cerebellum | powerful set of tools that help you structure | Frontend Framework library
kandi X-RAY | cerebellum Summary
kandi X-RAY | cerebellum Summary
Cerebellum.js is a powerful set of tools that help you structure your isomorphic apps, just add your preferred view engine. Cerebellum works great in conjunction with React. Cerebellum is designed for single-page apps that need search engine visibility. Same code works on server and client.
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Top functions reviewed by kandi - BETA
- Create a new Client instance .
- Create store options
- Constructs a new Server instance .
- Invoked when the DOM is ready .
- The default handler function
- Create html from a file
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Community Discussions
Trending Discussions on cerebellum
QUESTION
I have one question. Like now i have two files:sampleattributes and genecount.I have filtered sample attributes file and it has a column name sampid and genecount has a column name sampid. I am trying to merge the two files using the common sampid. This is what I have written:
...ANSWER
Answered 2022-Feb-23 at 14:07Looking at youre gene_count
data, it doesn't have a column for the SAMPID, those were imported as row names. We'll convert them to an actual column, replace the "."
with "-"
so they match the braindata format, and then we can join. Your sample data doesn't have any elements in common so I use a full_join
, but you may prefer a left, right, or inner join--I'm not really sure what your use case is.
QUESTION
I need to create a dictionary in order to do some mapping, like so:
...ANSWER
Answered 2022-Feb-12 at 05:34use enumerate()
:
QUESTION
I have two adjacent matrices that represent two brain structures (cerebellum and cortex):
Dataset:
...ANSWER
Answered 2022-Jan-21 at 02:14Here's a way to do what you want:
- First after loading your adjacency matrices to pandas you can convert them to two different graphs with
nx.convert_matrix.from_pandas_adjacency
- You can then join the two graph into a single graph by using
nx.disjoint_union
. The nodes of both graphs are basically concatenated onto a single graph (see more here). - Once you have the full graph, you can randomly draw nodes from the cortex part of the full graph with a 0.01 probability.
- Similarly you can draw the same number of nodes on the cerebellum part of the graph to act as recipients of the connection.
- Finally you can create the edges between the chosen nodes on both sides.
- And you can get your adjacency matrix from the final graph by using
adj_matrix_full=nx.linalg.graphmatrix.adjacency_matrix(full_g,weight=None)
See full code below for more details:
QUESTION
I have two samples from the population of neurons in the brain, each sample consisting of a thousand neuron instances, of categories:
- cerebellum
- cortex
Now I'm extracting multiple metrics for each sample using complex network analysis, for example, neuron degree of connectivity k
, a discreet number n = 0, 1, ...., n, or clustering coefficient C
, a continous value between 0.00000 and 1.00000.
df.sample(3)
(where web is category) in my pandas dataframes:
cortex:
...ANSWER
Answered 2022-Jan-26 at 16:49for the "k" metric:
QUESTION
Based on a dataset extracted from this link: Brain and Cosmic Web samples, I'm trying to do some Complex Network analysis.
The paper The Quantitative Comparison Between the Neuronal Network and the Cosmic Web, claims to have used this dataset, as well as its adjacent matrixes
"Mij
, i.e., a matrix with rows/columns equal to the number of detected nodes, with value Mij
= 1 if the nodes are separated by a distance ≤ llink
, or Mij = 0
otherwise".
I then probed into the matrix, like so:
...ANSWER
Answered 2021-Nov-13 at 02:41This is not really a programming question, but I will try to answer it. The webpage with the data sources states that the adjacent matrix files for brain samples give distances between connected nodes expressed in pixels of the images used to reconstruct the networks. The paper then explains that to get the real adjacency matrix Mij (with 0 and 1 values only) the authors consider as connected nodes where the distance is at most 16 micrometers. I don't see the information on how many pixels in the image corresponds to one micrometer. This would be needed to compute the same matrix Mij that the authors used in their calculations.
Furthermore, the value〈k〉is not the degree centrality or the clustering coefficient (that depend on a node), but rather the average number of connections per node in the network, computed using the matrix Mij. The paper then compares the observed distributions of degree centralities and clustering coefficients in the brain and cosmic networks to the distribution one would see in a random network with the same number of nodes and the same value of〈k〉. The conclusion is that brain and cosmic networks are highly non-random.
