Ex Parte Yakhini et alDownload PDFPatent Trial and Appeal BoardJun 8, 201610817244 (P.T.A.B. Jun. 8, 2016) Copy Citation UNITED STA TES p A TENT AND TRADEMARK OFFICE APPLICATION NO. FILING DATE 10/817,244 0410312004 22878 7590 06/10/2016 Agilent Technologies, Inc, in care of: CPA Global P. 0. Box 52050 Minneapolis, MN 55402 FIRST NAMED INVENTOR Zohar Y akhini UNITED STATES DEPARTMENT OF COMMERCE United States Patent and Trademark Office Address: COMMISSIONER FOR PATENTS P.O. Box 1450 Alexandria, Virginia 22313-1450 www .uspto.gov ATTORNEY DOCKET NO. CONFIRMATION NO. 10020503-2 3028 EXAMINER NEGIN, RUSSELL SCOTT ART UNIT PAPER NUMBER 1631 NOTIFICATION DATE DELIVERY MODE 06/10/2016 ELECTRONIC Please find below and/or attached an Office communication concerning this application or proceeding. The time period for reply, if any, is set in the attached communication. Notice of the Office communication was sent electronically on above-indicated "Notification Date" to the following e-mail address( es): IPOPS.LEGAL@agilent.com Agilentdocketing@cpaglobal.com PTOL-90A (Rev. 04/07) UNITED STATES PATENT AND TRADEMARK OFFICE BEFORE THE PATENT TRIAL AND APPEAL BOARD Ex parte ZOHAR Y AKHINI, ROBERT KINCAID, AMIR BEN-DOR, LESLIE A. LEONARD, and NICHOLAS M. SAMP AS Appeal2013-004406 1 Application 10/81 7 ,244 Technology Center 1600 Before DONALD E. ADAMS, DEMETRA J. MILLS, and FRANCISCO C. PRATS, Administrative Patent Judges. PRATS, Administrative Patent Judge. DECISION ON APPEAL This appeal under 35 U.S.C. § 134(a) involves claims to computer implemented methods for overlaying gene-related data onto chromosome maps. The Examiner rejected the claims for obviousness. We have jurisdiction under 35 U.S.C. § 6(b). We reverse. 1 Agilent Technologies, Inc., is the real party in interest. App. Br. 1. Appeal2013-004406 Application 10/81 7 ,244 STATEMENT OF THE CASE Claim 1 illustrates the appealed subject matter, and reads as follows (App. Br. 37): 1. A computer-implemented method for overlaying gene- or protein-related data on chromosome maps to provide at least one data-enhanced chromosome map as an output, said method compnsmg: receiving said chromosome maps as a first input to a computer; receiving a list comprising a plurality of gene- or protein- related data items as a second input to said computer, each data item including data other than data specifying a genetic location on said chromosome maps; providing an identifier specifying a genetic location for each of said data items on said chromosome maps; matching said identifiers with predefined identifiers on at least one of said chromosome maps; reordering said data items to an order matching the order of said predefined identifiers on said at least one of said chromosome maps; and displaying said data items on said at least one chromosome map at locations determined by said reordered data items to provide said data-enhanced output, wherein said receiving, matching, reordering and displaying are carried out automatically by said computer. The following rejections are before us for review: (1) Claims 1-3, 12-15, 21-23, 29, 55, and 56, under 35 U.S.C. § 103(a), for obviousness over Haefliger,2 Willecke,3 Cuticchia,4 Ledley,5 and Metaphase Chromosome Spread6 (Final Action 3-10);7 2 Jacques-Antoine Haefliger et al., Four Novel Members of the Connexin Family of Gap Junction Proteins, 267 J. Biol. Chem. 2057-2064 (1992). 2 Appeal2013-004406 Application 10/81 7 ,244 (2) Claims 4--10, under 35 U.S.C. § 103(a), for obviousness over Haefliger, Willecke, Cuticchia, Ledley, Metaphase Chromosome Spread, and Koleszar8 (Final Action 13-15); (3) Claim 11, under 35 U.S.C. § 103(a), for obviousness over Haefliger, Willecke, Cuticchia, Ledley, Metaphase Chromosome Spread, Koleszar, and Corcoran9 (Final Action 16-17); (4) Claims 16-18, 24--28, 30, 32, and 33, under 35 U.S.C. § 103(a), for obviousness over Haefliger, Willecke, Cuticchia, Ledley, Metaphase Chromosome Spread, and Golub 10 (Final Action 17-21 ); (5) Claims 19, 31, 34, 35, 80, and 81, under 35 U.S.C. § 103(a), for obviousness over Haefliger, Willecke, Cuticchia, Ledley, Metaphase Chromosome Spread, Golub, Lowe, 11 and Schultz12 (Final Action 23-25); 3 Klaus Willecke et al., Six genes of the human connexin gene family coding for gap junctional proteins are assigned to four different human chromosomes, 53 Eur. J. Cell. Biol. 275-280 (1990). 