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Hello,
first of all thanks for this really useful tool! I have one BAM file with single nuclei data from 8 conditions. I run the isoquant like this:
isoquant.py --reference /path/Mus_musculus.GRCm39.dna.primary_assembly.fa.gz
--genedb path/Mus_musculus.GRCm39.112.gtf.gz --complete_genedb
--bam path/lib2.aligned.sorted.bam
--data_type 'nanopore'
--report_novel_unspliced true
-o path/isoquant_results
--sqanti_output
Can I split the results based on condition and barcode or should I split the bam files first?
Thank you in advance,
VK
The text was updated successfully, but these errors were encountered:
Could you please clarify, would you like to have a separate output for each condition, or an expression table with barcodes and conditions?
How are you barcodes and conditions are stored?
So far IsoQuant supports only one way of grouping reads via --read_group, so either by condition or by barcode. This can be done using a separate table, i.e. read-barcode table, or BAM file tags.
If you'd like to group by different criteria, unfortunately you have to run IsoQuant twice.
I am planning to implement multiple read grouping in the future.
Hello,
first of all thanks for this really useful tool! I have one BAM file with single nuclei data from 8 conditions. I run the isoquant like this:
isoquant.py --reference /path/Mus_musculus.GRCm39.dna.primary_assembly.fa.gz
--genedb path/Mus_musculus.GRCm39.112.gtf.gz --complete_genedb
--bam path/lib2.aligned.sorted.bam
--data_type 'nanopore'
--report_novel_unspliced true
-o path/isoquant_results
--sqanti_output
Can I split the results based on condition and barcode or should I split the bam files first?
Thank you in advance,
VK
The text was updated successfully, but these errors were encountered: