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Thread | Thread Starter | Forum | Replies | Last Post |
Threshold quality score to determine the quality read of ILLUMINA reads problem | edge | Illumina/Solexa | 35 | 11-02-2015 11:31 AM |
Threshold quality score to determine the quality read of ILLUMINA reads problem | edge | General | 1 | 09-13-2010 03:22 PM |
Which quality score? | baohua100 | Bioinformatics | 2 | 03-28-2009 06:52 PM |
Fastq quliaty score and MAQ output quality score | baohua100 | Bioinformatics | 1 | 02-19-2009 10:21 AM |
Quality score graph | vruotti | Bioinformatics | 3 | 11-20-2008 02:06 PM |
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#1 |
Junior Member
Location: austria Join Date: Feb 2010
Posts: 2
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Hey!
I read something about 454 sequencing, but there are some things I don't understand. (http://www.nature.com/nature/journal...ture03959.html) Quality Score: Why is the quality score the probability, that a homopolymer of at least length n caused the signal, not exactly length n? And in the formula, the j-variable of the sum-symbol goes from n to infinity? Z-Score: If we need a reference sequence to calculate the Z-Score, we can only use it when resequencing a genome, not when we are doing a de novo assembly. In the supplementary methods it says it is also applicalbe when doing the de novo sequencing, but how? Just align the reads? And what is aligned, the peaks of the flowgrams? Furthermore, if the Z-Score is the difference between the averaged signal values of the different reads and the nearest integer, divided by the standard deviation of the read signals, wouldn't an averaged signal of e.g. 6.5 give rise to a higher Z-Score than an averaged signal of 6.9 when having the same standard deviation?? Or do I misinterpret the meaning of the Z-Score (confidence, that there is one particular base at a particular position)? Flow order: There appear two PPi Kernels during sequencing. Are they used to measure the amount of enzyme-beads and fragments (to correct the signal strength for each well)? Thanks, david |
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#2 | |
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Location: DK Join Date: Jan 2011
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Hi,
as far as I can tell, there must be an error in the quality score definition... In the link you provide above (http://www.nature.com/nature/journal...ture03959.html), Margulies et al. (2005) states that the quality score is: Q = -10 log10( P(≥n|s) ) where s is the observed signal and n is the length of the homopolymer that produced the signal. That would mean that: Q = 40 <=> P(≥n|s) = 0.0001 Q = 20 <=> P(≥n|s) = 0.01 So the probability that the homopolymer is of length ≥n is higher when the quality score is lower! That must be a mistake. How should one interpret the quality scores? Margulies (2005) writes: Quote:
Code:
Position: 1 2 3 4 5 6 7 8 9 10 11 Residue: T G G G A G G G G A T Quality: 30 27 30 30 28 14 14 13 13 19 20 a) position 2 has lower quality than the rest of the homopolymer? b) position 7 has higher quality than the rest of the homopolymer? Anybody know how the quality score is calculated (eg. sourcecode)? Cheers, T Last edited by TSR; 08-30-2011 at 05:05 AM. |
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#3 |
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Location: CA Join Date: Oct 2011
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Their formula and coding are fine.
Reported is the probability to their ERROR Model. |
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#4 |
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Location: canada Join Date: Oct 2020
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Thanks for sharing this much knowledge. This post taught us in a very good manner. I am really happy to read this.
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#5 |
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Location: bangalore Join Date: Oct 2020
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java training bangalorehttp://www.acte.in/java-training-in-bangalore Last edited by ragulbabu76; 10-15-2020 at 11:31 PM. Reason: error accuring |
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