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I would like to see instructions for analysing CITE-seq data. For example, my data looks like
$ ls * CITE: BH_pool1_S1_L001_I1_001.fastq.gz BH_pool1_S1_L002_R1_001.fastq.gz BH_pool1_S1_L003_R2_001.fastq.gz BH_pool1_S1_L001_R1_001.fastq.gz BH_pool1_S1_L002_R2_001.fastq.gz BH_pool1_S1_L004_I1_001.fastq.gz BH_pool1_S1_L001_R2_001.fastq.gz BH_pool1_S1_L003_I1_001.fastq.gz BH_pool1_S1_L004_R1_001.fastq.gz BH_pool1_S1_L002_I1_001.fastq.gz BH_pool1_S1_L003_R1_001.fastq.gz BH_pool1_S1_L004_R2_001.fastq.gz GE3: BH_pool1_S1_L001_I1_001.fastq.gz BH_pool1_S1_L002_R1_001.fastq.gz BH_pool1_S1_L004_I1_001.fastq.gz BH_pool1_S1_L001_I2_001.fastq.gz BH_pool1_S1_L002_R2_001.fastq.gz BH_pool1_S1_L004_I2_001.fastq.gz BH_pool1_S1_L001_R1_001.fastq.gz BH_pool1_S1_L003_I1_001.fastq.gz BH_pool1_S1_L004_R1_001.fastq.gz BH_pool1_S1_L001_R2_001.fastq.gz BH_pool1_S1_L003_I2_001.fastq.gz BH_pool1_S1_L004_R2_001.fastq.gz BH_pool1_S1_L002_I1_001.fastq.gz BH_pool1_S1_L003_R1_001.fastq.gz BH_pool1_S1_L002_I2_001.fastq.gz BH_pool1_S1_L003_R2_001.fastq.gz
I wonder if Vireo can only process the GE3 folder and I need to write my own preprocessing for the CITE folder (matching cells).
The text was updated successfully, but these errors were encountered:
@DarioS did you ever figure this out?
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Vireo can only be applied to the RNA data on its own and then the user needs to write a cell barcode matching script for ADT.
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I would like to see instructions for analysing CITE-seq data. For example, my data looks like
I wonder if Vireo can only process the GE3 folder and I need to write my own preprocessing for the CITE folder (matching cells).
The text was updated successfully, but these errors were encountered: