Comments (13)
Thanks for the issue, I'll take a look. Probably after the weekend I have an answer for you
from seq2science.
Could you post what's in this file: /Users/u0107886/Stefanie/results/log/trackhub/ASM14944v2.index.log
On what kind of computer are you running it? Linux, Mac, or Windows?
from seq2science.
Thanks for your very quick response!! We are running it on a Mac, 4 cores. 32gb mom
from seq2science.
I can't reproduce the error, but I think it's because mac has a different version of grep than linux. Could you add grep to the environment that's needed for the trackhub index? That's file:
/Users/u0107886/miniconda/envs/seq2science/lib/python3.8/site-packages/seq2science/rules/../envs/ucsc.yaml
, and then add grep so that it looks like this:
name: ucsc
channels:
- conda-forge
- bioconda
- defaults
dependencies:
- bioconda::grep=3.4
- bioconda::ucsc-bedsort=377
- bioconda::ucsc-bedGraphToBigWig=377
- bioconda::ucsc-bedToBigBed=377
- bioconda::ucsc-fatotwobit=377
- bioconda::ucsc-gtftogenepred=377
- bioconda::ucsc-genepredtobed=377
- bioconda::ucsc-hggcpercent=377
- bioconda::ucsc-ixixx=377
- bioconda::ucsc-wigtobigwig=377
- conda-forge::conda-ecosystem-user-package-isolation=1.0
And then run seq2science as you normally would. It should re-install the environment, with GNU grep added, and hopefully this works then π!
Let me know if that solves the issue for you. As a last resort solution you can always set create_trackhub: false
so that no ucsc trackhub is made which hopefully run the rest of the pipeline successfully
from seq2science.
Hey! Thanks for that! I had to set the create_trackhub to false...
The workflow ran, but got stuck near the end...
I attached the error log.
seq2science.2022-12-22T101835.775224.log
from seq2science.
from seq2science.
Hey!
Thanks already for all your help!
to recap: Trackhub is still set to false,
deeptools_qc is also set to false. it then runs till the error attached below.
I looked for this error in previous issue mentions and found it here
#625
but I don't see what is changed to overcome this issue.
Kind regards,
Wouter
seq2science.2023-01-03T143400.407190.log
from seq2science.
Can you post the log of the actual rule that fails?
/Users/u0107886/Stefanie/results/log/combine_peaks/ASM14944v2-macs2.log
from seq2science.
Next time I'll immediately include that!
from seq2science.
That one I actually solved yesterday (I think). At the end of today there will be a new seq2science release. Hopefully everything works for you with that version
from seq2science.
You can try mamba install seq2science=0.9.7
tomorrow in your seq2science environment, and seq2science should be updated to the newest version. Please let me know if it works then π
from seq2science.
The issue you had was with conda and the newest numpy version. I've changed the description on which numpy version should be used on the bioconda side, so probably removing the environment and just restarting the run with the current seq2science version also works btw.
rm -r ../miniconda/envs/seq2science/lib/python3.8/site-packages/seq2science/.snakemake/cd6528626806a6e527f5cf7769376ea3_
seq2science run ...
from seq2science.
I'm assuming this has been resolved, feel free to reopen if not
from seq2science.
Related Issues (20)
- BUG: download_fastq report error HOT 4
- BUG: [config.yaml error] HOT 15
- Combining STAR and Salmon HOT 5
- STAR 2-pass alignment HOT 1
- Q: [Comparative RNA-Seq analysis] HOT 2
- Q: [DEG analysis contrast] HOT 1
- BUG: chipseeker is broken (again)
- FR: [DEG by Salmon]
- FR: python/scanpy interoperability for single cell?
- FR: single cell auto detection if droplet or cell based barcodes?
- BUG: qc_scRNA rules dont use params, so rerunning doesn't work
- FR: single cell RNA filtering
- Issue with Chip-seq pipeline: jobid: 27: one of the commands exited with non-zero exit code; note that snakemake uses bash strict mode! HOT 8
- BUG: Problem with the Initiation HOT 6
- FR: Use temporary directories for sra and temporary fastq files HOT 14
- BUG: Incorrect SRA files (RNA-seq) HOT 1
- BUG: [scATAC-seq successful run but bam file and snap object are missing cell barcodes] HOT 6
- FR: don't crash when no differential genes are found HOT 4
- BUG: latest numpy version and IDR inconsistency HOT 1
Recommend Projects
-
React
A declarative, efficient, and flexible JavaScript library for building user interfaces.
-
Vue.js
π Vue.js is a progressive, incrementally-adoptable JavaScript framework for building UI on the web.
-
Typescript
TypeScript is a superset of JavaScript that compiles to clean JavaScript output.
-
TensorFlow
An Open Source Machine Learning Framework for Everyone
-
Django
The Web framework for perfectionists with deadlines.
-
Laravel
A PHP framework for web artisans
-
D3
Bring data to life with SVG, Canvas and HTML. πππ
-
Recommend Topics
-
javascript
JavaScript (JS) is a lightweight interpreted programming language with first-class functions.
-
web
Some thing interesting about web. New door for the world.
-
server
A server is a program made to process requests and deliver data to clients.
-
Machine learning
Machine learning is a way of modeling and interpreting data that allows a piece of software to respond intelligently.
-
Visualization
Some thing interesting about visualization, use data art
-
Game
Some thing interesting about game, make everyone happy.
Recommend Org
-
Facebook
We are working to build community through open source technology. NB: members must have two-factor auth.
-
Microsoft
Open source projects and samples from Microsoft.
-
Google
Google β€οΈ Open Source for everyone.
-
Alibaba
Alibaba Open Source for everyone
-
D3
Data-Driven Documents codes.
-
Tencent
China tencent open source team.
from seq2science.