Mice Protein Expression
Donated on 8/3/2015
Expression levels of 77 proteins measured in the cerebral cortex of 8 classes of control and Down syndrome mice exposed to context fear conditioning, a task used to assess associative learning.
Dataset Characteristics
Multivariate
Subject Area
Biology
Associated Tasks
Classification, Clustering
Feature Type
Real
# Instances
1080
# Features
80
Dataset Information
Additional Information
The data set consists of the expression levels of 77 proteins/protein modifications that produced detectable signals in the nuclear fraction of cortex. There are 38 control mice and 34 trisomic mice (Down syndrome), for a total of 72 mice. In the experiments, 15 measurements were registered of each protein per sample/mouse. Therefore, for control mice, there are 38x15, or 570 measurements, and for trisomic mice, there are 34x15, or 510 measurements. The dataset contains a total of 1080 measurements per protein. Each measurement can be considered as an independent sample/mouse. The eight classes of mice are described based on features such as genotype, behavior and treatment. According to genotype, mice can be control or trisomic. According to behavior, some mice have been stimulated to learn (context-shock) and others have not (shock-context) and in order to assess the effect of the drug memantine in recovering the ability to learn in trisomic mice, some mice have been injected with the drug and others have not. Classes: c-CS-s: control mice, stimulated to learn, injected with saline (9 mice) c-CS-m: control mice, stimulated to learn, injected with memantine (10 mice) c-SC-s: control mice, not stimulated to learn, injected with saline (9 mice) c-SC-m: control mice, not stimulated to learn, injected with memantine (10 mice) t-CS-s: trisomy mice, stimulated to learn, injected with saline (7 mice) t-CS-m: trisomy mice, stimulated to learn, injected with memantine (9 mice) t-SC-s: trisomy mice, not stimulated to learn, injected with saline (9 mice) t-SC-m: trisomy mice, not stimulated to learn, injected with memantine (9 mice) The aim is to identify subsets of proteins that are discriminant between the classes.
Has Missing Values?
Yes
Introductory Paper
By C. Higuera, K. Gardiner, K. Cios. 2015
Published in PLoS ONE
Variables Table
Variable Name | Role | Type | Description | Units | Missing Values |
---|---|---|---|---|---|
MouseID | ID | Categorical | no | ||
DYRK1A_N | Feature | Continuous | yes | ||
ITSN1_N | Feature | Continuous | no | ||
BDNF_N | Feature | Continuous | yes | ||
NR1_N | Feature | Continuous | no | ||
NR2A_N | Feature | Continuous | yes | ||
pAKT_N | Feature | Continuous | no | ||
pBRAF_N | Feature | Continuous | yes | ||
pCAMKII_N | Feature | Continuous | no | ||
pCREB_N | Feature | Continuous | yes |
0 to 10 of 82
Additional Variable Information
1 Mouse ID 2..78 Values of expression levels of 77 proteins; the names of proteins are followed by “_n†indicating that they were measured in the nuclear fraction. For example: DYRK1A_n 79 Genotype: control (c) or trisomy (t) 80 Treatment type: memantine (m) or saline (s) 81 Behavior: context-shock (CS) or shock-context (SC) 82 Class: c-CS-s, c-CS-m, c-SC-s, c-SC-m, t-CS-s, t-CS-m, t-SC-s, t-SC-m
Dataset Files
File | Size |
---|---|
Data_Cortex_Nuclear.xls | 1.6 MB |
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pip install ucimlrepo
from ucimlrepo import fetch_ucirepo # fetch dataset mice_protein_expression = fetch_ucirepo(id=342) # data (as pandas dataframes) X = mice_protein_expression.data.features y = mice_protein_expression.data.targets # metadata print(mice_protein_expression.metadata) # variable information print(mice_protein_expression.variables)
Higuera, C., Gardiner, K., & Cios, K. (2015). Mice Protein Expression [Dataset]. UCI Machine Learning Repository. https://doi.org/10.24432/C50S3Z.
Creators
Clara Higuera
Katheleen Gardiner
Krzysztof Cios
DOI
License
This dataset is licensed under a Creative Commons Attribution 4.0 International (CC BY 4.0) license.
This allows for the sharing and adaptation of the datasets for any purpose, provided that the appropriate credit is given.