Does the barcode filter in bbduk.sh (v37.66) only allow perfect matches or are mismatches allowed?
Thanks,
Lynn
Thanks,
Lynn
-
-
What barcode filter are you referring? Generally with "hdist=N" paramter you can allow or disallow (hdist=0) mismatches. -
I'm referring to these parameters:
barcodefilter=t barcodes=TCTCGCGC
As far as I can see from my results right now, only reads with exactly this sequence in the header are retained. I think this may be too stringent. Does the 'hdist' parameter affect the barcode given how short it is?Comment
-
I see. I have not personally used this feature since most of barcode work is done at the bcl2fastq stage, where you can allow for errors in sequence.
What exactly are you trying to do? Eliminate reads with some barcodes? I don't think the hdist= parameter is going to apply for the barcodes. It is for errors in the main read. You may have to look for an alternate way to do this. Perhaps using "demuxbyname.sh" may be a better option. Take a look at that.Comment
-
Thanks for the reply. I have a set of large paired-end fastq files that were preprocessed by a sequencing core and I suspect that they were never demultiplexed because the file is quite large and may have had its own lane or flowcell. The headers contain barcodes that are mostly TCTCGCGC or that string with one or two mismatches but there are also barcodes that are wildly different and I want to strip those out without stripping what are probably legit barcodes with 1 or 2 mismatches. When I tried demuxbyname.sh, it started writing out 2x80,000 files, two for every barcode variant present.Comment
-
Use the code I have in this post to enumerate all the different barcodes present in your file. That should give you an idea of the complexity of the problem. Then choose the ones you want (that actually should belong to your samples since you made them) to demux and use only those with demuxbyname.sh.Comment
-
I have already looked at all the barcodes. I've got 76,959 different barcodes that are not exact matches accounting for about 48 million reads. If allow 1 mismatch, I could recover 16 million of those. If I allow 2 mismatches, I could recover 24 million.Comment
-
I wrote a perl script using the fuzzy match module (Text::Fuzzy) to pull all the entries with no more than two mismatches in the barcode. It's not much but I can send to anyone who is interested.Comment
-
In future just ask the sequence provider to re-do the demultiplexing with bcl2fastq. You are paying them for it anyway :-)Comment
-
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...10-14-2026, 09:55 AM -
Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.
We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing...
Comment