Base Quality
1 - What is the last read in the SRR2584863_1.fastq
file? How confident
are you in this read?
File Size
2 - How big are the files?
(Hint: Look at the options for the ls
command to see how to show
file sizes.)
Overall Read Quality
3 - Which sample(s) looks the best in terms of per base sequence quality? Which sample(s) look the worst?
FastQC
4 - Which samples failed at least one of FastQC’s quality tests? What test(s) did those samples fail?
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