What is a Computer Readable Form (CRF) in the context of sequence listings?
This page is an FAQ based on guidance from the Manual of Patent Examining Procedure. It is provided as guidance, with links to the ground truth sources. This is information only: it is not legal advice.
A Computer Readable Form (CRF) in the context of sequence listings is a standardized electronic format for submitting nucleotide and amino acid sequence information in patent applications. According to MPEP 2421.02, the CRF is an essential component of the sequence listing submission. Key points about CRF include:
- It must be submitted in accordance with the requirements of 37 CFR 1.824.
- The CRF must contain the same sequence information as the written sequence listing.
- It allows for efficient processing and searching of sequence data by the USPTO.
The MPEP states: “Applicants must submit a copy of the sequence listing in computer readable form (CRF) in accordance with the requirements of 37 CFR 1.824.” This requirement ensures that sequence information can be accurately and efficiently processed during patent examination and made available for future reference and searching.