duplex-tools
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Splitting of sequence reads by internal adapter sequence search
Hi, I would like to clarify if you would recommend merging the final duplex bam files: duplex_orig.sam duplex_splitduplex.sam Thanks
Hi, I am trying to use the "split_on_adapter" functionality to split chimeric ONT reads into sub-reads. Since we are using different adapters and primers than the one specified in the...
Hi, I am trying to get duplex sequencing up but I find I get a very low number of 'good pairs' after filtering and consenquently, a very low number of...
When I try to run guppy_duplex on my fast5 files, it successfully completes simplex basecalling but then gives the error `ValueError: not enough values to unpack (expected 4, got 3)`...
I successfully ran split_on_adapter with the --allow-multiple-splits option and it split a bunch of reads for me. When converting the new mapped SAM file to BAM format, it wrote about...
When running: ``` $ duplex_tools --version Duplex Sequencing Tools 0.3.2 $ python --version Python 3.11.0 $ duplex_tools split_pairs --threads 2 dorado.moves.bam OESO_152_LSK114/20230322_1606_3G_PAO27011_7b4991d0/ OESO_152_LSK114_pod5s_splitduplex/ ``` I get the following exception: ```...
Hello, I extracted fastq from the duplex_orig.sam and compared output to the original raw reads. In the following alignment file, The top sequence is the output for the duplex read....
Since barcoding is still under development in darado, I was wondering what alternative approach would be a proper way to extract duplex reads for multiplexed samples? I am thinking along...
Hi I'm using duplex_tools filter_pairs (duplex tools version: 0.3.2) on promethion created fastq files and out of 2759916 duplex pairs none are reported good. I did find the issue where...
When running split pairs on pod5s and the basecalled sam, duplex tools generates a new folder with split pod5 files and associated read ids. Does this folder contain all the...