It is quite common to find ML-based applications embedded with real-time patient data available from different healthcare systems in multiple countries, thereby increasing the efficacy of new treatment options which were unavailable before. This data set is all about predicting whether the cancer cells are benign or malignant.
Information about attributes:
There are total 10 attributes(int)- Sample code number: id number Clump Thickness: 1 - 10 Uniformity of Cell Size: 1 - 10 Uniformity of Cell Shape: 1 - 10 Marginal Adhesion: 1 - 10 Single Epithelial Cell Size: 1 - 10 Bare Nuclei: 1 - 10 Bland Chromatin: 1 - 10 Normal Nucleoli: 1 - 10 Mitoses: 1 - 10 Predicted class: 2 for benign and 4 for malignant
This data set(Original Wisconsin Breast Cancer Database) is taken from UCI Machine Learning Repository.
This is the first ever data set I am sharing in Kaggle. It would be a great pleasure if you find this data set useful to develop your own model. Hope this simple data set will help beginners to develop their own models for classification and learn how to make their model even better.
Source:
Creators:
Dr. William H. Wolberg, General Surgery Dept. University of Wisconsin, Clinical Sciences Center Madison, WI 53792 wolberg '@' eagle.surgery.wisc.edu
W. Nick Street, Computer Sciences Dept. University of Wisconsin, 1210 West Dayton St., Madison, WI 53706 street '@' cs.wisc.edu 608-262-6619
Olvi L. Mangasarian, Computer Sciences Dept. University of Wisconsin, 1210 West Dayton St., Madison, WI 53706 olvi '@' cs.wisc.edu
Donor:
Nick Street
Data Set Information:
Features are computed from a digitized image of a fine needle aspirate (FNA) of a breast mass. They describe characteristics of the cell nuclei present in the image. A few of the images can be found at [Web Link]
Separating plane described above was obtained using Multisurface Method-Tree (MSM-T) [K. P. Bennett, "Decision Tree Construction Via Linear Programming." Proceedings of the 4th Midwest Artificial Intelligence and Cognitive Science Society, pp. 97-101, 1992], a classification method which uses linear programming to construct a decision tree. Relevant features were selected using an exhaustive search in the space of 1-4 features and 1-3 separating planes.
The actual linear program used to obtain the separating plane in the 3-dimensional space is that described in: [K. P. Bennett and O. L. Mangasarian: "Robust Linear Programming Discrimination of Two Linearly Inseparable Sets", Optimization Methods and Software 1, 1992, 23-34].
This database is also available through the UW CS ftp server: ftp ftp.cs.wisc.edu cd math-prog/cpo-dataset/machine-learn/WDBC/
Attribute Information:
1) ID number 2) Diagnosis (M = malignant, B = benign) 3-32)
Ten real-valued features are computed for each cell nucleus:
a) radius (mean of distances from center to points on the perimeter) b) texture (standard deviation of gray-scale values) c) perimeter d) area e) smoothness (local variation in radius lengths) f) compactness (perimeter^2 / area - 1.0) g) concavity (severity of concave portions of the contour) h) concave points (number of concave portions of the contour) i) symmetry j) fractal dimension ("coastline approximation" - 1)
For more information about **Relevant Papers and Papers That Cite This Data Set, please go here
Citation Policy:
If you publish material based on databases obtained from this repository, then, in your acknowledgements, please note the assistance you received by using this repository. This will help others to obtain the same data sets and replicate your experiments. We suggest the following pseudo-APA reference format for referring to this repository:
Lichman, M. (2013). UCI Machine Learning Repository [http://archive.ics.uci.edu/ml]. Irvine, CA: University of California, School of Information and Computer Science.
Here is a BiBTeX citation as well:
@misc{Lichman:2013 ,
author = "M. Lichman",
year = "2013",
title = "{UCI} Machine Learning Repository",
url = "http://archive.ics.uci.edu/ml",
institution = "University of California, Irvine, School of Information and Computer Sciences" }
A few UCI data sets have additional citation requests. These requests can be found on the bottom of each data set's web page.
Source: UCI Machine Learning Repository
This data was donated by researchers of the University of Wisconsin and includes the measurements from digitized images of fine-needle aspirate of a breast mass.
You can find the dataset at https://github.com/dataspelunking/MLwR/blob/master/Machine%20Learning%20with%20R%20(2nd%20Ed.)/Chapter%2003/wisc_bc_data.csv.
