Output from fasta submission

[NicolasHipp]

Hi everyone,

I tested bracer on my single cell rna seq data. I used two approaches:
-used both paired fastq from 1 cell
The problem with this approach is that bracer recognize multiple BCR_recombinants, so It do not perform all the downstream analyses.
When I looked for the TPM of these 2 BCR_recombinant, I have one major BCR and a minor BCR (I assumed that the major clone is the right one).

-used fasta file of BCR generated with BASIC aligner
Bracer give me the same clone as the major represented one in the first approach, but when I looked in the output, I don't have the clonotype_sizes.pdf and clonotype_sizes.txt output

Is-it normal if I don't have these both outputs?

I'm also running BALDR on this dataset to confirm that the major clone is the good one.

Ps : Happy new year, thanks for this soft

[idalind]

Hi @NicolasHipp ,
Happy new year and thanks for the feedback! Did you run bracer summarise for just the one cell you tested, or for multiple cells?