GAJARSA, Circuit Judge.
This is an appeal from a decision of the Board of Patent Appeals and Interferences (“Board”) in Interference No. 105,187, declared on December 24, 2003, between Falkner
et al,
U.S. Patent No. 5,770,212 (“the Falkner ’212 patent”) and Inglis
et al,
U.S. Application Serial No. 08/459,040 (“the Inglis ’040 application”). The Administrative Patent Judge (APJ) designated Inglis as the senior party. On December 29, 2004, the Board issued a final decision, holding that Falkner could not antedate Inglis’ September 25, 1990 priority date, and entered judgment against Falkner on the sole count of the interference. It ordered that Falkner was not entitled to claims 1-19 of the Falkner ’212 patent. It further ordered that Inglis was entitled to claims 9, 10, 29 and 30 of the ’040 application. Falkner filed a timely notice of appeal. This Court has jurisdiction pursuant to 28 U.S.C. § 1295(a)(4)(A) and 35 U.S.C. §§ 141 and 142. For the reasons discussed below, we affirm the judgment of the Board.
I. BACKGROUND
A. The Invention
Some vaccines against a virus (the “target virus”) incorporate harmless fragments of the target virus’s genetic material into a second virus, called a “viral vector.” When a person is vaccinated, the viral vector produces harmless fragments of the target virus, ultimately conferring immunity against it. To prevent the viral vector from itself causing a harmful infection in
the inoculee, it must be attenuated. Attenuation is achieved by deleting or inactivating one or more genes responsible for the vector’s growth and infectiousness. However, because the vaccine is produced by essentially “growing” the vector virus (accompanied by its inserted target virus gene), attenuation makes it difficult to manufacture the vaccine. The traditional solution to this problem has been to inactivate genes known as “inessential” genes. With inessential genes inactivated, the viral vector is substantially less pathogenic. At the same time, because the vector virus can still fully reproduce itself, albeit more slowly, the vaccine can be produced in commercial quantities. However, the traditional approach carried a disadvantage, namely the risk that the vector virus, though attenuated, could still cause a harmful infection in the inoculee.
The inventors discovered a way of making vaccines safer by deleting or inactivating an
essential,
rather than an inessential, gene from the viral vector’s genome, while at the same time solving the production problem by growing the vaccines in cells that were complementarily modified to produce the absent essential viral gene product “on behalf of’ the vector virus. Thus, the modified vector virus could be readily grown in these complementarily-modified cells, but not in other cells, such as those of an inoculee.
This approach is applicable to many different kinds of vector viruses, e.g., ade-noviruses, herpesviruses, poxviruses and retroviruses. The subject matter of this interference, however, is directed specifically to vaccines in which the vector virus is a
poxvirus.
For many vector viruses, there is a risk that vectors that have been attenuated in essential genes can “swap” genes with the host cell genome, thereby reacquiring their deleted genes and reverting to wild-type virus. This risk can be minimized through the use of viruses that are “cytoplasmic”, meaning that they are unlikely to enter the cell nucleus. Because a cell’s genes are located in the nucleus, cytoplasmic viruses such as poxvirus cannot swap genes with the cell genome and possibly revert to a virulent wild-type virus.
B. Defining the Count and Assigning Priority
The sole count of the interference was either “[a] vaccine according to Claim 1 of Falkner’s 5,770,212 patent or a vaccine according to Claim 29 of Inglis’ 08/459,040 application.” Claim 29 of the Inglis ’040 application reads:
A vaccine comprising a pharmaceutically acceptable excipient and an effective immunizing amount of a mutant virus, wherein said mutant virus is a mutant
poxvirus
and has a genome which has an inactivating mutation in a viral gene, said viral gene being essential for the production of infectious new virus particles, wherein said mutant virus is able to cause production of infectious new virus particles in a complementing host cell gene expressing a gene which complements said essential viral gene, but is unable to cause production of infectious new virus particles when said mutant virus infects a host cell other than a complementing host cell; for prophylactic or therapeutic use in generating an immune response in a subject.
(emphasis added)
Claim 1 of the Falkner ’212 patent reads:
A vaccine comprising (a) a defective pox-virus that lacks a function imparted by an essential region of its parental poxvi-rus, wherein (i) said defective poxvirus comprises a DNA polynucleotide encoding an antigen and said DNA polynu-cleotide is under transcriptional control of a promoter, and (ii) the function can
be complemented by a complementing source; and (b) a pharmaceutically acceptable carrier.
The Administrative Patent Judge (APJ) designated claims 1-19 of the Falkner ’212 patent and claims 9, 10, 29, and 30 of the Inglis ’040 application as corresponding to the interference count.
Both parties sought the benefit of earlier-filed applications to establish dates of constructive reduction to practice.
The ALJ accorded the Inglis ’040 application (filed June 2, 1995) the benefit of several earlier-filed applications, dating back to September 25,1990.
Likewise, the APJ accorded the Falkner ’212 patent (issued June 23, 1998 from an application filed February 21, 1997) the benefit of earlier-filed applications, but these dated back only to April 29, 1994.
Consequently, the APJ designated Inglis as the senior party.
C. Board Decision
The specifications of all of Inglis’ earlier applications were similar. Although they focused on herpesvirus vectors, they contained several passages related to pox-virus-based vaccines. Because Falkner believed that these passages did not adequately describe and enable the poxvirus invention, he challenged both Inglis’ entitlement to priority as to the count and the patentability of Inglis’ corresponding claims. Falkner brought these challenges
in three closely-related preliminary motions before the Board. In each, as the moving party, Falkner carried the burden of proof by a preponderance of the evidence.
See
37 C.F.R. § 1.637(a);
see also Kubota v. Shibuya,
999 F.2d 517, 520 n. 2 (Fed.Cir.1993) (explaining that “[t]he term ‘burden of proof ... means the burden to establish the proposition at issue by a preponderance of the evidence”).
Falkner brought his first preliminary motion pursuant to 37 C.F.R. § 1.633(a),
arguing that the claims in Inglis’s involved (’040) application that corresponded to the count were unpatentable because they failed to meet the written description requirement of 35 U.S.C. § 112. In support of his argument, he stated,
inter alia,
that (1) the specification of Inglis’s ’040 application did not identify any essential genes in poxvirus or describe the inactivation of such genes, (2) vaccines based on vaccinia (a type of poxvirus) had not yet been produced, and (3) the bulk of the Inglis specification was directed not to poxviruses but to herpesviruses. The Board denied Falk-ner’s motion, based in part on his failure to address the perceived shortcomings of the ’040 claims in light of the specification.
Second, Falkner moved pursuant to 37 C.F.R. §§ 1.633(g) & 1.637(g) to deny In-glis the priority benefit of his earlier applications, arguing that they did not sufficiently describe and enable the claims in question.
Falkner argued that without the benefit of these applications Inglis would be unable to establish constructive reduction to practice earlier than Falkner. Falkner would win priority as to the count, and Inglis’ corresponding claims would be unpatentable. In support of his motion, Falkner alleged deficiencies in In-glis’ benefit specifications similar to those raised in his first motion. The Board carefully articulated the legal standard, correctly explaining that “benefit with respect to priority in an interference is granted with respect to
counts
not
claims
” and that “[a]ll that is necessary for a party to be entitled to benefit of an earlier filed application for priority purposes is compliance with 35 U.S.C. § 112 with respect to at least one embodiment within the scope of the count.”
Board Op.
at 7 (citing
Hunt v. Treppschuh,
523 F.2d 1386, 1389 (CCPA 1975) (holding that where a “parent application is relied upon as a prior constructive reduction to practice[,] .... the § 112, first paragraph requirements need only be met for an embodiment within the count”)). After careful review of the record, the Board held that Falkner had failed to meet his burden of proof.
Third, Falkner moved for judgment pursuant to 37 C.F.R. § 1.633(a) that the claims in Inglis’ involved (’040) application that corresponded to the count were anticipated and therefore unpatentable. He argued that because Inglis’ earlier applications had failed to adequately describe and enable the full scope of his current claims, the current claims could not be accorded the benefit of 35 U.S.C. § 120 for the
purpose of antedating patent-defeating pri- or art.
The Board explained that 35 U.S.C. §§ 119 & 120 require benefit applications to comply with § 112, first paragraph, with respect to the
full scope
of what a party now claims, rather than with respect to merely one embodiment within the scope of the interference count. After carefully considering the written description and enablement issues, the Board denied the motion. As a result of the denial of Falkner’s several motions, Inglis remained the senior party, and the Board ordered judgment as to the subject matter of the count in favor of Inglis.
D. Issue and Standard of Review
On appeal, Falkner essentially reiterates the arguments that he made before the Board. While we recognize that each of these three arguments is distinct, they are nonetheless all related, and under the facts of this particular case, we need only to resolve the following common issue: whether the Inglis benefit applications adequately describe and enable a poxvirusbased vaccine. Falkner also argues that the Board committed other errors, such as initially designating Inglis as the senior party and failing to afford Falkner an opportunity for briefing prior to making this designation. These arguments lack merit, and we shall not further discuss them. We turn, therefore, to the central issues in this case: written description and enablement.
Written description is a question of fact, judged from the perspective of one of ordinary skill in the art as of the relevant filing date.
See Vas-Cath, Inc. v. Mahurkar,
935 F.2d 1555, 1563-64 (Fed. Cir.1991). Enablement is a question of law involving underlying factual inquiries.
See Genentech, Inc. v. Novo Nordisk A/S,
108 F.3d 1361, 1365 (Fed.Cir.1997);
see also In re Wands,
858 F.2d 731, 737 (Fed. Cir.1988) (holding that whether undue experimentation is required is a “conclusion reached by weighing many factual considerations .... including] (1) the quantity of experimentation necessary, (2) the amount of direction or guidance presented, (3) the presence or absence of working examples, (4) the nature of the invention, (5) the state of the prior art, (6) the relative skill of those in the art, (7) the predictability or unpredictability of the art, and (8) the breadth of the claims.”).
This court applies the standards of the Administrative Procedure Act (“APA”) in reviewing decisions of the Board.
See Dickinson v. Zurko,
527 U.S. 150, 152, 119 S.Ct. 1816, 144 L.Ed.2d 143 (1999) (holding that 5 U.S.C. § 706 governs our review of PTO appeals). Accordingly, we will set aside actions of the Board if they are arbitrary, capricious, an abuse of discretion, or otherwise not in accordance with law, and we set aside factual findings that are unsupported by substantial evidence.
See In re McDaniel,
293 F.3d 1379, 1382 (Fed.Cir.2002) (citing 5 U.S.C. § 706);
see also In re Sullivan,
362 F.3d 1324, 1326 (Fed.Cir.2004) (substantial evidence review of factual findings). We review questions of law
de novo. See Rapoport v. Dement,
254 F.3d 1053, 1058 (Fed.Cir.2001).
Substantial evidence is defined as that which a reasonable person might accept as adequate to support a conclusion.
See In re Zurko,
258 F.3d 1379, 1384 (Fed. Cir.2001). It requires an examination of the record as a whole, taking into account both the evidence that justifies and detracts from an agency’s opinion.
See In re Gartside,
203 F.3d 1305, 1312 (Fed.Cir.
2000). An agency decision can be supported by substantial evidence, even where the record will support several reasonable but contradictory conclusions.
See id.; see also In re Jolley,
308 F.3d 1317, 1320 (Fed.Cir.2002).
II. DISCUSSION
A. Contents of the Inglis Priority Applications
The claims that correspond to the count of the interference are directed to a novel type of vaccine that is comprised of a “vector virus” in the poxvirus family. Conceptually, poxviruses are a “subgenus” of viruses that includes the “species” vacci-nia. All of the prior Falkner applications described poxvirus vaccine vectors in detail, and to the exclusion of other types of vaccine vectors (e.g., herpesvirus vaccine vectors). These applications provided five detailed working examples regarding the preparation and use of vaccines from defective poxviruses. They also described the use of a particular species of poxvirus vaccine vector, namely vaccinia virus.
In contrast, the Inglis applications described vaccine vectors in general, and then focused on the subgenus of herpesvi-ruses, for which they provided a detailed example. Nevertheless, at least three passages discussed the poxvirus invention and specifically mentioned “vaccinia virus.”
For example, after introducing the concept of vaccine vectors, the specification states that “[t]ypically members of the pox virus family, e.g. vaccinia virus, are used as vaccine vectors.”
The specification later discusses the deletion of essential genes from vaccine vector genomes, noting that the “invention can be applied to
any virus
where one or more essential gene(s) can be identified and deleted from or inactivated within the virus genome” (emphasis added). . Moreover, it provides that “the virus may comprise an orthopox virus, for example, vaccinia virus, which may comprise a heterologous sequence encoding an immu-nogen derived from a pathogen.” Finally, it reads:
For example vaccinia virus, a poxvirus, can carry and express genes from various pathogens, and it has been demonstrated that these form effective vaccines when used in animal experimental systems. The potential for use in humans is vast, but because of the known side effects associated with the widespread use of vaccinia as a vaccine against smallpox, there is reluctance to use an unmodified vaccine in humans. There have been attempts to attenuate vaccinia virus by deleting non-essential genes such as the vaccinia growth factor gene... However, such attenuated viruses can still replicate in vivo, albeit at a reduced level. No vaccinia virus with a deletion in an essential gene has yet been produced, but such a virus, deleted in an essential gene as described above, with its complementing cell for growth, would provide a safer version of this vaccine.
The application provides a detailed example of an embodiment that comprised not a poxvirus, but a
herpesvirus,
includ
ing the identity of the deleted essential sequences therein. Nevertheless, for the reasons discussed below, we find no error in the Board’s determinations on the adequacy of written description and enablement in the various Inglis disclosures.
B. Enablement
Because the adequacy of the disclosure is judged from the perspective of one of ordinary skill in the art, we start our review of the Board’s decision by noting that the parties stipulated to a high level of skill in the art. They defined the skilled artisan as having 5-10 years experience creating recombinant poxvirus, as being familiar with the poxvirus literature, the use of poxvirus as a vector for the expression of heterologous genes, and having the “needed technical skill to practice the experimentation described in the scientific literature relating to recombinant virus, including poxvirus.” The Board agreed with the parties’ stipulation as to level of skill.
The Board did not err in finding Inglis’ claims to be enabled as a matter of law, in light of its articulated underlying factual findings. In support of its conclusion, it noted that “there is extensive disclosure of the selection of an essential gene, its deletion or inactivation and the production of a mutated virus with said deleted or inactivated gene, albeit for herpesvirus.” Moreover, because the differences between the herpesviruses and poxviruses were well known, this would have aided the person of ordinary skill in the art in her application of the lessons of the herpesvirus example in the construction of poxvirus vaccines. The Board observed that “the mere fact that the experimentation may have been difficult and time consuming does not mandate a conclusion that such experimentation would have been considered to be ‘undue’ in this art. Indeed, great expenditures of time and effort were ordinary in the field of vaccine preparation.” Thus, the Board found the Inglis applications to be enabling.
Reviewing the Board’s legal conclusion of enablement, as based on its underlying findings of fact, we cannot say that the Board erred. With respect to a skilled artisan’s ability to identify “essential” pox-virus genes, as discussed below we note that there was undisputed testimony that as of the time of filing of the earliest Inglis application publications in professional journals had disclosed the DNA sequence of the poxvirus genome along with the locations of the “essential regions.” The person of ordinary skill in the art would clearly have possessed such knowledge, and given the ready accessibility of the journals, the absence of incorporation by reference is not problematic. Indeed, “[a] patent need not teach, and preferably omits, what is well known in the art.”
Spectra-Physics, Inc. v. Coherent, Inc.,
827 F.2d 1524, 1534 (Fed.Cir.1987).
C. Written Description
On appeal to this court, Falkner essentially reargues the positions on written description that he took before the Board. Although the Board erred in its articulation of the written description standard, that error is harmless. The Board held that “an actual possession standard is
not
required.” (emphasis added). But our precedent clearly establishes that “[t]he applicant must ... convey to those skilled in the art that, as of the filing date sought, he or she was in possession of the invention.”
Vas-Cath, Inc. v. Mahurkar,
935 F.2d 1555, 1563-64 (Fed.Cir.1991). Nonetheless, we conclude there is no need for remand because the undisputed testimony supports the Board’s ultimate conclusion.
As noted above, the Board found several passages in the Inglis ’040 application (and in the benefit applications) that were directed to poxvirus. No length requirement exists for a disclosure to ade
quately describe an invention.
See In re Hayes Microcomputer Prods., Inc. Patent Litig.,
982 F.2d 1527, 1534 (Fed.Cir.1992) (“[T]he adequacy of the description of an invention depends on its content in relation to the particular invention, not its length.”). Furthermore, the testimony of Inglis’ expert, Dr. Boursnell, established that the articles describing essential genes for poxvirus were well-known in the art. Dr. Boursnell testified that “the skilled person would have been readily able to choose an essential vaccinia gene” based on references that have been publicly available since 1990. The testimony of Falkner’s expert, Dr. Carroll, did not refute this claim.
The parties also dispute several aspects of our law of written description, which we now address. We conclude that the Board applied correct law. Specifically, we hold, in accordance with our prior case law, that (1) examples are not necessary to support the adequacy of a written description (2) the written description standard may be met (as it is here) even where actual reduction to practice of an invention is absent; and (3) there is no
per se
rule that an adequate written description of an invention that involves a biological macromolecule must contain a recitation of known structure.
1. Examples Are Not Required
First, it is clear that the absence of examples involving poxviruses in the Inglis applications does not render the written description inadequate. As we explained in
LizardTech, Inc. v. Earth Resource Mapping, PTY, Inc.:
A claim will not be invalidated on section 112 grounds simply because the embodiments of the specification do not contain examples explicitly covering the full scope of the claim language. That is because the patent specification is written for a person of skill in the art, and such a person comes to the patent with the knowledge of what has come before. Placed in that context, it is unnecessary to spell out every detail of the invention in the specification; only enough must be included to convince a person of skill in the art that the inventor possessed the invention and to enable such a person to make and use the invention without undue experimentation.
424 F.3d 1336, 1345 (Fed.Cir.2005) (citing
Union Oil Co. v. Atl. Richfield Co.,
208 F.3d 989, 997 (Fed.Cir.2000);
In re GPAC Inc.,
57 F.3d 1573, 1579 (Fed.Cir.1995)).
2. Actual Reduction to Practice Is Not Required
As we explained in
Capon v. Eshhar,
“[t]he ‘written description’ requirement implements the principle that a patent must describe the technology that is sought to be patented; the requirement serves both to satisfy the inventor’s obligation to disclose the technologic knowledge upon which the patent is based, and to demonstrate that the patentee was in possession of the invention that is claimed.” 418 F.3d 1349, 1357 (Fed.Cir. 2005). The Board was correct, however, not to view as dispositive that Inglis had not actually
produced
a poxvirus vaccine,
because an actual reduction to practice is not required for written description.
See
Univ. of Rochester v. G.D. Searle & Co.,
358 F.3d 916, 926 (Fed.Cir.2004) (“We of course do not mean to suggest that the written description requirement can be satisfied only by providing a description of an actual reduction to practice. Constructive reduction to practice is an established method of disclosure .... ”).
Rochester,
moreover, is consistent with Supreme Court precedent. In the context of interpreting 35 U.S.C. § 102(b), the Court held that “[t]he word ‘invention’ must refer to a concept that is complete, rather than merely one that is ‘substantially complete.’ ”
Pfaff v. Wells Elecs.,
525 U.S. 55, 66, 119 S.Ct. 304, 142 L.Ed.2d 261 (1998). It then proceeded to make clear that although “reduction to practice ordinarily provides the best evidence that an
invention
is complete.... it does not follow that proof of reduction to practice is necessary in every case.”
Id.
(emphasis added).
Thus, to the extent that written description requires a showing of “possession of the invention,”
Capon,
418 F.3d at 1357 (emphasis added),
Pfaff
makes clear that an invention can be “complete” even where an
actual
reduction to practice is absent.
The logical predicate of “possession” is, of course, “completeness.”
3. Recitation of Known Structure Is Not Required
Falkner argues,
inter alia,
that the Inglis specifications do not adequately describe the poxvirus invention, in light of
Eli Lilly,
because they do not describe the “essential regions” of any poxvirus. 119 F.3d 1559. We note, in addition, that In-glis did not attempt to incorporate by reference any literature that described the DNA sequence of the poxvirus genome and the locations of the “essential regions.” However, it is the binding precedent of this court that
Eli Lilly
does
not
set forth a
per se
rule that whenever a claim limitation is directed to a macromolecular sequence, the specification must always recite the gene or sequence, regardless of whether it is known in the prior art.
See Capon, 418
F.3d at 1357 (“None of the cases to which the Board attributes the requirement- of total DNA re-analysis, i.e.,
Regents v. Lilly, Fiers v. Revel, Amgen,
or
Enzo Biochem,
require a re-description of what was already known.”). Thus, “[w]hen the prior art includes the nucleotide information, precedent does not set a
per se
rule that the information must be determined afresh.”
Id.
at 1358. Rather, we explained that:
The descriptive text needed to meet these requirements varies with the nature and scope of the invention at issue, and with the scientific and technologic knowledge already in existence. The law must be applied to each invention that enters the patent process, for each patented advance is novel in relation to the state of the science. Since the law is applied to each invention in view of the state of relevant knowledge, its application will vary with differences in the
state of knowledge in the field and differences in the predictability of the science.
Id.
at 1357.
Indeed, a requirement that patentees recite known DNA structures, if one existed, would serve no goal of the written description requirement. It would neither enforce the quid pro quo between the pat-entee and the public by forcing the disclosure of new information, nor would it be necessary to demonstrate to a person of ordinary skill in the art that the patentee was in possession of the claimed invention. As we stated in
Capon,
“[t]he ‘written description’ requirement states that the patentee must describe the invention; it does not state that every invention must be described in the same way. As each field evolves, the balance also evolves between what is known and what is added by each inventive contribution.”
Id.
at 1358. Indeed, the forced recitation of known sequences in patent disclosures would only add unnecessary bulk to the specification. Accordingly we hold that where, as in this case, accessible literature sources clearly provided, as of the relevant date, genes and their nucleotide sequences (here “essential genes”), satisfaction of the written description requirement does not require either the recitation or incorporation by reference
(where permitted) of such genes and sequences.
In conclusion, having reviewed the decision of the Board, we can discern no error in its conclusion that the disclosures relied upon by Inglis for priority purposes adequately described and enabled the invention directed to poxvirus, there being substantial evidence to support these findings. Consequently, we hold that the Board’s award of priority to Inglis was proper.
AFFIRMED
No costs.