The breast cancer data includes 569 examples of cancer biopsies, each with 32 features. One feature is an identification number, another is the cancer diagnosis and 30 are numeric-valued laboratory measurements. The diagnosis is coded as "M" to indicate malignant or "B" to indicate benign.
The other 30 numeric measurements comprise the mean, standard error and worst (i.e. largest) value for 10 different characteristics of the digitized cell nuclei, which are as follows:-
Creator:
Dr. WIlliam H. Wolberg (physician)
University of Wisconsin Hospitals
Madison, Wisconsin, USA
Donor:
Olvi Mangasarian (mangasarian '@' cs.wisc.edu)
Received by David W. Aha (aha '@' cs.jhu.edu)
Samples arrive periodically as Dr. Wolberg reports his clinical cases. The database therefore reflects this chronological grouping of the data. This grouping information appears immediately below, having been removed from the data itself:
Group 1: 367 instances (January 1989)
Group 2: 70 instances (October 1989)
Group 3: 31 instances (February 1990)
Group 4: 17 instances (April 1990)
Group 5: 48 instances (August 1990)
Group 6: 49 instances (Updated January 1991)
Group 7: 31 instances (June 1991)
Total: 699 points (as of the donated datbase on 15 July 1992)
Note that the results summarized above in Past Usage refer to a dataset of size 369, while Group 1 has only 367 instances. This is because it originally contained 369 instances; 2 were removed. The following statements summarizes changes to the original Group 1's set of data:
Wolberg, W.H., & Mangasarian, O.L. (1990). Multisurface method of pattern separation for medical diagnosis applied to breast cytology. In Proceedings of the National Academy of Sciences, 87, 9193*9196.
Zhang, J. (1992). Selecting typical instances in instance-based learning. In Proceedings of the Ninth International Machine Learning Conference (pp. 470*479). Aberdeen, Scotland: Morgan Kaufmann.
This breast cancer databases was obtained from the University of Wisconsin Hospitals, Madison from Dr. William H. Wolberg. If you publish results when using this database, then please include this information in your acknowledgements. Also, please cite one or more of:1. O. L. Mangasarian and W. H. Wolberg: "Cancer diagnosis via linear programming", SIAM News, Volume 23, Number 5, September 1990, pp 1 & 18.2. William H. Wolberg and O.L. Mangasarian: "Multisurface method of pattern separation for medical diagnosis applied to breast cytology", Proceedings of the National Academy of Sciences, U.S.A., Volume 87, December 1990, pp 9193-9196.3. O. L. Mangasarian, R. Setiono, and W.H. Wolberg: "Pattern recognition via linear programming: Theory and application to medical diagnosis", in: "Large-scale numerical optimization", Thomas F. Coleman and Yuying Li, editors, SIAM Publications, Philadelphia 1990, pp 22-30.4. K. P. Bennett & O. L. Mangasarian: "Robust linear programming discrimination of two linearly inseparable sets", Optimization Methods and Software 1, 1992, 23-34 (Gordon & Breach Science
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Analysis of ‘Breast Cancer Wisconsin (Diagnostic) Data Set’ provided by Analyst-2 (analyst-2.ai), based on source dataset retrieved from https://www.kaggle.com/uciml/breast-cancer-wisconsin-data on 28 January 2022.
--- Dataset description provided by original source is as follows ---
Features are computed from a digitized image of a fine needle aspirate (FNA) of a breast mass. They describe characteristics of the cell nuclei present in the image. n the 3-dimensional space is that described in: [K. P. Bennett and O. L. Mangasarian: "Robust Linear Programming Discrimination of Two Linearly Inseparable Sets", Optimization Methods and Software 1, 1992, 23-34].
This database is also available through the UW CS ftp server: ftp ftp.cs.wisc.edu cd math-prog/cpo-dataset/machine-learn/WDBC/
Also can be found on UCI Machine Learning Repository: https://archive.ics.uci.edu/ml/datasets/Breast+Cancer+Wisconsin+%28Diagnostic%29
Attribute Information:
1) ID number 2) Diagnosis (M = malignant, B = benign) 3-32)
Ten real-valued features are computed for each cell nucleus:
a) radius (mean of distances from center to points on the perimeter) b) texture (standard deviation of gray-scale values) c) perimeter d) area e) smoothness (local variation in radius lengths) f) compactness (perimeter^2 / area - 1.0) g) concavity (severity of concave portions of the contour) h) concave points (number of concave portions of the contour) i) symmetry j) fractal dimension ("coastline approximation" - 1)
The mean, standard error and "worst" or largest (mean of the three largest values) of these features were computed for each image, resulting in 30 features. For instance, field 3 is Mean Radius, field 13 is Radius SE, field 23 is Worst Radius.
