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TraCeR on 10X cellranegr vdj output filtered_contig.fasta demultiplexed files #95

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arutik opened this issue Oct 15, 2019 · 8 comments

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@arutik
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arutik commented Oct 15, 2019

Hi,

Similar to this issue Teichlab/bracer#21 (comment) in BraCeR, can one run TraCeR on the per-cell fasta files demultiplexed from filtered_contig.fasta output of cellranger vdj?
If yes, then with what adjustments?

Thank you.

@mstubb
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mstubb commented Oct 15, 2019

Yes, I think that should enable you to get the files through TraCeR (although I've not tried it). Is there a reason you want to do that rather than using the Cell Ranger annotations?

@arutik
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arutik commented Oct 15, 2019

Thank you!

I first wanted to do this for BraCeR because I find BraCeR output data more comprehensive (for example, cellranger vdj doesn't output Ig isotype distribution or I can't find it) so I assumed the same would apply to TraCeR vs cellranger vdj, but I guess here there should be no major difference... or is there any TraCeR-specific output?

@mstubb
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mstubb commented Oct 15, 2019 via email

@arutik
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arutik commented Oct 15, 2019

Thanks a lot! This helps.

Sincerely,
Anna Arutyunyan

@arutik
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arutik commented Oct 20, 2019

Hi,

Coming back to the previous discussion, do you know if cellranger vdj reports CDR3 region sequences like TraCeR and BraCeR do?

Thank you.

Sincerely,
Anna Arutyunyan

@mstubb
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mstubb commented Oct 20, 2019 via email

@arutik
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arutik commented Oct 20, 2019

Thank you very much Mike!

Sincerely,
Anna Arutyunyan

@korakusa
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korakusa commented Feb 3, 2020

Hi,
I also would like to run TraCer with 10x genomics data (filtered_contig.fasta output of cellranger vdj) because I'm so interested in TraCer clonotype network graph.
I referred to Teichlab/bracer#21 and split my fasta file.
But in TraCer, there is no --assembled_file option.
How could I run tracer assemble with my fasta files? Should I submit them as a single-end sequencing?

Sincerely,
Sakurako

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