ycl6 / 16S-rDNA-V3-V4

16S rDNA V3-V4 amplicon sequencing analysis using dada2, phyloseq, LEfSe, picrust2 and other tools. Demo: https://ycl6.github.io/16S-Demo/
GNU General Public License v3.0
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about dada2 filterandTrim parameter #3

Closed chulghim closed 4 years ago

chulghim commented 4 years ago

Can i get how to determine dada2 filterAndTrim() paramer? (truncLen=c(240,230), minLen=200, maxN=0, truncQ=2, maxEE=c(2,5) ..)

For example: Illuminia MiSeq - (2*250bp reads) 321F: TAATTCGTCCTACGGRAGGCAG 800R: AGCCGGACTACCRGGGTAT

I am curious if there is any formula.

ycl6 commented 4 years ago

There isn't a formula I'm afriad. The paramter you would most likely need to alter from the default values is truncLen. You need to inspect the quality plot that you generate with plotQualityProfile to judge how many bases you would keep and at the same time not truncating the reads too much and end up unable to merge majority of the paired read, i.e. you need to have a general idea of what's the length distribution of your amplicons

chulghim commented 4 years ago

Thank you very much. That's what i want to know.

Best regards, Namchul.

2020년 8월 10일 (월) 오후 5:19, I-Hsuan Lin notifications@github.com님이 작성:

There isn't a formula I'm afriad. The paramter you would most likely need to alter from the default values is truncLen. You need to inspect the quality plot that you generate with plotQualityProfile to judge how many bases you would keep and at the same time not truncating the reads too much and end up unable to merge majority of the paired read, i.e. you need to have a general idea of what's the length distribution of your amplicons

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ycl6 commented 4 years ago

@chulghim Glad to help, I'll close this for now