All feature values are recoded with four significant digits.
Missing attribute values: none
Class distribution: 357 benign, 212 malignant
--- Original source retains full ownership of the source dataset ---
CC0 1.0 Universal Public Domain Dedicationhttps://creativecommons.org/publicdomain/zero/1.0/
Les informations sur la licence ont été dérivées automatiquement
This dataset was created by Thulani Tembo
Released under CC0: Public Domain
Apache License, v2.0https://www.apache.org/licenses/LICENSE-2.0
Les informations sur la licence ont été dérivées automatiquement
Diagnostic Wisconsin Breast Cancer Database.Dataset Characteristics Features are computed from a digitized image of a fine needle aspirate (FNA) of a breast mass. They describe characteristics of the cell nuclei present in the image. A few of the images can be found at http://www.cs.wisc.edu/~street/images/
Separating plane described above was obtained using Multisurface Method-Tree (MSM-T) [K. P. Bennett, "Decision Tree Construction Via Linear Programming." Proceedings of the 4th Midwest Artificial Intelligence and Cognitive Science Society, pp. 97-101, 1992], a classification method which uses linear programming to construct a decision tree. Relevant features were selected using an exhaustive search in the space of 1-4 features and 1-3 separating planes.
The actual linear program used to obtain the separating plane in the 3-dimensional space is that described in: [K. P. Bennett and O. L. Mangasarian: "Robust Linear Programming Discrimination of Two Linearly Inseparable Sets", Optimization Methods and Software 1, 1992, 23-34].
This database is also available through the UW CS ftp server: ftp ftp.cs.wisc.edu cd math-prog/cpo-dataset/machine-learn/WDBC/
Attribution 4.0 (CC BY 4.0)https://creativecommons.org/licenses/by/4.0/
Les informations sur la licence ont été dérivées automatiquement
Analysis of ‘Wisconsin Diagnostic Breast Cancer (WDBC)’ provided by Analyst-2 (analyst-2.ai), based on source dataset retrieved from https://www.kaggle.com/mohaiminul101/wisconsin-diagnostic-breast-cancer-wdbc on 30 September 2021.
--- Dataset description provided by original source is as follows ---
Breast cancer is a disease in which cells in the breast grow out of control. There are different kinds of breast cancer. The kind of breast cancer depends on which cells in the breast turn into cancer. Wisconsin Diagnostic Breast Cancer (WDBC) dataset obtained by the university of Wisconsin Hospital is used to classify tumors as benign or malignant.
Attribute Information:
1) ID number 2) Diagnosis (M = malignant, B = benign) 3-32)
Ten real-valued features are computed for each cell nucleus:
a) radius (mean of distances from center to points on the perimeter) b) texture (standard deviation of gray-scale values) c) perimeter d) area e) smoothness (local variation in radius lengths) f) compactness (perimeter^2 / area - 1.0) g) concavity (severity of concave portions of the contour) h) concave points (number of concave portions of the contour) i) symmetry j) fractal dimension ("coastline approximation" - 1)
The mean, standard error and "worst" or largest (mean of the three largest values) of these features were computed for each image, resulting in 30 features. For instance, field 3 is Mean Radius, field 13 is Radius SE, field 23 is Worst Radius.
All feature values are recoded with four significant digits.
Missing attribute values: none
Class distribution: 357 benign, 212 malignant
Creator: Dr. WIlliam H. Wolberg (physician) University of Wisconsin Hospitals Madison, Wisconsin, USA
This database is also available through the UW CS ftp server: ftp ftp.cs.wisc.edu cd math-prog/cpo-dataset/machine-learn/WDBC/
Also can be found on UCI Machine Learning Repository: https://archive.ics.uci.edu/ml/datasets/Breast+Cancer+Wisconsin+%28Diagnostic%29
--- Original source retains full ownership of the source dataset ---
Attribution 4.0 (CC BY 4.0)https://creativecommons.org/licenses/by/4.0/
Les informations sur la licence ont été dérivées automatiquement
Analysis of ‘Breast Cancer Wisconsin (Prognostic) Data Set’ provided by Analyst-2 (analyst-2.ai), based on source dataset retrieved from https://www.kaggle.com/sarahvch/breast-cancer-wisconsin-prognostic-data-set on 29 August 2021.
