Skip to content

Latest commit

 

History

History
25 lines (19 loc) · 2.05 KB

users_guide.md

File metadata and controls

25 lines (19 loc) · 2.05 KB

logistic regression model to predict SNV risk level and user selection

逻辑回归模型预测SNV的致病性和用户选择

7/26/2019
Xinglin (Jason) Jia
贾兴霖

Two Logistic regression models, first model classifies SNV to 2 levels: non-pathogenic, and pathogenic using variables "Clinvar score", "HGMD", "SIFT", "polyphen2", "pheno_score", "count", "REVEL","M-CAP”,”ExonicFunc_refGene";
两个逻辑回归模型,第一个模型把SNV分类为两类,非致病和致病;
the second model use predictions from first model to predict if user will select. This model classifies predicted pathogenic data to 2 levels: selected, not selected.
第二个模型使用第一个模型的结果预测用户是否选择该SNV,该模型把SNV分类成两类,选择与不选择

Users are recommended to select from the first result, using the prediction as a reference.
推荐用户通过第一个模型的预测选择,将第二个模型的结果作为参考量

users's guide 使用方法

Put LR_model_all.py, c_or_not_lr_model.sav, c_or_not_lr_scalar.sav, p_or_not_lr_model.sav, p_or_not_lr_scalar.sav in a same folder, open LR_model_all.py using python3,
将 LR_model_all.py, c_or_not_lr_model.sav, c_or_not_lr_scalar.sav, p_or_not_lr_model.sav, p_or_not_lr_scalar.sav放在同一个文件夹,使用python 3打开LR_model_all.py
all procedures are put in one function LR_model_all, input a table, output 6 columns:
数据处理流程和调出模型等流程都被做成了一个方程LR_model_all,输入为一张表格,输出六列数值:
1st column is chromosome and location, 2nd column is HGVS information, third column p_pred is prediction of pathogenic or not, 4th column p_prob is the probability of the third column being 0, 5th column c_pred is prediction of user select or not, 6th column c_prob is the probability of the sixth column being 0
第一列染色体位置,第二列HGVS,第三列p_pred预测是否致病,第四列p_prob为p_pred为0的概率,第五列c_pred预测用户是否选择,第六列c_prob为c_pred为0的概率