BD Rhapsody + Nanopore Sequencing #1709
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skyng22003
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Hi, which BD protocol did you use to generate the data? Also do you have ONT adapters trimmed from the FASTQ reads? I can create a custom preset for your dataset but it would help if you can share a subsample of reads from the original fastq file for me to test. You can write us at support@milaboratories.com. |
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Would it be possible to modify the "generic-ont-with-umi" protocol to include the BD Rhapsody Cell barcodes for TCR / mRNA analysis?
Thanks,
Sky
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