Question: Decreased base quality at start of RNA seq reads
0
gravatar for brismiller
2.3 years ago by
brismiller40
Bellingham, WA, USA
brismiller40 wrote:

Hey all,

While running quality control steps for an RNA-Seq experiment I can see a decrease in the read quality score at the first few nucleotides (see below). enter image description here

I read the fastQC manual and it said on the Per Base Sequence Quality that poor quality at the start of the run could be caused by bubbles in the flowcell. But with that said the per-tile quality plot looks fine.

Another possibility is that a warn / error is triggered because of a short loss of quality earlier in the run, which then recovers to produce later good quality sequence. This can happen if there is a transient problem with the run (bubbles passing through a flowcell for example). You can normally see this type of error by looking at the per-tile quality plot (if available for your platform). In these cases, trimming is not advisable as it will remove later good sequence, but you might want to consider masking bases during subsequent mapping or assembly.

Any thoughts?

ADD COMMENTlink modified 2.3 years ago by Wietje210 • written 2.3 years ago by brismiller40

Not sure about the root cause, but the data is still in the "good" range (phred score 30 - 40)

ADD REPLYlink written 2.3 years ago by lakhujanivijay5.2k
0
gravatar for Wietje
2.3 years ago by
Wietje210
Germany
Wietje210 wrote:

Take a look at this post and the answers that have been suggested - maybe this is of some help to you.

ADD COMMENTlink written 2.3 years ago by Wietje210
Please log in to add an answer.

Help
Access

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 2.3.0
Traffic: 1545 users visited in the last hour