Edits:
1. The conversion of 0.32 micrometers per pixel seems to be right. In the files with data on brain samples (both for cortex and cerebellum) the largest value is 50 pixels, which with this conversion corresponds to 16 micrometers. This suggests that the authors of the paper already thresholded the matrices, listing in them only distances not exceeding 16 micrometers. In view of this, to obtain the matrix Mij with 0 and 1 values only, one simply needs to replace all non-zero values with 1. An issue is that using the matrices obtained in this way one gets 〈k〉 = 9.22 for cerebellum and 〈k〉 = 7.13 for cortex, which is somewhat outside the ranges given in the paper. I don't know how to account for this discrepancy.
2. Negative centrality values are due to a mistake (missing parentheses) in the code. It should be:
QUESTION
How can I pass from a code that throws 280 boxplots at once, to a code that separates each variable, and gets me 280 different plots?
All the examples that I have found contain less than 5 variables, making the output easy to handle and to recognize ... but how do you do it with more than 15 variables to plot?
I have a big data set (long format= 77560 observation, 3 variables; wide format= 280 observations, 278 variables). This data set contains clinical data and measurements from 2 groups, patients and controls.
My goal is to boxplot controls against patients, from all the 280 variables, and get the result in different plots (different outcome windows).
I would like to have one code, instead of doing this 280 times.
How can I get the 280 boxplots in a more reasonable output?
Thanks!
The code that I am using is this:
...ANSWER
Answered 2021-Oct-27 at 12:48One option is to use data Standardization. Meaning that you recalculate the values into values between -1 and 1, but keep the relative diferences.
QUESTION
I'm having some issues with assigning my own x and y values for a plot. By default, x and y are combinations of data frame column names.
For example, var_combinations contains:
(('Cerebrum Volume', 'Cerebellum Volume'), ('Cerebrum Volume', 'Cerebellum Surface Area'), ('Cerebellum Volume', 'Cerebellum Surface Area'))
This works great when left alone, see working code below.
...ANSWER
Answered 2021-Oct-09 at 22:14- There are two issues, and they only occur when trying to send a single
tuple
to the function.xy
should be atuple
oftuples
- It should be similar to
(('CerebrumVolume', 'CerebellumVolume '), ('CerebrumVolume', 'CerebellumSurfaceArea'), ('CerebellumVolume ', 'CerebellumSurfaceArea'))
- You are giving it
('Cerebellum Surface Area', 'Cerebrum Volume')
which is not correctly unpacked. xy=(('CerebrumVolume', 'CerebellumVolume '),)
works for sending a singletuple
to the function.
- It should be similar to
- When there is only one set of tuples to unpack,
plt.subplots
creates a singleaxes
instead of an array ofaxes
- Use
squeeze=False
so there will always be an array, even if there is only oneaxes
, and then flatten the array withaxes.flatten()
.
- Use
QUESTION
In my data frame, I have a column named Localisation
. I want to change the data that is stored in it.
Thalamus, External capsule or Lenticulate for 0, Cerebellum or Brain stem for 2 and Frontal, Occipital, Parietal or Temporal for 1
I’m trying to do a For loop for this operation. My for statement doesn’t seem to be right, because I received
...ANSWER
Answered 2021-Jul-06 at 18:23Up front: in general, don't use for
in a %>%
-pipe, it almost never is what you intend.
Since you have the %>%
, I'll infer you're using dplyr
and/or other related packages. Here's one way:
QUESTION
I cannot pass Story #5: "When I click a .nav-link button in the nav element, I am taken to the corresponding section of the landing page." I have all of my href
attributes set to the corresponding id
attributes and when i click on them they take me to the correct section of the page, but I am still failing this test... What am I Doing Wrong???
The code I wrote is below:
...ANSWER
Answered 2021-May-28 at 01:41The error reads
QUESTION
I'm creating a plot that depicts several data points ("region") per individual ("patient"). I'm trying to set the colours denoting the regions to a manual colour blindness-friendly palette:
...ANSWER
Answered 2021-Feb-09 at 09:06You probably need scale_colour_manual
.
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