I tried to process my FASTQ files with UMI length 9 instead of 10 (10xv2) or 12 (10xv3).
R1: 25 --> 16 barcode and 9 UMI
R2: 50
To do so, I added a chemistry. However, I faced the following error message:
simpleaf add-chemistry --name honey --geometry 1{b[16]u[9]x:}2{r:}
2024-11-08T09:40:10.563033Z INFO simpleaf::simpleaf_commands::chemistry: inserting chemistry honey with geometry 1{b[16]u[9]x:}2{r:}
Error: Cannot automatically obtain an unfiltered permit list for non-Chromium chemistry : 1{b[16]u[9]x:}2{r:}
Instead of using the --unfiltered-pl, I should have used --knee.
While this resolves the add-chemistry error, I still could not align my FASTQ files.
Error: piscem mapping failed with exit status ExitStatus(unix_wait_status(134))
Instead of using a piscem-based index, I should have created an salmon-based index, which can be created by using the option --no-piscem in the simpleaf index command.
I tried to process my FASTQ files with UMI length 9 instead of 10 (10xv2) or 12 (10xv3).
R1: 25 --> 16 barcode and 9 UMI R2: 50
To do so, I added a chemistry. However, I faced the following error message:
Instead of using the
--unfiltered-pl
, I should have used--knee
.While this resolves the add-chemistry error, I still could not align my FASTQ files.
Instead of using a piscem-based index, I should have created an salmon-based index, which can be created by using the option
--no-piscem
in thesimpleaf index
command.