• 448
• 0

How do you get untrimmed reads from the sequencer?

• 464
• 0

What method of clustering do we use for the UMAP?

• 381
• 0

Do you have any guidance on trimming FASTQ files to 2 x 50?

• 373
• 0

How do I recalculate "median reads/UMI" after filtering out beads not covered by tissue?

• 477
• 0

What if my library has indications of PCR-bubble formation?

• 392
• 0

What is difference between the Dual Indexing primer kit V1 and V2?

• 552
• 0

Do you need to optimize the permeabilization step for Curio Seeker?

• 538
• 0

If I have low cDNA concentration, how do I re-amplify it?

• 327
• 0

Do I need to make any adjustments for running Human Heart tissue?

• 545
• 0

What modifications do I need to make for running Curio Seeker on plant tissue?

• 715
• 0

How do I harvest and preserve fresh frozen tissue for sectioning?

• 433
• 0

Is the use of the CryoCube essential? What if it is not used?

• 603
• 0

How do we use the CryoCube?

• 422
• 0

How long does the Curio Seeker workflow take?

• 293
• 0

Are there any special steps that need to be followed when loading a ThruPLEX DNA-Seq library onto a flow cell?

• 305
• 0

Is it recommended to spike PhiX into a ThruPLEX DNA-Seq library prior to loading onto a flow cell?

• 343
• 0

What concentration of ThruPLEX DNA-Seq library should be loaded onto a flow cell?

• 399
• 0

Are there any special considerations that must be taken into account when performing AMPure XP purification on libraries prepared with the ThruPLEX DNA-Seq Kit?