Go Back   SEQanswers > Bioinformatics > Bioinformatics

Similar Threads
Thread Thread Starter Forum Replies Last Post
Remove Illumina TruSeq Index adapters enrico16 Bioinformatics 0 01-14-2015 12:56 AM
GS junior amplicon seq - remove adapters silvi 454 Pyrosequencing 10 03-04-2014 04:13 AM
fastx-clipper to remove adapters problem mihuzx Bioinformatics 0 11-11-2013 02:13 AM
Amplicon sequencing remove primer & adapters wzhang1001 Bioinformatics 4 07-19-2012 10:32 AM
Process to remove primers, adapters, etc. from Illumina data LizBent Bioinformatics 6 05-14-2012 04:08 AM

Thread Tools
Old 09-27-2016, 01:04 PM   #1
Junior Member
Location: Pacific Northwest

Join Date: Feb 2015
Posts: 1
Unhappy Can I remove index adapters after assembly?

I assembled a reference transcriptome de novo using Trinity with 2x300bp Illumina MiSeq PE reads. I used libraries from 4 individuals that were multiplexed over 4 lanes and chose "automated adapter trimming through the CASAVA pipeline." Assuming all of the adapters had been removed, I used a QC pipeline but skipped using 'scythe' to remove 3' end adapter contamination, assuming that these had been automatically trimmed when the samples were demultiplexed.

Since then, I have assembled and annotated the transcriptome (BLAST-style descriptions with usearch, protein prediction with InterProScan, mapped GO terms, etc.). However, as I attempted to upload the Transcriptome Shotgun Assembly (TSA) to NCBI, I received many error messages indicating that my assembly contained adapter contamination. Here is an example of the output:

File: pinus.albicaulis_transcriptome_tsa_v1.fsa, Code(VECTOR_MATCH), Sequence-id: TR2-c2_g1_i1, Interval: 2159..2224, This sequence has a Strong match on the following UniVec vector: gnl|uv|NGB00870.1:1-66 NEBNext Index 27 Primer for Illumina

[My library preparation used TruSeq LT kit which apparently is the same]

After looking into it, it seems that flagged transcripts do indeed have 3' end index adapter contamination and some have AAAAA tails afterward. Of course, I cannot upload the TSA without solving this problem.

Is there any way to simply trim adapter contamination from the completed reference transcriptome .fasta file? Many of the contaminated assembled sequences are even annotated and it seems these adapter sequences are present in their full form. I know adapter trimming programs generally require .fastq quality information, but I'm really hoping there may be an alternative to starting over again from the raw read data.

Is this a massive setback? Will I need to redo everything from scratch? Thanks for any help in advance.
Whitebark is offline   Reply With Quote
Old 09-27-2016, 09:11 PM   #2
Location: Antwerp, Belgium

Join Date: Oct 2015
Posts: 97

There probably is no good way to solve this from the assembly, this really has to be done at the beginning. Moreover, I would suspect that having adapter sequences present in your reads could lead to spurious assemblies, i.e., errors. You definitely want to avoid those right?
wdecoster is offline   Reply With Quote

adapter, assembly, illumina, trimming, truseq

Thread Tools

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off

All times are GMT -8. The time now is 05:17 AM.

Powered by vBulletin® Version 3.8.9
Copyright ©2000 - 2021, vBulletin Solutions, Inc.
Single Sign On provided by vBSSO