Hi,
I'm analysing data from a multiplexed RNA-seq experiment where the library was generated using the Ilumina TruSeq Universal Adapter and the Illumina TruSeq Index Adapters (see page 12 of this letter from Illumina).
From the FastQC report I can see a slight adapter contamination and I'd like to remove all adapters from the FASTQ files before progressing with the analysis. I'm using Scythe, which needs the adpater sequences in FASTA format. This is my FASTA file:
>TruSeq_Universal_Adapter
AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT
>TruSeq_Universal_Adapter_RC
AGATCGGAAGAGCGTCGTGTAGGGAAAGAGTGTAGATCTCGGTGGTCGCCGTATCATT
>TruSeq_Index_Adapter
GATCGGAAGAGCACACGTCTGAACTCCAGTCAC
>TruSeq_Index_Adapter_RC
CAAGCAGAAGACGGCATACGAGAT
My questions are:
- For the index adapter, I'm using the invariable part of the sequence at the 5'- end of the 6 bases-long barcode (TruSeq_Index_Adapter) and the reverse complement of the sequence at the 3'- end of the 6-bases-long barcode (TruSeq_Index_Adapter_RC). Is this correct?
- Do I need to include the adapters' reverse complements at all or this is already taken care of when specifying the forward sequence?
Thanks!
Hello Enrico!
It appears that your post has been cross-posted to another site: SEQanswers.
This is typically not recommended as it runs the risk of annoying people in both communities.
Hi Devon,
Sorry, I had no idea this was an issue! Should I remove the SEQanswers one?
I'm not sure that you can. Just keep that in mind in the future.
I have same question as OP; Thus: What would be the post on SEQanswers?
I am looking for answers to the same question but not able to find this question at SEQanswers. Can you direct me to the post?
Here is the letter with Illumina adapter sequences.