Hi all,
Sorry for the two frequent posts in a row.
I have paired-end RNA-Seq data generated from Illumina GA as well as HiSeq. I obtained this data from SRA (NCBI).
I am not sure if adapter trimming is a regular practice (must-do) before I can go for the reference genome alignment of these reads.
How would I know if I needed adapter trimming?
Thanks
Sorry for the two frequent posts in a row.
I have paired-end RNA-Seq data generated from Illumina GA as well as HiSeq. I obtained this data from SRA (NCBI).
I am not sure if adapter trimming is a regular practice (must-do) before I can go for the reference genome alignment of these reads.
How would I know if I needed adapter trimming?
Thanks
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