Closed crutching closed 6 years ago
We recently developed a variant of BAMClipper to handle single primer extension dataset but I am not sure whether it fits your dataset. Is your dataset based on a commercially available gene panel like Qiagen Qiaseq? or ArcherDx?
Great, I'd love to try it out! Otherwise, I will be writing my own. Yes, this is based on the QIAseq method, with UMIs. I'm feeling good about adapter and UMI handling, now just trying to deal with the error rate in primer regions leading to incorrect allele frequency estimation.
We would also like to test it. Is it possible ?
Please contact chau@hksh.com for further discussion. Thank you.
Hi there,
I'm curious about paired-end designs utilizing a single primer. Is this something that BamClipper can handle?
Thanks!