8 results in 0.0028 seconds.
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Cleaning up ~12,000 bp product
I need to clean a ligated product of ~12,000 bp which I will be using for long read sequencing. Which cleaning bead should I use? Can SPRIselect beads... -
HMW tail in the library. Remove or leave and sequence?
Hi there,
Skipping all the suffering.. I now have my libraries for ChIPs-Seq: good looking peaks, but also a high molecular weight something on... -
Low DNA yield after adapter ligation
Hi guys,
I am generating RRBS library recently. In the whole process I use Beckman Ampure Xp beads to purify (cleanup and elute) DNA. But... -
Use library in Deconseq to remove human genome
Hello,
I am using Deconseq to remove human sequences from fastq files generated by Myseq Illumina. I created the database with the human... -
High peak at 240nm in libraries - does it matter?
Dear community,
I need some help, as RNA-sequencing is quite new for me...
I prepared DNA libraries from RNA for sequencing with illumina.... -
SPRI selection at high temperature or with denaturants for ssDNA?
Hi all,
I've heard that SPRI beads also work for ssDNA, and I'd like to do a SPRI bead size selection of ssDNA > 150 nt (for various... -
Ampure bead clean up
Hello,
How much drying time do you normally allow when using ampure beads XP to clean up your library preps?
I've been using the... -
Removing Adapter Dimers with AMPure Beads
Can someone help?
I have adapter dimmers or some other contaminant below 200 (probably 170bp). Ultimately, my goal is to remove the contaminates...
