osf.io | Facilitating Open Science | REST library
kandi X-RAY | osf.io Summary
kandi X-RAY | osf.io Summary
Facilitating Open Science
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Top functions reviewed by kandi - BETA
- Create a url map .
- Handle a registration row .
- Merges another user into this project .
- Render a project .
- Create migrations for the given nodes .
- Return all registries .
- Generate a citation for a given document .
- Prepare for registration bulk creation
- Validate a user .
- Return the auth response
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Trending Discussions on osf.io
QUESTION
This is an extension of a question I asked yesterday. I have looked all over StackOverflow and have not found an instance of this specific NameError:
...ANSWER
Answered 2022-Jan-06 at 06:30I think it's due to you used expand
function in a wrong way, expand
only accepts two positional arguments, where the first one is pattern and the second one is function (optional). If you want to supply multiple patterns you should wrap these patterns in list.
After some studying on source code of snakemake, it turns out expand
function doesn't check if user provides < 3 positional arguments, there is a variable combinator
in if-else
that would only be created when there are 1 or 2 positional arguments, the massive amount of positional arguments you provide skip this part and lead to the error when it tries to use combinator
later.
Source code: https://snakemake.readthedocs.io/en/v6.5.4/_modules/snakemake/io.html
QUESTION
I am trying to do QC on RNAseq data that is tarballed. I am using Snakemake as a workflow manager and am aware that Snakemake does not like one-to-many rules. I defining a checkpoint would fix the problem but when I run the script I get this this error message with rule fastqc.
...ANSWER
Answered 2022-Jan-05 at 06:18First, glob_wildcards(INPUTDIR + "{basenames}_R1.fastq.gz")
returns a Wildcards object that contains the key:value pair for each wildcard. If you want to get the basenames, it should be glob_wildcards(INPUTDIR + "{basenames}_R1.fastq.gz").basenames
Second, I assume all fastq.gz files are generated by decompress_h1n1
checkpoint, since you already include the fastqc output in aggregate_decompress_h1n1
function. You shouldn't include those outputs again in rule all
, it leads to snakemake try to do fastqc before checkpoint got executed.
Third, you should also put your trim_qc
outputs in the aggregate_decompress_h1n1
function, basically it's the same issue as fastqc, probably the same for salmon
related rules too.
There might be a potential issue, I noticed you use wrapper for fastqc, I remember that official fastqc wrapper requires the output must have html
and zip
, while you have a raw
prefix. But I didn't see a 0.80.3
release in official document, not sure if you are using some other repository to access wrapper
QUESTION
I have this dataset
...ANSWER
Answered 2021-Dec-01 at 18:10The wrong link was used in the question. The correct link can be found by going to https://osf.io/nkdw5/, then clicking on filter_raw.csv
in the Data
section, and then copying the link from the download button (upper right of page).
Here the solution that has worked better.
QUESTION
I'm trying creating a table on the following dataset which I'm reporting here the very first fifty observations. Here following it is reported the dataset I'm working on.
There are some typos for age and gnder variable that I susggest to fix as follows:
...ANSWER
Answered 2021-Sep-14 at 21:34I would like to help you. However, there are the following problems with the data you provide:
- The variable
COND
is missing - Only one unique value of the
TASK
variable (theCreateTableOne
function does not accept variables with one unique value). - Only one unique value for the variable
age
. - The variable
ID
is repeated several times.
However, even without changing your data, you can see what your problem is. If you have data in this form, you cannot use CreateTableOne
! This is because it counts every occurrence of the value m
and every occurrence of the value k
. And since you have multiple entries for one person, the CreateTableOne
function will count each occurrence separately.
Please take a look at the solution I have proposed here How to describe unique values of grouped observations for several vars?.
Update 1
OKAY. Let's try to face your data. You have 54 patients with different IDs.
QUESTION
I found a nice function on OSF, which I would like to apply to my own data: https://osf.io/huy8b/
However, if I try to use the lapply function, I get an error. My code and sample data (my own dataset is much bigger) are here.
...ANSWER
Answered 2021-Mar-29 at 13:49These are not suitable places to use lapply
. The functions just take the data frames as inputs, so you can just use the functions. For example:
QUESTION
I'm looking for an efficient function to automatically produce betas for every possible multiple regression model given a dependent variable and set of predictors as a DataFrame in python.
For example, given this set of data:
https://i.stack.imgur.com/YuPuv.jpg
The dependent variable is 'Cases per Capita' and the columns following are the predictor variables.
In a simpler example:
...ANSWER
Answered 2020-Apr-08 at 22:02I am not aware of any package that already does this. But you can create all those combinations (2^n-1), where n is the number of columns in X (independent variables), and fit a linear regression model for each combination and then get coefficients/betas for each model.
Here is how I would do it, hope this helps
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