4 A.J. Cuticchia et al., CMAP: contig mapping and analysis package, a relational database for chromosome reconstruction, 8 CABIOS 467--474 (1992). 5 US Patent No. 4,656,594 (issued Apr. 7, 1987). 6 Definition of "metaphase chromosome spread," Dictionary of Developmental Biology and Embryology (2002) (http://www. credoreference. com/ entry /wileydevbio/ metaphase_chromosome_spread). 7 Final Action entered April 6, 2012. 8 US Patent No. 6,519,583 Bl (issued Feb. 11, 2003). 9 US Patent App. Pub. No. 2003/0224419 Al (published Dec. 4, 2003). 10 T. R. Golub et al., Molecular Classification of Cancer: Class Discovery and Class Prediction by Gene Expression Monitoring, 286 Science 531-537 (1999). 11 US Patent App. Pub. No. 2002/0081597 Al (published June 27, 2002). 12 US Patent No. 6,391,551 Bl (issued May 21, 2002). 3 Appeal2013-004406 Application 10/81 7 ,244 (6) Claims 44, 45, 47, 48, 90, 93, 94, and 101, under 35 U.S.C. § 103(a), for obviousness over Haefliger, Willecke, Cuticchia, Ledley, Metaphase Chromosome Spread, Golub, Lowe, Schultz, and Pollack13 (Final Action 27-29); and (7) Claims 46 and 92, under 35 U.S.C. § 103(a), for obviousness over Haefliger, Willecke, Cuticchia, Ledley, Metaphase Chromosome Spread, Golub, Lowe, Schultz, Pollack, and Vanhooydonck14 (Final Action 30-31 ). OBVIOUSNESS The Examiner's Position The Examiner cited Haefliger as disclosing a study of rat connexin (gap junction) proteins, in which each of four newly discovered connexin proteins was distinctly identified according to molecular weight, and their corresponding gene locations placed on mouse chromosomal maps. Final Action 4--5 (citing Haefliger, Fig. 6). The Examiner noted that Haefliger also placed, on those chromosomal maps, identifiers of the corresponding human genes, as well as identifiers providing the locations of the human genes on the human chromosomes. Id. at 5. The Examiner noted also that Haefliger cited Willecke as its source of information regarding the human connexin genes, and the Examiner cited Willecke for its disclosure of the human chromosomal locations of the corresponding human connexin genes. Id. at 6. 13 Jonathan R. Pollack et al., Genome-wide analysis of DNA copy-number changes using cDNA microarrays, 23 Nature Genetics 41--46 (1999). 14 US Patent No. 6,682, 172 B2 (issued Jan. 27, 2004). 4 Appeal2013-004406 Application 10/81 7 ,244 While the Examiner found that Haetliger and Willecke at least suggested claim 1 's step of reordering data items, the Examiner conceded that those reference "do not teach inputting the chromosomal maps into a computer. Haefliger et al. and Willecke et al. do not teach the computer limitations of the instantly rejected claims." Id. To address those deficiencies, the Examiner cited Ledley and Cuticchia. Id. at 6-7. As to Ledley, the Examiner contended: It would have been ... obvious to one of ordinary skill in the art at the time of the instant invention to modify the mouse chromosomal maps of Haefliger et al. and the human chromosomal mapping of Willecke et al. by use of function of inputting chromosomal maps into computer systems as in Ledley wherein the motivation would have been that entering chromosomal maps into a computerized system facilitates automated chromosomal analysis and interaction with the operator of the computer [column 3, line 59 to column 4, line 24 of Ledley]. Tri <>f 0 _LU. UL _/ • As to Cuticchia, the Examiner contended: It would have been further obvious to one of ordinary skill in the art at the time of the instant invention to modify the mouse chromosomal maps of Haefliger et al., the human chromosomal mapping of Willecke et al., and the inputting of chromosomal maps of Ledley by use of the computer equipment of Cuticchia et al. wherein the motivation would have been that the computers of Cuticchia et al. automate and expedite results [the first two paragraphs under "System and methods" on pages 467 to 468 of Cuticchia et al.]. Id. at 9-10. 5 Appeal2013-004406 Application 10/81 7 ,244 Analysis As stated in In re Oetiker, 977 F.2d 1443, 1445 (Fed. Cir. 1992): [T]he examiner bears the initial burden . . . of presenting a prim a facie case of unpatentability .... After evidence or argument is submitted by the applicant in response, patentability is determined on the totality of the record, by a preponderance of evidence with due consideration to persuasiveness of argument. In the instant case, we are not persuaded that the preponderance of the evidence supports the Examiner's prima facie case of obviousness. Independent claims 1 and 80 recite a computer implemented method that includes a step of receiving chromosome maps as a first input into a computer, and both of those claims recite that the receiving step is "carried out automatically by said computer." App. Br. 37, 42. The other independent claim on appeal, claim 101, similarly recites: receiving a list comprising a plurality of gene- or protein- related data items as an input to a computer, each data item having identifiers specifying a genetic location for each of said data items on said chromosome maps . . ., wherein said receiving ... [is] carried out automatically by said computer ... Id. at 43. As seen above, the Examiner relied initially on Ledley as providing the methodology and motivation for automatically inputting Haefliger's chromosome map, which included Willecke' s human connexin gene data, into a computer, as required by independent claims 1, 80, and 101. We agree with Appellants (App. Br. 18) that the Examiner has not explained adequately why an ordinary artisan would have applied the teachings of Ledley to the Haefliger' s chromosomal maps. 6 Appeal2013-004406 Application 10/81 7 ,244 As is evident, Haetliger's chromosomal maps consist of vertical lines along which are indicated the relative chromosomal positions of the genes encoding the connexin proteins that were discovered, as well as the positions on the human chromosome of the corresponding human genes. Haefliger, 2062 (Fig. 6). Haefliger, thus explains that "[t]he position of loci in human chromosomes, determined in previously reported studies, are shown to the right of the chromosome maps." Id. (Fig. 6 legend). In contrast to Haefliger' s use of maps to schematically depict chromosomes and the location of specific genes on those chromosomes, Ledley describes methods that automate the process of producing a karyotype, which involves generating direct visual images of chromosomes when viewed from a microscope. Ledley, col. 1, 11. 8-14; id. at col. 3, 1. 45 through col. 4, 1. 23. Ledley's invention seeks to improve the karyotyping process by providing an automated detector that detects, from an image of chromosomes obtained from the tested individual, a chromosome spread suitable for karyotyping: When a good metaphase spread comes into view under the microscope and TV camera 24 (via optical path 36), presence of the good metaphase spread is detected by metaphase detector 30 (connected to the microscope and TV camera 24 via optical path 44), and the computer system 20 is notified by metaphase detector 30 via the generation of output 46. Id. at col. 3, 11. 59---65 (bolding omitted). We are not persuaded that the Examiner has adequately explained why Ledley's teachings, directed to automated visual recognition of chromosome metaphase spreads using a microscope, with no mention of being able to locate the positions of any specific genes on the chromosome, 7 Appeal2013-004406 Application 10/81 7 ,244 would have prompted an ordinary artisan to automatically input, into a computer, Haefliger's maps, which schematically depict chromosomes and the location of specific genes on those chromosomes. As noted above, the Examiner contends that "the motivation would have been that entering chromosomal maps into a computerized system facilitates automated chromosomal analysis and interaction with the operator of the computer [column 3, line 59 to column 4, line 24 of Ledley]." Final Action 9. The Examiner does not direct us, however, to any evidence in that passage or any other portion of Ledley suggesting that Ledley's system is capable of, or suitable for, analyzing the type of data presented in the chromosomal maps of Haefliger. As noted above, the Examiner also appears to rely on Cuticchia as suggesting the automated step of receiving Haefliger's chromosomal maps as an input to a computer, as required by claims 1, 80, and 101, the independent claims under appeal. Final Action 9-10; see also Ans. 7 ("[T]he documents of Ledley and Cuticchia et al. not only teach obviousness of automation of such a plot [as Figure 6 of Haefliger], but the documents also teach obviousness of inputting and outputting data from related diagrams into computer systems."). While the Examiner directs us to certain passages within Cuticchia to support his indicated rationale, the Examiner does not identify or discuss specifically which teachings within those passages support that rationale, or suggest the automated step of receiving Haefliger's chromosomal maps as an input to a computer. In particular, the Examiner contends that "the motivation would have been that the computers of Cuticchia et al. automate 8 Appeal2013-004406 Application 10/81 7 ,244 and expedite results [the first two paragraphs under 'System and methods' on pages 467 to 468 of Cuticchia et al.]." We acknowledge that the cited passage on pages 467--468 of Cuticchia discusses how users may input gene sequence data into a database to create a sequential map of clones or gene fragments. Cuticchia 468 ("Once an order of fragments has been reached, CMAP [the contig mapping and analysis package] can update 'to' and 'from' clone pointers via SQL [structured query language] to create the linear arrangement representing the contig map within the database."); see also id. at 4 72, left column (discussing how users input sequence data into the database). The Examiner does not, however, explain with adequate specificity how or why these passages of Cuticchia, or any other portions of the reference, suggest that the results of Haefliger' s chromosomal mapping of connexin genes might be expedited or automated, as the Examiner posits. The Examiner also does not explain specifically why an ordinary artisan would have viewed the nucleotide sequence-related techniques described in Cuticchia as being applicable to the chromosomal mapping experiments described in Haefliger, or how, specifically, Haefliger would have been modified to incorporate Cuticchia's teachings to arrive at a process including the automated step of receiving chromosomal maps as an input to a computer, as required by independent claims 1, 80, and 101 under appeal herein. Accordingly, we are not persuaded that the Examiner has adequately explained why the combination of Haefliger, Willecke, Ledley, and Cuticchia, as posited, teaches or suggests the automated step of receiving chromosomal maps as an input to a computer, as required by claims 1, 80, 9 Appeal2013-004406 Application 10/81 7 ,244 and 101, the independent claims under appeal. Because we are not persuaded that the Examiner has adequately explained why the combination of Haefliger, Willecke, Ledley, and Cuticchia teaches or suggests all of the steps required by claims 1, 80, and 101, and because each of the Examiner's rejections relies ultimately on that combination of references to render obvious the processes recited in those claims, we reverse each of the Examiner's rejections. SUMMARY For the reasons discussed, we reverse each of the Examiner's obviousness rejections. REVERSED 10 Copy with citationCopy as parenthetical citation