Comments (1)
Hi @dierckxt, You are correct that CB2 currently only support case-control case, and this one would be tricky to apply with the current version. If you have any ideas to implement it, please share your thought.
Thank you,
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Related Issues (20)
- run_sgrna_quant fails HOT 3
- inconsistent between .fq.gz and .fastq? HOT 7
- calc_mappability HOT 1
- export join_count_and_design HOT 2
- plot_count_distribution add export option HOT 1
- gene_stat cpms HOT 2
- Clarity around logFC for gene_stats HOT 3
- Problem with gene-level statistic HOT 1
- Error in arising in run_sgrna_quant HOT 4
- How to handle paired-end fastqs HOT 5
- Cluster setup failed. 31 of 31 workers failed to connect. HOT 2
- run_sgrna_quant report the wrong sequences associated to sgRNA names HOT 2
- maximum guide length HOT 2
- Error in cb2_count() HOT 4
- Is it possible to analyze by inserting one mismatch guide RNA barcode? HOT 3
- Error in measure_gene_stats(sgrna_stat) HOT 3
- Fasta file issue HOT 16
- CB2 vhat estimation with variable total read count
- Choice of count normalisation
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