.4% ACEpositivitywas found in________cells RNAfragmentationhas __ majorapproachesOnetechnique forcell isolationis _______In RNA seqbeforefragmentation,RNA must be________DNAMicroarraysand Northernblots cannotquantify ____genes.Onetechnique forcell isolationis _______TheNorthern blotwas inventedin _____cDNA synthesis:primed mRNA isconverted intocDNA through_______ Onelimitation ofdual RNA-seq is _____Oneconsideration ofchoosing anRNA seqplatformis_____RNA seq isa type of_____sequencingIf RNA is low,______ mightbe difficult ina Northernblot.Libraryamplification ismost commonlydone with ____Differences werefound inmacrophages bystudying_______bacteria in mice.Select organfailure fromCOVID-19could be due to_____expressionStudyquantified_____ cellsas low riskAnadvantage ofDNAMicroarraysis _________Adaptorligationprepares each____ strand toligate.Surprisingly,______ cellshad lowACE2expression

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.


1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
  1. The 5th step of scRNA seq is ______
  2. ______ primers are used for cell lysis in RNA seq.
  3. An advantage of scRNA seq is _____
  4. qPCR is ____ than RNA seq.
  5. Study quantified _____ cells as high risk
  6. 2.4% ACE positivity was found in ________ cells
  7. RNA fragmentation has __ major approaches
  8. One technique for cell isolation is _______
  9. In RNA seq before fragmentation, RNA must be ________
  10. DNA Microarrays and Northern blots cannot quantify ____ genes.
  11. One technique for cell isolation is _______
  12. The Northern blot was invented in _____
  13. cDNA synthesis: primed mRNA is converted into cDNA through _______
  14. One limitation of dual RNA-seq is _____
  15. One consideration of choosing an RNA seq platform is_____
  16. RNA seq is a type of _____ sequencing
  17. If RNA is low, ______ might be difficult in a Northern blot.
  18. Library amplification is most commonly done with ____
  19. Differences were found in macrophages by studying _______ bacteria in mice.
  20. Select organ failure from COVID-19 could be due to _____ expression
  21. Study quantified _____ cells as low risk
  22. An advantage of DNA Microarrays is _________
  23. Adaptor ligation prepares each ____ strand to ligate.
  24. Surprisingly, ______ cells had low ACE2 expression