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I try to use EHDn to detect tandem repeats in our samples. These samples were sequenced from PCR-based libraries (2 × 100 bp paired-end reads) , which were different from the data (2 × 150 bp paired-end reads from PCR-free samples) in the published article (Trost et al, 2020). And they detected more apparent tandem repeats in samples sequenced from PCR-based libraries.
This phenomenon is also observed in our data, the 150bp PE (PCR-free) data of the same sample detected less tandem repeats than the 100bp PE (PCR-based) reads (2909 vs 811). We are very confused about this issue.
I noticed that you mentioned in your introduction that short (100-200bp) sequencing data is suitable, but I'm still not sure if we can try to analyse these data (100PE, PCR-based). What do you think may be the reason for this difference? We would be very grateful if you could give us some advice.
Thanks in advance.
The text was updated successfully, but these errors were encountered:
Hi! Thank you for developing this tool.
I try to use EHDn to detect tandem repeats in our samples. These samples were sequenced from PCR-based libraries (2 × 100 bp paired-end reads) , which were different from the data (2 × 150 bp paired-end reads from PCR-free samples) in the published article (Trost et al, 2020). And they detected more apparent tandem repeats in samples sequenced from PCR-based libraries.
This phenomenon is also observed in our data, the 150bp PE (PCR-free) data of the same sample detected less tandem repeats than the 100bp PE (PCR-based) reads (2909 vs 811). We are very confused about this issue.
I noticed that you mentioned in your introduction that short (100-200bp) sequencing data is suitable, but I'm still not sure if we can try to analyse these data (100PE, PCR-based). What do you think may be the reason for this difference? We would be very grateful if you could give us some advice.
Thanks in advance.
The text was updated successfully, but these errors were encountered: