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Sorry for bringing this up very late, and we may have discussed this during the writing, but now that I'm in the process of submitting metabarcoding data, it becomes obvious that a field specifying se…
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Quoting the README file,
> Set of scripts to annotate Pfam domains and extract NLR plant immune receptors and their architectures as published in Sarris et al BMC Biology 2016: https://bmcbiol.biom…
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#### Summary:
This exists for one subcommand (`--download`), but would be more generally useful (I think).
#### Description:
Currently, I want to see the specific `ANIm` commands that *would* b…
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* DOI 2 cff version: 1.0.0
* Python version: 3.7.3
* Operating System: Debian Buster
### Description
I'm trying to build a Debian package from doi2cff. The usage example
doi2cff init h…
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*Created with consultation with @kaushik-work*
# Use cases
It is a common desire to run an entire script as a CWL step. For example, the user might be converting a `bash` or `make`-based pipelin…
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Hi there,
This is a semi-automated message from a fellow bioinformatician. Through a GitHub search, I found that the following source files make use of BLAST's `-max_target_seqs` parameter:
- [bin/…
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Hello,
I am attempting to retrieve the exons on either side of introns with significant splice QTLs. I am running into an issue where I have to subtract 1 from both the start and stop coordinates i…
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Hi,
Thank you for writing this wonderful program. These figures look really nice.
However, as I have no knowledge of the java program and being a newbie in bioinformatics. I have not been able to …
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I'm just going to leave this here for now so I can remember to do this...
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I am getting this error when I run `multi_to_single_fast5` with Fast5:
`ERROR:ont_fast5_api.conversion_tools.multi_to_single_fast5:Could not convert Multi->Single for file type 'single-read' with p…
akk01 updated
4 years ago