What regulations govern the content of a Sequence Listing XML?

The content of a Sequence Listing XML is governed by specific regulations to ensure consistency and uniformity. According to MPEP 2413, “37 CFR 1.833 defines the content of the ‘Sequence Listing XML.’” This regulation specifies what information must be included in the Sequence Listing XML and how it should be structured. Applicants must adhere to…

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Are provisional applications required to comply with sequence listing requirements?

According to MPEP 2422.07, provisional applications are not required to comply with sequence listing requirements: “Provisional applications filed under 35 U.S.C. 111(b) need not comply with 37 CFR 1.821 through 1.825, however, applicants are encouraged to file a “Sequence Listing” as defined in 37 CFR 1.821(c) for ease of identification of the sequence information contained…

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What are “Sequence Listing” Numeric Identifiers in patent applications?

“Sequence Listing” Numeric Identifiers are specific codes used to organize and present information in the “Sequence Listing” section of patent applications involving nucleotide and/or amino acid sequences. According to MPEP 2424.02, “37 CFR 1.823(a) sets forth the order and presentation of the items of information in the “Sequence Listing”. Each item of information in the…

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How do filing requirements for sequence listings differ between national and international applications?

Filing requirements for sequence listings can vary between national US applications, foreign applications, and international applications. MPEP 2422 highlights some key differences: For international applications filed in paper, the sequence listing part must also be provided in paper. A copy of the sequence listing in ASCII plain text must be filed on read-only optical disc…

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Who can make the required statement regarding the “Sequence Listing” and CRF?

The required statement regarding the information contained in the “Sequence Listing” and the separate Computer Readable Form (CRF) can be made by specific individuals. According to MPEP 2422.06: “Such a statement may be made by a registered practitioner, the applicant, an inventor, or the person who actually compares the sequence data on behalf of the…

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What is the requirement for submitting a separate computer readable form (CRF) of a “Sequence Listing”?

When a separate computer readable form (CRF) of a “Sequence Listing” is submitted in certain patent applications, a statement regarding the information contained in the “Sequence Listing” and the separate CRF is required. Specifically: For applications filed under 35 U.S.C. 111(a) or national stage applications submitted under 35 U.S.C. 371, where the “Sequence Listing” is…

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