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DNA barcode sequences for Qiime2 and meaning of it

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6.3 years ago

pple2202 • 0

Hi all

I'm newbie for metagenome analysis, Qiime2 and have been studying for days. I've searched a lot about DNA barcode sequence but there are several unsolved questions.

What does exactly DNA barcode sequence mean? As I know, DNA barcode sequences are for species identification so that when their DNA are sequenced, the specific DNA barcode sequences are attached right after the adapter. (5'-Adaptor-barcode sequence-fragment-adaptor-3'). Does this mean all of E.coli's sequenced file(fastq), for example, have same barcode sequence? Then what does the DNA barcode sequence mean used in metagenome sequencing? We don't know what species in sample.
How do I know whether barcode sequence is in fastq sequence file? Like, when I try to follow metagenome analysis process in dissertation and get data from ncbi, there is no barcode sequence file, only fastq sequence files even though the project is metagenome analysis.
It could be simple question. When I search for metagenome analysis in ncbi, there are a number of files named similar(e.g Bulk_soil.1, Bulk_soil.2, Bulk_soil.3 .....). What does this mean? Does this mean soil picked different times or location? Since there is no written detail of them.

Thanks

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ADD COMMENT • link updated 2.1 years ago by Ram 44k • written 6.3 years ago by pple2202 • 0

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Actually, barcodes are needed when your running multiple samples in one run of sequencing. These index sequences/barcode sequences used to identify which read is coming from which sample.
Generally, barcode sequences will be in the header of your .fastq file. The last segment of few nucleotides appended to the sequence header will be your barcode for that read. read more from qiimea
It depends on the experimental designing they have done. It could be 3 different places from where they have collected their samples or it could be soil from the same place with 3 different time points, or it could be same soil samples with 3 different treatment.

ADD REPLY • link 6.3 years ago by Nitin Narwade ★ 1.6k

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If I have the data demultiplexed, how can I do my metadata table if it has to have one label called: 'barcode'? Please answer. I will appreciate your answer.

ADD REPLY • link 2.1 years ago by Wendy • 0

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This link from Qiime2 doc should help. There are links for example metadata files if you scroll down on the page.

ADD REPLY • link 2.1 years ago by GenoMax 146k

score 0 · Answer 1 · 2018-07-11

DNA barcode used in metagenome sequencing is not for species identification, instead it is for distinguishing different samples run together in single sequencing run through the process of multiplexing. Means during library preparation, different barcodes (unique 6-8bp sequence) are added to each sample during library preparation and then they are pooled and sequences together (This process is known as multiplexing). Thus it helps in sequencing number of samples together in one go which results in exponential increase in the number of samples analysed in a single run, without drastically increasing sequencing cost and time. So after sequencing is completed, these all samples needs to be separate out. These separation is done by mean of barcode sequence added to each DNA fragment during library preparation, so that each read of particular sample is identified before the data analysis (This process is know as demultiplexing).

When you downloaded the data from NCBI, It was already demultiplexed based on the barcode information they carry in their sequence header.

Thus, when using split_libraries_fastq.py script in qiime, you can use parameter --barcode_type 'not-barcoded'