Comments (6)
Description of the bug
(Just re-pasting my message)
Thank you for this is excellent tool. It has worked fine for me in the past, but I've started getting the message below.
(I can't expect users on the system to have logged in to GitHub.)
Do you know how I can solve the problem? Other nf-core pipelines currently work on my machine.
Steps to reproduce
swingett@cell-bio-xeon:/data1_wingett/Magda/classifier/HipSci_Full_Download$ nextflow run fetcher --input to_download_ERR.txt -bg/data1_wingett/Magda/classifier/HipSci_Full_Download$ N E X T F L O W ~ version 21.04.1
swingett@cell-bio-xeon:
Pulling nextflow-io/fetcher ...
WARN: Cannot read project manifest -- Cause: API rate limit exceeded -- Provide your GitHub user name and password to get a higher rate limit
API rate limit exceeded -- Provide your GitHub user name and password to get a higher rate limit
System
- Hardware:Desktop
- Executor: local
- OS: Ubuntu
- Version Ubuntu 18.04.4 LTS
Nextflow Installation
- Version: version 21.04.1
from fetchngs.
Hi @StevenWingett ! Hope you are well! Long time no speak :)
It looks like you are trying to run a pipeline called fetcher
from the messages above whereas this pipeline is called fetchngs
?
Pulling nextflow-io/fetcher ...
You shouldn't really be hitting any Github API limits with this pipeline as the only download from Github is the pipeline itself and this is only done once when you trigger the run and is cached locally thereafter in ~/.nextflow/assets/nf-core/fetchngs
anyway.
from fetchngs.
Hi,
I am fine thank you and I hope you are well too. Hopefully there will be bioinformatics meet-ups etc. once again before too long.
That is embarrassing :-( That is the second time I have got the name of this pipeline incorrect. Many thanks for your help and it all seems to be working now! Thank you.
Actually, if I may make a suggestion, have you considered at some point adding functionality to rename the downloaded FASTQ files to include sample/species/experiment name, in a similar fashion to Phil's SRA Explorer. Just a suggestion.
Many thanks once again.
All the best,
Steven
from fetchngs.
No worries! 🤞🏽
Yes, we discussed the sample renaming on Slack a few days ago but I am not a big fan of the super-dooper-long names generated by SRAExplorer. Also, the info for this sort of renaming is quite inconsistent in the SRA 😏 As it goes, I have been working on outputting a mappings.tsv
with just some of the pertinent information that can be used to rename the samples downstream or in MultiQC.
from fetchngs.
Hopefully, I will get another release out this week with that included.
from fetchngs.
from fetchngs.
Related Issues (20)
- sra_ids_to_runinfo.py: command not found HOT 3
- TypeError: unsupported operand type(s) for |: 'dict' and 'dict' HOT 1
- error executing process HOT 3
- Add compatibility with sarek samplesheet
- SRAtools download seems to insert paired-end suffix into workdir path HOT 6
- Support .ngc file for dbgap downloads HOT 2
- FEAT: Pass scientific name as input to download the data
- Pipeline fails for large studies HOT 1
- Pipeline crashes if some samples are not available HOT 3
- Use nf-test for input validation
- check out extensions for input files HOT 1
- Add ability to download more than 2 FastQ files via FTP and Aspera HOT 3
- Merge technical replicates (SRR1 + SRR2 -> SRX)
- nf-validation-1.1.3: Operation not supported HOT 20
- `vdb-validate` does not detect file corruption HOT 5
- URGENT: pin nf-validation version HOT 1
- wget host address error HOT 5
- aspera `CONDA_PREFIX` error HOT 1
- Automatic retrieval of input id.csv from test-datasets for test profile HOT 5
- SRA file links deprecated
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from fetchngs.