Hello everyone, I am new to the Seqanswers forum and NGS library preparation. I have prepared a library for WGS of 55 M.tb samples using Illumina DNA prep. All the samples were normalized so that the total DNA input is 100ng per sample and the protocol mentioned in the reference guide was followed as such. After library prep, tape station was performed for 16 samples using D1000 kit. The following are the qubit concentrations and tapestation results. It Would be helpful if anyone could help me interpret the data, whether I can proceed to pool all the samples and submit them for sequencing. The lab we will be outsourcing to will perform the sequencing in Novaseq 6000.
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Illumina DNA prep Library preparation and Normalization trouble shooting
Last edited by Praveenebenezer; 08-07-2024, 09:06 PM.Tags: None
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Hi callahank, thanks for the reply. Traces can be found in the attached PDF tapestation_traces_0508.pdf
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