Comments (2)
Hello,
You're welcome (and thanks)!
There's no option for D genes because it doesn't really make a difference to stitchr. In a rearranged receptor all of the D gene residues are wholly contained inside the CDR3, so when you give stitchr the CDR3 it already has all the D sequence included.
(Just for the record the TRBD alleles do differ slightly. However they're very short and often pretty nibbled during VDJ recombination so it's often impossible to tell which was used - hence why D gene assignment isn't as much of a thing in TCR research like it is for BCRs.)
Cheers,
Jamie
from stitchr.
Thank you so much for the fast reply! It is very clear!
from stitchr.
Related Issues (20)
- Simplifying output / silent mode HOT 1
- J/C region broken in certain genes in skip/extra gene mode HOT 1
- Lower case CDR3 amino acid characters cause an error HOT 1
- TRDV2 error HOT 2
- Possible to use custom species (non-human/non-mouse)? HOT 1
- Alternative non-templated codon usage?
- Improve % of perfectly replicated CDR3s when using a NT CDR3
- Add -cite option to stitchr
- thimble function gives an error for LEADER sequence when stitching TCR HOT 3
- Compatibility of stitchr with Windows HOT 5
- CDR1/2 HOT 2
- Wild card usage in Thimble ignores extra genes (-xg/additional-genes.fasta)
- First example at https://jamieheather.github.io/stitchr/installation.html not working as expected HOT 2
- Importing stitchr for use in other scripts - obtain stitched aa sequence without C region information HOT 5
- Specify databases location HOT 5
- Add option to read FASTA automatically into additional-genes.fasta
- Add more details to docs about different error/warning messages HOT 1
- Integration with tidytcells HOT 4
- A issue about stitching immunoglobulins HOT 1
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from stitchr.