Hello, I would like to ask you why TruSeq (http://www.illumina.com/products/by-...eq-rna-v2.html) favours moleculers longer than 200 bp?
Are circular RNAs visible after sequencing with this protocol?
Why small RNAs cannot be analysed after using TruSeq?
Will be really grateful for help, I cannot find the answers.
(For example usually there is done TruSeq and separately TruSeq Small RNAs and I do not catch idea behind it
)
Are circular RNAs visible after sequencing with this protocol?
Why small RNAs cannot be analysed after using TruSeq?
Will be really grateful for help, I cannot find the answers.
(For example usually there is done TruSeq and separately TruSeq Small RNAs and I do not catch idea behind it
)
