@@ -144,7 +144,7 @@ Here's a well-structured **README.md** example with the series of steps you prov
Follow these steps to initialize and manage a phenotype using `acmc`. In this example, we use a source concept code list for the Concept Set `Abdominal Pain` created from [ClinicalCodes.org](ClinicalCodes.org). The source concept codes are is read2. We genereate versioned phenotypes for read2 and then translate to snomed with a another version.
### **1. Initialize the Phenotype in the Workspace**
1.**Initialize a phenotype in the workspace**
Use the followijng acmc command to initialize the phenotype in a local Git repository:
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@@ -152,23 +152,23 @@ Use the followijng acmc command to initialize the phenotype in a local Git repos
acmc phen init
```
### **2. Copy Example Medical Code Lists to the Phenotype Code Directory**
2.**Copy example medical code lists to the phenotype codes directory**
Copy medical code lists to the phenotype code directory:
From the command prompt, copy medical code lists `/examples/codes`to the phenotype code directory:
```bash
cp-r ./examples/codes/* ./workspace/phen/codes
```
### **3. Copy the Example Phenotype Configuration Files**
3.**Copy the example phenotype configuration file to the phenotype directory**
Copy example phenotype configuration files (`.json`) to the phenotype directory:
From the command prompt, copy example phenotype configuration files `/examples/config.json` to the phenotype directory:
```bash
cp-r ./examples/config.json ./workspace/phen
```
### **4. Validate the Phenotype Configuration**
4.**Validate the phenotype configuration**
Use the followijng acmc command to validate the phenotype configuration to ensure it's correct:
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@@ -176,7 +176,7 @@ Use the followijng acmc command to validate the phenotype configuration to ensur
acmc phen validate
```
### **5. Generate Phenotype in Read2 Format**
5.**Generate phenotype in read2 code format**
Use the followijng acmc command to generate the phenotype in `read2` format:
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...
@@ -184,39 +184,41 @@ Use the followijng acmc command to generate the phenotype in `read2` format:
acmc phen map -t read2
```
### **6. Publish the Phenotype at an Initial Version**
6.**Publish phenotype at an initial version**
Use the followijng acmc command to publish the phenotype at an initial version:
Use the following `acmc` command to publish the phenotype at an initial version:
```bash
acmc phen publish
```
### **7. Generate Phenotype in SNOMED Format**
7.**Generate phenotype in SNOWMED code format**
Generate the phenotype in `SNOMED` format:
Generate the phenotype in `snomed` format:
```bash
acmc phen map -t snomed
```
### **8. Get a Copy of the Previous Version in the Repo**
8.**Get a copy of the previous version from the repo**
Retrieve a copy of the previous version (`v1.0.3`) from the repository:
Use the following `acmc` command to retrieve a copy of the previous version (`v1.0.3`) from the repository:
```bash
acmc phen copy -v v1.0.3
```
### **9. Compare the Previous Version `v1.0.3` with the Latest Version**
Compare the previous version (`v1.0.3`) with the latest version in the repository:
9.**Compare the previous version `v1.0.3` with the latest version**
Use the following `acmc` command to compare the previous version (`v1.0.3`) with the latest version in the repository:
```bash
python acmc.py phen diff -old ./workspace/v1.0.3/
```
### **10. Publish the Phenotype at the Next Version**
10.**Publish the phenotype at the next version**
Use the followijng acmc command to publish the phenotype at the next version:
Use the following `acmc` command to publish the phenotype at the next version: