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Table 2 REST API arguments and parameters supported by BRCA-Pathway

From: BRCA-Pathway: a structural integration and visualization system of TCGA breast cancer data on KEGG pathways

arg1

arg2

arg3

Parameters

Description

landscape

-

-

type=[JSON | LIST]

 
   

fields=[KEGGPathway_update

 
   

| KEGGPathways

 
   

| Pathway_Pathway_Membership

KEGG pathways, TCGA-

   

| TCGAGenes

BRCA data status

   

| TCGA_BRCA_Patients

 
   

| TCGA_BRCA_update

 
   

| TFTG_relation | driver_genes]

 

search

-

-

keyword

 
   

type=[ JSON | LIST ]

Get search result by

   

fields=[ keyword

keyword.

   

| gene_labels

Gene or pathway names

   

| rate

with input_type.

   

| pathID | pathname ]

 

genes

(pathIDs,

-

type=[ JSON | LIST ]

 
 

sep=“+”)

count

fields=[ pathID

Retrieve pathways

   

| gene_symbol

information.

   

| pathname

related_pathways operation

   

| geneID

supported.

   

| count** ]

 
   

**given only arg3 related_pathways

 

pathways

(pathIDs,

-

type=[ JSON | LIST ]

 
 

sep=“+”)

related_pathways

fields=[ pathID | pathname

Retrieve pathways

   

| category_level2_id

information.

   

| description

related_pathways operation

   

| related_pathID**]

supported.

   

**given only arg3 related_pathways

 

TCGA-BRCA

patient_list

-

type=[ JSON | LIST ]

 
 

patient_count

-

** arg2 patient_list

 
 

(pathIDs,

(given pathIDs,)

fields=[patient_barcode]

Retrieve pathways and

 

sep=“+”)

fold_change

 

TCGA-BRCA omics data.

  

mutation

** arg2 patient_count

Gene expression with

  

CNV

fields=[count]

fold_change value,

    

mutation with the number

   

** arg3 fold_change

of patients having

   

fields=[geneID |gene_symbol

mutation, and CNV with

   

| exp_select

GISTIC2 result range from

   

| exp_tumor

-2 to 2.

   

| exp_normal

Each omics result will be

   

| fc_select_tumor | fc_select_normal ]

given by gene level

    

aggregating patients

    

group omics data

   

** arg3 mutation

patient_list,

   

fields=[ geneID | gene_symbol

patient_count operation

   

|count ]

supported.

   

** arg3 CNV

 
   

fields=[geneID | gene_symbol

 
   

| cnv_pos

 
   

| cnv_zero

 
   

| cnv_neg ]

 
   

** And patient_options

 
   

described_above