--- Dataset description provided by original source is as follows ---
Data From: UCI Machine Learning Repository http://archive.ics.uci.edu/ml/machine-learning-databases/breast-cancer-wisconsin/wpbc.names
"Each record represents follow-up data for one breast cancer case. These are consecutive patients seen by Dr. Wolberg since 1984, and include only those cases exhibiting invasive breast cancer and no evidence of distant metastases at the time of diagnosis.
The first 30 features are computed from a digitized image of a
fine needle aspirate (FNA) of a breast mass. They describe
characteristics of the cell nuclei present in the image.
A few of the images can be found at
http://www.cs.wisc.edu/~street/images/
The separation described above was obtained using
Multisurface Method-Tree (MSM-T) [K. P. Bennett, "Decision Tree
Construction Via Linear Programming." Proceedings of the 4th
Midwest Artificial Intelligence and Cognitive Science Society,
pp. 97-101, 1992], a classification method which uses linear
programming to construct a decision tree. Relevant features
were selected using an exhaustive search in the space of 1-4
features and 1-3 separating planes.
The actual linear program used to obtain the separating plane
in the 3-dimensional space is that described in:
[K. P. Bennett and O. L. Mangasarian: "Robust Linear
Programming Discrimination of Two Linearly Inseparable Sets",
Optimization Methods and Software 1, 1992, 23-34].
The Recurrence Surface Approximation (RSA) method is a linear
programming model which predicts Time To Recur using both
recurrent and nonrecurrent cases. See references (i) and (ii)
above for details of the RSA method.
This database is also available through the UW CS ftp server:
ftp ftp.cs.wisc.edu
cd math-prog/cpo-dataset/machine-learn/WPBC/
1) ID number 2) Outcome (R = recur, N = nonrecur) 3) Time (recurrence time if field 2 = R, disease-free time if field 2 = N) 4-33) Ten real-valued features are computed for each cell nucleus:
a) radius (mean of distances from center to points on the perimeter)
b) texture (standard deviation of gray-scale values)
c) perimeter
d) area
e) smoothness (local variation in radius lengths)
f) compactness (perimeter^2 / area - 1.0)
g) concavity (severity of concave portions of the contour)
h) concave points (number of concave portions of the contour)
i) symmetry
j) fractal dimension ("coastline approximation" - 1)"
Creators:
Dr. William H. Wolberg, General Surgery Dept., University of
Wisconsin, Clinical Sciences Center, Madison, WI 53792
wolberg@eagle.surgery.wisc.edu
W. Nick Street, Computer Sciences Dept., University of
Wisconsin, 1210 West Dayton St., Madison, WI 53706
street@cs.wisc.edu 608-262-6619
Olvi L. Mangasarian, Computer Sciences Dept., University of
Wisconsin, 1210 West Dayton St., Madison, WI 53706
olvi@cs.wisc.edu
I'm really interested in trying out various machine learning algorithms on some real life science data.
--- Original source retains full ownership of the source dataset ---
Attribution 4.0 (CC BY 4.0)https://creativecommons.org/licenses/by/4.0/
Les informations sur la licence ont été dérivées automatiquement
Analysis of ‘Breast Cancer Wisconsin - benign or malignant’ provided by Analyst-2 (analyst-2.ai), based on source dataset retrieved from https://www.kaggle.com/ninjacoding/breast-cancer-wisconsin-benign-or-malignant on 30 September 2021.
--- Dataset description provided by original source is as follows ---
It is quite common to find ML-based applications embedded with real-time patient data available from different healthcare systems in multiple countries, thereby increasing the efficacy of new treatment options which were unavailable before. This data set is all about predicting whether the cancer cells are benign or malignant.
Information about attributes:
There are total 10 attributes(int)- Sample code number: id number Clump Thickness: 1 - 10 Uniformity of Cell Size: 1 - 10 Uniformity of Cell Shape: 1 - 10 Marginal Adhesion: 1 - 10 Single Epithelial Cell Size: 1 - 10 Bare Nuclei: 1 - 10 Bland Chromatin: 1 - 10 Normal Nucleoli: 1 - 10 Mitoses: 1 - 10 Predicted class: 2 for benign and 4 for malignant
This data set(Original Wisconsin Breast Cancer Database) is taken from UCI Machine Learning Repository.
This is the first ever data set I am sharing in Kaggle. It would be a great pleasure if you find this data set useful to develop your own model. Hope this simple data set will help beginners to develop their own models for classification and learn how to make their model even better.
