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View Code? Open in Web Editor NEWSynthego ICE - Inference of CRISPR Editing software
License: Other
Synthego ICE - Inference of CRISPR Editing software
License: Other
I get the error in the title. I dont see it listed exactly the same way in the websites troubleshooting guide. The wording is a little weird so Im wondering if its just some small grammar error in the command line version and it really is the error as listed on website (link below) or it actually means something different.
https://www.synthego.com/help/ice-error-control-ab1-trace-quality-scores-too-low-
I did not find a way to increase the maximum indel size in the site or as an option in the command line version. I am interested in deletions generally longer than 50bp (TIDE's maximum) but perhaps as long as a few hundred bases. Is this something ICE is programmed to handle?
Hi there,
we've been using synthego/ice:latest for over 10 months. It's been working well till last week when we did a docker pull and got a new image. All the runs failed with the same python error, and I can reproduce it running test_analysis.py:
E TypeError: ord() expected string of length 1, but int found
ice/classes/sanger_object.py:112: TypeError
The test env is
platform darwin -- Python 3.6.4, pytest-3.4.2, py-1.8.0, pluggy-0.6.0
Now we rolled back to an old image we saved before. But would like to report this bug in case it was overlooked.
Thanks,
Pei
docker pull synthego/ice
Cannot connect to the Docker daemon at unix:///var/run/docker.sock. Is the docker daemon running?
Thanks
Hi there,
one of our recent runs got this error "Control ab1 trace quality too upstream of guide too low", maybe it can be better worded. I am not sure if this is a data issue or a design issue?
Thanks,
Pei
i got it working,
can you share the part to make the graphics like you have in the web server
from contrib.txt
thanks
Hi, I am pretty new to data analysis on gene editing. I have successfully run the code and got the results. But I wonder how should I visualize the result?
Hello,
It is essential that I run a prior version to validate prior results. Please advise on the pytest failure, also observed in treatment data. Thanks.
-------------------------------------------------- analyzing 8 donor_no_alignment AAGTGCAGCTCGTCCGGCGT
Base dir: /tmp/tmpxqi1g4d4/batch_analysis
Single Sanger analysis failed ord() expected string of length 1, but int found
Traceback (most recent call last):
File "/home/tdfyoder/GIT/ice_v1.X/ice/ice/analysis.py", line 186, in multiple_sanger_analysis
result = single_sanger_analysis(*job_args, **job_kwargs)
File "/home/tdfyoder/GIT/ice_v1.X/ice/ice/analysis.py", line 77, in single_sanger_analysis
donor=donor)
File "/home/tdfyoder/GIT/ice_v1.X/ice/ice/classes/sanger_analysis.py", line 126, in initialize_with
control_sample.initialize_from_path(control_path)
File "/home/tdfyoder/GIT/ice_v1.X/ice/ice/classes/sanger_object.py", line 80, in initialize_from_path
phred_scores.append(ord(c))
TypeError: ord() expected string of length 1, but int found
None of the samples were able to be analyzed
False
===================================== 14 failed, 31 passed in 1.82 seconds ======================================
There is an typo in the Readme file describing installation:
pip install sythego_ice
should be
pip install synthego_ice
Putting this as a new feature request or question, as a lot of our users are asking for it.
In knockin experiments scientists want to check the actual inserted sequence. Are there any plans to have that in results instead of just a sequence of Ns?
Hi Thanks for sharing this tool.
After installation when running the example I get the following error:
$ synthego_ice --control ./ice/tests/test_data/good_example_control.ab1 --edited ./ice/tests/test_data/good_example_edited.ab1 --target AACCAGTTGCAGGCGCCCCA --out results/testing --verbose
Synthego ICE (https://synthego.com)
Version: 1.1.1-alpha1
Base dir: /rhampseq/kkiaee/ice/ice/results
Exception Caught!
Traceback (most recent call last):
File "/home/ccadmin/anaconda3/envs/ice_env/lib/python3.8/site-packages/ice/analysis.py", line 82, in single_sanger_analysis
sa.analyze_sample()
File "/home/ccadmin/anaconda3/envs/ice_env/lib/python3.8/site-packages/ice/classes/sanger_analysis.py", line 799, in analyze_sample
alignment.align_all()
File "/home/ccadmin/anaconda3/envs/ice_env/lib/python3.8/site-packages/ice/classes/pair_alignment.py", line 94, in align_all
self.all_aligned_clustal = self.align_list_to_clustal(aln, "control", "edited")
File "/home/ccadmin/anaconda3/envs/ice_env/lib/python3.8/site-packages/ice/classes/pair_alignment.py", line 80, in align_list_to_clustal
alignment_txt = aln_objs[0].format("clustal").split('\n', 2)[2]
AttributeError: 'MultipleSeqAlignment' object has no attribute 'format'
I'd appreciate your help in troubleshooting this.
Hi,
I am trying to extract the knockout score for a sample run as an individual sample. Can you please let me know which json file to parse?
Thanks
Hi there,
we recently encountered a problem running ICE (v1.2.0). See the error below:
Any idea what caused this?
Thanks,
Pei
Hi,
Can you please point me to the GitHub link for ICE v3?
Thanks
The sclearn package is deprecated. New package is scikit-learn. Change requirements.txt file to reflect new package name.
We want guide sequence searching to be case insensitive
I am currently running synthego-open/ice using the latest docker (I didn't want to explicitly use latest tag): synthego/ice:fix_throwing_out_wildtype_hdr. However, it looks as though the structure of the trace.json file differs from the structure of the trace.json file on your website. For example, when running a batch analysis using the docker version, the trace.json file looks as follows:
{
'ctrl_sample': {'trace_data': [], 'cutsite': #, 'guide_start': #, 'guide_end': #., 'pam_start': #, 'pam_end': #},
'edited_sample': {'trace_data': [], 'cutsite': #}
}
But when I run the same batch on your website and ask for the results back, the format looks as follows:
[
{
'ctrl_sample': {'trace_data': [], 'guide_target': {}, 'cutsites': [{}]}
'edited_sample': {'trace_data': [], 'cutsites': [{}]}
}
]
Am I doing something wrong to not recreate the same trace.json file? This is potentially problematic for me when trying to analyze multiplexed samples where the trace.json should be returned as a list with multiple cut sites.
Hi there,
we use ICE with docker install. It is very easy and fast to use, thanks!
I am curious what exactly the error was if a sample failed analysis. The log shows:
-- analyzing 40 filename.ab1 GGTGAGTGAGTGTGTGCGTG
analyzing 462 number of edit proposals
R_SQUARED 0.998049444356253
discord (aln window): 0.07 after cutsite: 0.13
Exception Caught!
None
I tried on your website, same "311" failed error. Just curious what that means.
Thanks again,
Pei
Dear ICE devs,
I just noticed python ice_analysis_single.py --version
says 1.2.0. Just curious what's been changed since v1.1.0?
Thanks,
Pei
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