Softwares
Names | Stars & Forks | Issues | PRs | Downloads |
---|---|---|---|---|
pyCirclize | ||||
pyGenomeViz | ||||
pyMSAviz | ||||
ANIclustermap | ||||
COGclassifier | ||||
phyTreeViz | ||||
pybarrnap |
A tool for drawing ANI clustermap between all-vs-all microbial genomes
License: MIT License
Names | Stars & Forks | Issues | PRs | Downloads |
---|---|---|---|---|
pyCirclize | ||||
pyGenomeViz | ||||
pyMSAviz | ||||
ANIclustermap | ||||
COGclassifier | ||||
phyTreeViz | ||||
pybarrnap |
Hey, after long time of running the tool without problems, when running ANIclustermap I encountered now the following issue:
# Step1: Run fastani between all-vs-all 13 genomes.
dyld: Library not loaded: @rpath/libopenblasp-r0.3.7.dylib
Referenced from: /Users/leonidou/opt/anaconda3/envs/ANIclustermap/bin/fastANI
Reason: image not found
Traceback (most recent call last):
File "/Users/leonidou/opt/anaconda3/envs/ANIclustermap/bin/ANIclustermap", line 10, in <module>
sys.exit(main())
File "/Users/leonidou/opt/anaconda3/envs/ANIclustermap/lib/python3.8/site-packages/aniclustermap/aniclustermap.py", line 29, in main
run(**args.__dict__)
File "/Users/leonidou/opt/anaconda3/envs/ANIclustermap/lib/python3.8/site-packages/aniclustermap/aniclustermap.py", line 75, in run
ani_df = parse_ani_matrix(ani_matrix_file)
File "/Users/leonidou/opt/anaconda3/envs/ANIclustermap/lib/python3.8/site-packages/aniclustermap/aniclustermap.py", line 229, in parse_ani_matrix
with open(matrix_file) as f:
FileNotFoundError: [Errno 2] No such file or directory: 'ANIclustermap_Results/work/fastani_result.matrix'
It must be something with the dyld library that I was not able to fix.
The tool worked so far perfectly for me, and suddenly I get this error..Thanks in advance!
Dear all,
I have downloaded some strain assemblies (looking like files GCF_000014505.1_ASM1450v1_genomic.fna)
In the folder I have put my strain assembly fna file, but whatever name I give to my file it is not present in the png, and I see that workflow loads all files but mine (and I checked the fasta is fine)? Can you help?
Hey, when running ANIclustermap I encountered the following issues:
# Step1: Run fastANI between all-vs-all 7 genomes.
/bin/sh: fastANI: command not found
Traceback (most recent call last):
File "/Users/leonidou/opt/anaconda3/bin/ANIclustermap", line 8, in <module>
sys.exit(main())
File "/Users/leonidou/opt/anaconda3/lib/python3.8/site-packages/aniclustermap/aniclustermap.py", line 44, in main
run(
File "/Users/leonidou/opt/anaconda3/lib/python3.8/site-packages/aniclustermap/aniclustermap.py", line 93, in run
fastani_df = parse_fastani_matrix(fastani_matrix_file)
File "/Users/leonidou/opt/anaconda3/lib/python3.8/site-packages/aniclustermap/aniclustermap.py", line 231, in parse_fastani_matrix
with open(matrix_file) as f:
FileNotFoundError: [Errno 2] No such file or directory: 'Results/work/fastani_result.matrix'
Could you please help me how to resolve the issue? Many thanks in advance!
Is there a genome number limit? When I run it with 20-30genomes is fine, but when I input >50 I got error:
Traceback (most recent call last):
File "/Library/Frameworks/Python.framework/Versions/3.10/bin/ANIclustermap", line 8, in <module>
sys.exit(main())
File "/Library/Frameworks/Python.framework/Versions/3.10/lib/python3.10/site-packages/aniclustermap/aniclustermap.py", line 44, in main
run(
File "/Library/Frameworks/Python.framework/Versions/3.10/lib/python3.10/site-packages/aniclustermap/aniclustermap.py", line 93, in run
fastani_df = parse_fastani_matrix(fastani_matrix_file)
File "/Library/Frameworks/Python.framework/Versions/3.10/lib/python3.10/site-packages/aniclustermap/aniclustermap.py", line 231, in parse_fastani_matrix
with open(matrix_file) as f:
FileNotFoundError: [Errno 2] No such file or directory: 'pl_out2/work/fastani_result.matrix'
Hey, I came accross you piece when looking for a way to visulize the fastANI output. So I was wondering if it is possible to input an existing fastANI output into your ANIclustermap.
All the best,
Lisa
Hi,
Second issue to enhance this tools =)
Most People use differents tools for ANI score like OrthoANI or want to use AAI score or mash distance values, all theses tools produce a similarity matrix file.
Is it possible to bypass the FastANI step in your tool by directly passing the similarity matrix (tsv/csv format) ?
Thanks in advance for your work.
Have a good day.
Hi,
I am trying to run this tool and encountered this error
/bin/sh: fastANI: command not found
Traceback (most recent call last):
File "/Users/emmannaemeka/mambaforge/bin/ANIclustermap", line 8, in
sys.exit(main())
File "/Users/emmannaemeka/mambaforge/lib/python3.9/site-packages/aniclustermap/aniclustermap.py", line 29, in main
run(**args.dict)
File "/Users/emmannaemeka/mambaforge/lib/python3.9/site-packages/aniclustermap/aniclustermap.py", line 75, in run
ani_df = parse_ani_matrix(ani_matrix_file)
File "/Users/emmannaemeka/mambaforge/lib/python3.9/site-packages/aniclustermap/aniclustermap.py", line 229, in parse_ani_matrix
with open(matrix_file) as f:
FileNotFoundError: [Errno 2] No such file or directory: 'anicluster_map/work/fastani_result.matrix'
Hi,
Is it possible to have a special range color for taxonomist user or the possibility to define (by a configuration file) a range by color ?
For the taxonomist user, they like to have a color range of 100% ANI, 99%-95%, 94%-83%, 82%-70% and 70%-0%.
Thanks for your work.
Have a good day.
received the above error even when use example data
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