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Full spec to be confirmed once data mapping/processing complete
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Preliminary notes:
- Basic data table implementation
- Data table to be displayed under the `Pathways and systems biology` tab
- Cells within data table may contain link to Project Score website
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- [x] announcement text
Unexpected insertion of carrier DNA during CRISPR–Cas9, and "unknowns" remain "unknown"
image ![spotlight](https://user-images.githubusercontent.com/7359272/56200239-4…
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Hello
I am trying to run the CRISPRessoPooled command on the pooled deep sequencing data.
i run my script several times as per suggestion, but got an error "ERROR: Flash failed to run, please check…
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Environment: CentOS6.5, Python 2.7.11, CRISPResso installed from source (master.zip downloaded from github), needle, flash and trimmomatic are in the CRISPResso dependencies dir.
Data was downloaded…
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Dear Luca Pinello
I am using CRISPRessoPooled.py script to analyzed the paired ends reads data by Illumina.
the read length is 150 bp.
the amplicon size is 180bp long.
below is the command that I…
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We have not yet determined what it means when an arrow has multiple sources or multiple sinks.
The fundamental ambiguity in drawings at present is that this is currently used to mean two things:
1. …
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Update the following URL to point to the GitHub repository of
the package you wish to submit to _Bioconductor_
- Repository: https://github.com/UCLouvain-CBIO/depmap
Confirm the following by ed…
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Hi,
I am trying to install CRISPResso on my computer, but am having trouble using FLASH. Here's the output I get when I try to run the example files:
CRISPResso -r1 reads1.fastq -r2 reads2.fast…
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potentially related to datacite/bolognese#36
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