--- Original source retains full ownership of the source dataset ---
Diagnostic Wisconsin Breast Cancer Database
Prognostic Wisconsin Breast Cancer Database
CC0 1.0 Universal Public Domain Dedicationhttps://creativecommons.org/publicdomain/zero/1.0/
Les informations sur la licence ont été dérivées automatiquement
Context Cytology features of breast cancer biopsy. It can be used to predict breast cancer from cytology features. The data was obtained from https://archive.ics.uci.edu/ml/datasets/Breast+Cancer+Wisconsin+(Original) Data description can be found at https://archive.ics.uci.edu/ml/machine-learning-databases/breast-cancer-wisconsin/breast-cancer-wisconsin.names Content Data contains cytology features of breast cancer biopsies - clump thickness, uniformity of cell size, uniformity of cell shape, marginal adhesion, single epithelial cell size, bare nuclei, bland chromatin, normal nuceloli, mitosis. The class variable denotes whether it was cancer or not. Cancer = 1 and not cancer = 0 Attribute Information:
Sample code number: id number Clump Thickness: 1 - 10 Uniformity of Cell Size: 1 - 10 Uniformity of Cell Shape: 1 - 10 Marginal Adhesion: 1 - 10 Single Epithelial Cell Size: 1 - 10 Bare Nuclei: 1 - 10 Bland Chromatin: 1 - 10 Normal Nucleoli: 1 - 10 Mitoses: 1 - 10 Class: (0 for benign, 1 for malignant)
Acknowledgements Data obtained from : UCI machine learning repository Dua, D. and Karra Taniskidou, E. (2017). UCI Machine Learning Repository [http://archive.ics.uci.edu/ml]. Irvine, CA: University of California, School of Information and Computer Science. Picture courtesy: Photo by Pablo Heimplatz on Unsplash
UCI Breast Cancer Raw Dataset is a breast cancer dataset that contains three sets of breast cancer cytopathology image data. Features are calculated from digitized images of fine needle aspiration (FNA) of breast masses. They describe the image The characteristics of the nuclei appearing in . The original UCI Breast Cancer dataset was published in 1995 by Dr. William H. Wolberg, General Surgery Dept. W. Nick Street, Computer Sciences Dept. Olvi L. Mangasarian, Computer Sciences Dept. Related papers are Breast cancer diagnosis and prognosis via linear programming etc.
Diagnostic Wisconsin Breast Cancer Database
What's inside is more than just rows and columns. Make it easy for others to get started by describing how you acquired the data and what time period it represents, too.
Features are computed from a digitized image of a fine needle aspirate (FNA) of a breast mass. They describe characteristics of the cell nuclei present in the image. n the 3-dimensional space is that described in: [K. P. Bennett and O. L. Mangasarian: "Robust Linear Programming Discrimination of Two Linearly Inseparable Sets", Optimization Methods and Software 1, 1992, 23-34].
This database is also available through the UW CS ftp server: ftp ftp.cs.wisc.edu cd math-prog/cpo-dataset/machine-learn/WDBC/
Also can be found on UCI Machine Learning Repository: https://archive.ics.uci.edu/ml/datasets/Breast+Cancer+Wisconsin+%28Diagnostic%29
Attribute Information:
1) ID number 2) Diagnosis (M = malignant, B = benign) 3-32)
Ten real-valued features are computed for each cell nucleus:
a) radius (mean of distances from center to points on the perimeter) b) texture (standard deviation of gray-scale values) c) perimeter d) area e) smoothness (local variation in radius lengths) f) compactness (perimeter^2 / area - 1.0) g) concavity (severity of concave portions of the contour) h) concave points (number of concave portions of the contour) i) symmetry j) fractal dimension ("coastline approximation" - 1)
The mean, standard error and "worst" or largest (mean of the three largest values) of these features were computed for each image, resulting in 30 features. For instance, field 3 is Mean Radius, field 13 is Radius SE, field 23 is Worst Radius.
All feature values are recoded with four significant digits.
