Checkpoint: reads extraction - aechchiki/SIB_LongReadsWorkshop_Zurich17 GitHub Wiki
Reads extraction: MinION
You should be able to answer these questions if you successfully completed tutorial Extraction of MinION reads .
-
Are you familiar with the fastq format? What does each line correspond to? Hint
-
What are the other utilities embedded in the
poretools
toolkit? Hint -
How many reads are in your dataset? Hint
-
How would you change the command line if you wanted to only extract the reads corresponding to a high quality subset of the 2D reads? Are there any 2D reads with no complementary template/complement? How are the 2D reads generated? Hint
-
Choose a 2D read at random. Look for the corresponding reads in 1D (template/complement). Do you see an improvement in the quality scores? Hint
Reads extraction: PacBio
You should be able to answer these questions if you successfully completed tutorial Extraction of PacBio reads subsection.
-
How many reads are in your dataset? From how many flowcells?
-
How are these reads called according to the PacBio terminology? Hint
Next
Go to next section Genome assembly .
Go back to Table of content .