Run name:
Email (optional):

Sequence/reads file: FASTQ (compressed or uncompressed)
Max. 2000 MB Download example

Or file URL:

Paired-end reads file (optional): FASTQ (compressed or uncompressed)
Max. 2000 MB

Or file URL:

Data type: Gene Panel   (Exome-Seq and RNA-Seq will be included soon)

Cancer type: Highlights the genetic variants found in the genes related with a particular tumor type.

Detect indels and translocations: This option is not available at the moment.

AmpliCANCER has been developed for research purposes and it is not intended for human diagnosis.

I develope this tool in my free time without any academic/commercial support, I will be grateful if you want to contribute:


Your use of any of these tools is at your own risk. We do not give any representation or warranty nor assume any liability or responsibility for the data nor the results posted (whether as to their accuracy, completeness, quality or otherwise). Access to these data is available free of charge for ordinary use in the course of research. By visiting the site, you accept our use of cookies and you accept that your data and results will be stored in our server.