Missing attribute values: none
Class distribution: 357 benign, 212 malignant
Using Machine Learning and AI to contribute in cancer treatment
CC0 1.0 Universal Public Domain Dedicationhttps://creativecommons.org/publicdomain/zero/1.0/
Les informations sur la licence ont été dérivées automatiquement
Original data from: https://archive.ics.uci.edu/ml/datasets/Breast+Cancer+Wisconsin+(Diagnostic). Changes made: - 16 rows with '?' for Bare Nuclei removed, leaving 683 records # Attribute Domain -- ----------------------------------------- 0. Class: (-1 for benign, +1 for malignant) 1. Clump Thickness 1 - 10 2. Uniformity of Cell Size 1 - 10 3. Uniformity of Cell Shape 1 - 10 4. Marginal Adhesion 1 - 10 5. Single Epithelial Cell Size 1 - 10 6. Bare Nuclei 1 - 10 7. Bland Chromatin 1 - 10 8. Normal Nucleoli 1 - 10 9. Mitoses 1 - 10
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Features are computed from a digitized image of a fine needle aspirate (FNA) of a breast mass. They describe characteristics of the cell nuclei present in the image.n the 3-dimensional space is that described in: [K. P. Bennett and O. L. Mangasarian: "Robust Linear Programming Discrimination of Two Linearly Inseparable Sets", Optimization Methods and Software 1, 1992, 23-34].This database is also available through the UW CS ftp server:ftp ftp.cs.wisc.educd math-prog/cpo-dataset/machine-learn/WDBC/Also can be found on UCI Machine Learning Repository: https://archive.ics.uci.edu/ml/datasets/Breast+Cancer+Wisconsin+(Diagnostic)
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The book Cancer is a bitch, or, I'd rather be having a midlife crisis is about Breast-Cancer-Patients-Wisconsin-Biography and was written by Gail Konop Baker. It was published in 2008.
Creators:
Matjaz Zwitter & Milan Soklic (physicians)
Institute of Oncology University Medical Center
Ljubljana, Yugoslavia
Donors:
Ming Tan and Jeff Schlimmer (Jeffrey.Schlimmer '@' a.gp.cs.cmu.edu)
This is one of three domains provided by the Oncology Institute that has repeatedly appeared in the machine learning literature. (See also lymphography and primary-tumor.)
This data set includes 201 instances of one class and 85 instances of another class. The instances are described by 9 attributes, some of which are linear and some are nominal.
Michalski,R.S., Mozetic,I., Hong,J., & Lavrac,N. (1986). The Multi-Purpose Incremental Learning System AQ15 and its Testing Application to Three Medical Domains. In Proceedings of the Fifth National Conference on Artificial Intelligence, 1041-1045, Philadelphia, PA: Morgan Kaufmann.
Clark,P. & Niblett,T. (1987). Induction in Noisy Domains. In Progress in Machine Learning (from the Proceedings of the 2nd European Working Session on Learning), 11-30, Bled, Yugoslavia: Sigma Press.
Tan, M., & Eshelman, L. (1988). Using weighted networks to represent classification knowledge in noisy domains. Proceedings of the Fifth International Conference on Machine Learning, 121-134, Ann Arbor, MI.
Cestnik,G., Konenenko,I, & Bratko,I. (1987). Assistant-86: A Knowledge-Elicitation Tool for Sophisticated Users. In I.Bratko & N.Lavrac (Eds.) Progress in Machine Learning, 31-45, Sigma Press.
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Breast Cancer Data-set is also used for collecting the data for constructing the patient record files. The numbers of attributes are Id number, cell size, and shape, class attributes such as a benign tumor or malicious tumor andso on. THIS DATASET IS ARCHIVED AT DANS/EASY, BUT NOT ACCESSIBLE HERE. TO VIEW A LIST OF FILES AND ACCESS THE FILES IN THIS DATASET CLICK ON THE DOI-LINK ABOVE
It is quite common to find ML-based applications embedded with real-time patient data available from different healthcare systems in multiple countries, thereby increasing the efficacy of new treatment options which were unavailable before. This data set is all about predicting whether the cancer cells are benign or malignant.
Information about attributes:
There are total 10 attributes(int)- Sample code number: id number Clump Thickness: 1 - 10 Uniformity of Cell Size: 1 - 10 Uniformity of Cell Shape: 1 - 10 Marginal Adhesion: 1 - 10 Single Epithelial Cell Size: 1 - 10 Bare Nuclei: 1 - 10 Bland Chromatin: 1 - 10 Normal Nucleoli: 1 - 10 Mitoses: 1 - 10 Predicted class: 2 for benign and 4 for malignant
This data set(Original Wisconsin Breast Cancer Database) is taken from UCI Machine Learning Repository.
This is the first ever data set I am sharing in Kaggle. It would be a great pleasure if you find this data set useful to develop your own model. Hope this simple data set will help beginners to develop their own models for classification and learn how to make their model even better.