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  3. Seeker

Seeker

62 Articles
  • 299
  • 0

What do I do if the FORMATCONVERT step fails with the following error?

  • 329
  • 0

CURIOSEEKER_GEN_GENE_BARCODE_UMI_DB step failed with the following error. How do I resolve it?

  • 315
  • 0

If I have multiple regions or tissues of interest on a tile, how do I select only the beads for the region I am interested in?

  • 321
  • 0

How do you get untrimmed reads from the sequencer?

  • 349
  • 0

What method of clustering do we use for the UMAP?

  • 233
  • 0

What is the conversion of coordinate system to um?

  • 283
  • 0

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

  • 295
  • 0

What are the minimum system requirements for local installation of the Curio primary analysis pipeline?

  • 276
  • 0

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

  • 324
  • 0

How do I filter out the background in the sample?

  • 333
  • 0

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

  • 302
  • 0

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

  • 429
  • 0

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

  • 384
  • 0

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

  • 245
  • 0

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

  • 395
  • 0

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

  • 547
  • 0

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

  • 322
  • 0

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

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