From 
To
   
 
           
Genome Version  
Select target species
           
Output Type: 
           
 
Target: 
           
Mining Quality:    
Ranking Order:    
Ranking Number:  Ref. Cutoff: 
     
Ranking Number: 

Border of pACT :


Border of pACT :

*Inputs can contain both gene IDs and protein IDs, such as Entrez Gene ID, Gene Symbol, UniProt Entry Name/Accession, Ensembl Gene ID/Transcript ID/Protein ID, RefSeq Accession.
 

Function : Variant analysis workflow

Step 1 : Select VCF File
Step 2 : Check SNP Effect Run Mode
Step 3 : Press Analysis Button
This is the application to analyze VCF file contents generated by SnpEff 3.6/4.0/4.1.
Effect(EFF) and/or Annotation(ANN) records are detected automatically,
then use them with other VCF data record information to find associated additional PDB/UNIPROT information.

VCF file with annotation in VariantGrid style, is acceptable.

Drag & Drop File Here!

SnpEff4.1d

Function : Add dbSNP Annotations

Step 1 : Select VCF File
Step 2 : Select Species or Select Genome Version
Step 3 : Select Genome Version
Step 4 : Select dbSNP Version
Step 5 : Select SNP Match Mode (Exact / Overlap) or Press Analysis Button
Step 6 : Press Analysis Button

Drag & Drop File Here!

           
Genome Version
dbSNP Version

Function : Expression analysis workflow

Step 1 : Select TSV File
Step 2 : Select Gene / Transcript / Protein ID Column & Check Ortholog Gene Options (Only if necessary)
Step 3 : Check Header Record(s) or Press Analysis Button
Step 4 : Press Analysis Button

Drag & Drop File Here!

Function : STest / GSEA / Bayes

Step 1 : Select TSV File
Step 2 : Press Analysis Button

Drag & Drop File Here!

Ready..