Hi All,
I'm currently using the Lib-L kit for GS Junior. My PCR product size is around 500 bp, but I've been having trouble getting sequence reads with that length...After the sequencing run, I saw several read length distributions, for example, a peak at 150 bp, 300 bp, 400 bp, and 500 bp. Previously, I've also seen other samples that had two peaks, around 400 and 500 bp. These were all done with shot gun processing - so when I convert the raw data from shot gun to amplicon sequencing, I could still get enough sequences for analysis, but I'd like to resolve the issue since our lab has been using shot gun processing. Is there any step in the library prep I should be aware of to improve my read lengths? Size check with flashgel after ligation step indicated that I did have the correct fragment size.
Thanks for your help!
I'm currently using the Lib-L kit for GS Junior. My PCR product size is around 500 bp, but I've been having trouble getting sequence reads with that length...After the sequencing run, I saw several read length distributions, for example, a peak at 150 bp, 300 bp, 400 bp, and 500 bp. Previously, I've also seen other samples that had two peaks, around 400 and 500 bp. These were all done with shot gun processing - so when I convert the raw data from shot gun to amplicon sequencing, I could still get enough sequences for analysis, but I'd like to resolve the issue since our lab has been using shot gun processing. Is there any step in the library prep I should be aware of to improve my read lengths? Size check with flashgel after ligation step indicated that I did have the correct fragment size.
Thanks for your help!
Comment