Unconfigured Ad
Collapse
X
-
yeah, thanks for that. the sequencing group here also pointed that out to me (I should have posted a followup). so now i am doing some real QC.... (but i still still think the data quality might be a bit low)
-
Due to the way the Illumina pipeline (or RTA) sorts the output to FASTQ files the reads at the beginning of the file always look bad. A FASTQ file for a lane of GAII data will have the reads sorted first by tile # and then by x-coordinate. Thus at the start of the file (or really at the start of every block of reads for each tile) you will have reads from the extreme edge of the tile. Reads at the edge are inherently poorer quality. You can't make any assessment about the overall quality of the run by looking at a few, non-randomly selected reads.Originally posted by maubp View PostHaving the quality scores drop off with the read length is normal. I haven't seen enough data to say for sure, but scores like yours do look worse the normal. Ask your sequencing centre to have a look at it maybe? Perhaps they had a bad run.
The reads at the top of my FASTQ files always have Q-scores like the ones shown here.
Leave a comment:
-
Having the quality scores drop off with the read length is normal. I haven't seen enough data to say for sure, but scores like yours do look worse the normal. Ask your sequencing centre to have a look at it maybe? Perhaps they had a bad run.
Leave a comment:
-
uuggh
that is what i feared. and I assume this is, in general, worse that what people usually get in their Illumina data?
Leave a comment:
-
The ASCII code for B is 66, with an offset of 64 as used in Solexa/Illumina gives a quality score of 2 (very poor).Originally posted by chrisbala View Postthanks. that is good to know...
any thoughts about the Bs???
At the start of the reads you have things like X, which is ASCII 88, thus a score of 24, which is OK.
i.e. The start of your reads have OK scores, but this rapidly trails off and the middle and ends of your reads have poor scores.
So yes, you did have the score interpretation backwards in your earlier posts.
[I'm assuming you have Solexa or Illumina style FASTQ files here]
Leave a comment:
-
You can avoid this by putting [ code ] and [ /code ] tags round the example. There is a little icon with a # symbol on it on the edit box to make this easy.Originally posted by Zigster View Posti assume the spaces i see in your sequences is an artifact of copy-paste?
Leave a comment:
-
spaces
thanks for the responses
yes the space is a copy-paste thing
also, i thought I did understand the quality scores ... just checking that I am correct in my understanding ... but I think I got it .. I had the quality scores backwards ... so Bs are actually quite bad reads? Much of my data looks like what I posted. Is this about what is expected?
Leave a comment:
-
i assume the spaces i see in your sequences is an artifact of copy-paste?
Leave a comment:
-
maybe handy to first read this paper in order to know what is what:
The Sanger FASTQ file format for sequences with quality scores, and the Solexa/Illumina FASTQ variants
Cock et al, 2009
Published in NAR
Leave a comment:
-
If you map human reads to human, good aligners can map 95% of them. If you align these reads to chimpanzee, which is 1.2-1.3% different from human, about 90% can be mapped. If you are talking about 5-10% mismatching rate, most short aligners would not work well. Perhaps ssaha2 is less affected. In addition, bowtie does not do gapped alignment. Also tuning bowtie "-e" may help. Alternatively, you may consider to de novo assemble your reads first and then align the contigs.
Leave a comment:
-
quality scores, low mapped%?
Hi,
I'm trying to figure out why I am getting such a low % of mapped reads (using tophat/bowtie). I'm still experimenting with parameters in bowtie, but thus far, I can't get much above 30%. I'm working with a new genome with plenty of gaps and things, so that might explain part of it. BUt I also don't fully understand the quality scores. Do these look funny to any of you? It seems to be the higher quality scores are on the end of these reads? (the Bs?). Any thoughts?
@HWI-EAS385_0044:2:1:4:1884#0/1
CAGCTGGNAGGCTCCACGGCGGGCGTGCGCCAAGTGCCGGGGCTGCACAACGGGAGCCAAGCCTTCCTCTTCTCA
+HWI-EAS385_0044:2:1:4:1884#0/1
\\X[\LTDTT_Vb__X_Z_V`XUceZcfcc_PTPKVb__\]bee]]X_BBBBBBBBBBBBBBBBBBBBBBBBBBB
@HWI-EAS385_0044:2:1:4:1477#0/1
GGGCCATNGCATCTGTGGGCACGGGAGGGGCCAGCACAGCCGCAGGACTACTGGCCGAGGCCCCCGCCGCGGCAG
+HWI-EAS385_0044:2:1:4:1477#0/1
ecdce[bE]`TTTSS\Wb\bTW^XNRMURVO\PX]Q`N^^R]SK\\\MVM\P\V^M[LPX`^BBBBBBBBBBBBB
@HWI-EAS385_0044:2:1:4:849#0/1
GTCGTACTCCTAGGGCTCGTGGTCGGCTGCGCCGGCTTGTCGTTTCGCTTCGCCTGCGGGCTGGGCTCCGTCGTG
+HWI-EAS385_0044:2:1:4:849#0/1
bXb_[`c_cc\U`BBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBTags: None
Latest Articles
Collapse
-
by SEQadmin2
Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?
Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating...-
Channel: Articles
10-14-2026, 09:55 AM -
ad_right_rmr
Collapse
News
Collapse
| Topics | Statistics | Last Post | ||
|---|---|---|---|---|
|
Genome Sequencing Reveals Large, Repeat-Rich DNA in Trapdoor Spider Named for Stephen Colbert
by SEQadmin2
Started by SEQadmin2, 10-28-2026, 09:57 AM
|
0 responses
22 views
0 reactions
|
Last Post
by SEQadmin2
10-28-2026, 09:57 AM
|
||
|
Started by SEQadmin2, 10-28-2026, 09:51 AM
|
0 responses
14 views
0 reactions
|
Last Post
by SEQadmin2
10-28-2026, 09:51 AM
|
||
|
Started by SEQadmin2, 10-22-2026, 11:13 AM
|
0 responses
67 views
0 reactions
|
Last Post
by SEQadmin2
10-22-2026, 11:13 AM
|
||
|
Started by SEQadmin2, 10-22-2026, 10:48 AM
|
0 responses
47 views
0 reactions
|
Last Post
by SEQadmin2
10-22-2026, 10:48 AM
|
Leave a comment: