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EUTM file information

018512976

BIOSKRYB GENOMICS


July 12, 2021

Trademark Summary

The trademark application BIOSKRYB GENOMICS was filed by BioSkryb Genomics, Inc., a U.S. corporation (the "Applicant"). The application was published for oppositions on October 21, 2021, and it was registered by office on January 28, 2022 without any oppositions.

The application was filed in English (German was selected as the second language).

Change of name and address of the trademark registration was recorded on October 6, 2021.


Goods And Services

  • The mark was filed in class 1 with following description of goods:
    1. Assays and reagents for use in genetic research
    2. Diagnostic reagents for scientific, medical, and research use
    3. Diagnostic reagents for clinical or medical laboratory use
    4. Reagents and reagent kits
    5. Reagents for use in kits for high-quality single-cell and low-input DNA amplification, primary template-directed amplification (PTA) reaction and library cleanup, optimum bead cleanup performance, single-cell and low-input transcriptional profiling, and combined genome and transcriptome profiling
    6. Reagents and containers of reagents, namely, reagents comprising paramagnetic beads for use in the processing, purification, and cleanup of samples containing genomic material, including material from single cells, for medical and research purposes
    7. Reagents and containers of reagents, namely, reagents for use in the amplification and recovery of genomic material, including genomic material from single cells
    8. Chemical substances and products for use in genomic research
    9. Biochemicals, namely, biological reagents for use in whole genome amplification to detect genetic variants in each cell
    10. Laboratory chemicals, namely, an antibody reagent used for genomic research
    11. Chemical kits for diagnostic purposes for laboratory, medical, and research use
    12. Kits containing laboratory chemicals, namely, an antibody reagent used for genomic research.
  • The mark was filed in class 9 with following description of goods:
    1. Computer software
    2. Downloadable applications
    3. Downloadable computer software for collecting, analyzing, reporting, and tracking data and information in the fields of genetics, genomics, proteomics, transcriptomics, epigenomics, metabolomics, meta-genomics, meta-transcriptomics, and microbiomics
    4. Downloadable computer software for bioinformatic DNA sequencing analysis for the purpose of allowing users to evaluate data quality, compare results between cells and samples, and integrate multi-omics data
    5. Downloadable computer software for bioinformatic DNA sequencing analysis for evaluating data, namely, sequencing alignment, coverage, and single nucleotide, structural, and copy number variant calling metrics
    6. Downloadable computer software for genomic analysis and sequencing for scientific, medical, and research purposes
    7. Downloadable computer software for medical and scientific research in the fields of genetics, genomics, proteomics, transcriptomics, epigenomics, metabolomics, meta-genomics, meta-transcriptomics, and microbiomics
    8. Downloadable computer software for nucleic acid and ribonucleic acid analysis for medical and scientific research purposes
    9. Downloadable computer software for providing medical and scientific research information in the fields of genetics, genomics, proteomics, transcriptomics, epigenomics, metabolomics, meta-genomics, meta-transcriptomics, and microbiomics
    10. Downloadable computer software for medical and scientific research in connection with high-quality single-cell and low-input DNA amplification, primary template-directed amplification (PTA) reaction and library cleanup, optimum bead cleanup performance, single-cell and low-input transcriptional profiling, and combined genome and transcriptome profiling
    11. Downloadable computer software for medical and scientific research in connection with genome amplification to detect genetic variants in cells
    12. Downloadable computer software for medical and scientific research in connection with measuring genetic diversity in single cells
    13. Downloadable computer software for medical and scientific research in connection with primary template-directed amplification for use in connection with single cells and ultra-low DNA input samples
    14. Downloadable computer software for medical and scientific research for the purpose of elevating single cell genome variants for the purpose of genome amplification
    15. Downloadable computer software for DNA analysis and sequencing services for scientific, medical, and research purposes
    16. Downloadable computer software for research, development and consultancy in the field of genomics
    17. Downloadable computer software for compiling data for research purposes in the field of genomics
    18. Downloadable computer software for providing medical research information in the field of genomics, gene therapy, cell therapy for medical purposes
    19. Downloadable computer software for use in connection with medical testing, diagnosis, and treatment purposes
    20. Downloadable computer software for use in connection with offering medical analysis services for diagnostic and treatment purposes provided by medical laboratories
    21. Downloadable computer software for use in connection with medical diagnostic testing, monitoring, and reporting services
    22. Downloadable computer software for medical analysis and diagnostic services in connection with the fields of oncology, cardiology, prenatal genetic testing (PGT), neurological genetic disorders, immunology, microbiome, toxicology, and bioprocessing
    23. Downloadable computer software for medical analysis and diagnostic services in the field of gene therapy and cell therapy
    24. Downloadable computer software for medical analysis and diagnostic services in the fields of genetics, genomics, proteomics, transcriptomics, epigenomics, metabolomics, meta-genomics, meta-transcriptomics, and microbiomics
    25. Laboratory apparatus and instruments
    26. Laboratory apparatus and instruments, namely, genomic testing kits
    27. Laboratory apparatus and instruments for the amplification and recovery of genomic material, including genomic material from single cells
    28. Laboratory apparatus and instruments, namely, magnetic plates for use with magnetic and paramagnetic beads for the processing, purification, and cleanup of samples containing genomic material, including material from single cells
    29. Kits containing a scientific or laboratory apparatus or instrument, namely, kits comprising multi-well plates, magnetic plates, and reagents comprising paramagnetic beads for the processing, purification, and cleanup of samples containing genomic material, including material from single cells
    30. Kits comprising reagents and a scientific or laboratory apparatus or instrument for the amplification and recovery of genomic material, including genomic material from single cells.
  • The mark was filed in class 10 with following description of goods:
    1. Medical test kits for high-quality single-cell and low-input DNA amplification, primary template-directed amplification (PTA) reaction and library cleanup, optimum bead cleanup performance, single-cell and low-input transcriptional profiling, and combined genome and transcriptome profiling
    2. Diagnostic kits comprising of reagents for medical and scientific use
    3. Diagnostic kits comprised of reagents and assays for detecting, testing, analyzing, and sequencing genes, nucleic acids, and biological molecules
    4. Medical test kits for use in the amplification and recovery of genomic material, including genomic material from single cells
    5. Medical test kits comprised of biological reagents for use in whole genome amplification to detect genetic variants in cells
    6. Gene and genetic testing apparatus in the nature of apparatus for DNA and RNA testing for medical and scientific purposes
    7. Scientific, medical apparatus and instruments for the amplification and recovery of genomic material, including genomic material from single cells
    8. Scientific and medical apparatus and instruments, namely, magnetic plates for use with magnetic and paramagnetic beads for the processing, purification, and cleanup of samples containing genomic material, including material from single cells
    9. Kits comprising reagents, namely, reagents comprising paramagnetic beads for use in the processing, purification, and cleanup of samples containing genomic material, including material from singles, for medical and research purposes
    10. Kits containing assays, reagents, and chemical substances and products for use in genomic research
    11. Kits containing medical and scientific apparatus for use in genetic research
    12. Kits containing biochemicals, namely, biological reagents for use in whole genome amplification to detect genetic variants in each cell
    13. Kits for diagnostic purposes for laboratory, medical or research use.
  • The mark was filed in class 42 with following description of goods:
    1. Providing online non-downloadable software
    2. Software as a service (SaaS)
    3. Genomic analysis and sequencing services for scientific, medical, and research purposes
    4. Medical and scientific research in the fields of genetics, genomics, proteomics, transcriptomics, epigenomics, metabolomics, meta-genomics, meta-transcriptomics, and microbiomics
    5. Nucleic acid and ribonucleic acid analysis services for medical and scientific research purposes
    6. Providing medical and scientific research information in the fields of genetics, genomics, proteomics, transcriptomics, epigenomics, metabolomics, meta-genomics, meta-transcriptomics, and microbiomics
    7. Medical and scientific research in connection with high-quality single-cell and low-input DNA amplification, primary template-directed amplification (PTA) reaction and library cleanup, optimum bead cleanup performance, single-cell and low-input transcriptional profiling, and combined genome and transcriptome profiling
    8. Medical and scientific research in connection with genome amplification to detect genetic variants in cells
    9. Medical and scientific research in connection with measuring genetic diversity in single cells
    10. Medical and scientific research in connection with primary template-directed amplification for use in connection with single cells and ultra-low DNA input samples
    11. Medical and scientific research for the purpose of elevating single cell genome variants for the purpose of genome amplification
    12. DNA analysis and sequencing services for scientific, medical, and research purposes
    13. Research, development and consultancy in the field of genomics
    14. Medical research, namely, compiling data for research purposes in the field of genomics
    15. Providing medical research information in the field of genomics, gene therapy, cell therapy for medical purposes
    16. Providing on-line non-downloadable software for collecting, analyzing, reporting, and tracking data and information in the fields of genetics, genomics, proteomics, transcriptomics, epigenomics, metabolomics, meta-genomics, meta-transcriptomics, and microbiomics
    17. Platform as a service (PAAS) featuring computer software platforms for collecting, analyzing, reporting, and tracking data and information in the fields of genetics, genomics, proteomics, transcriptomics, epigenomics, metabolomics, meta-genomics, meta-transcriptomics, and microbiomics
    18. Software as a service (SAAS) services featuring software for collecting, analyzing, reporting, and tracking data and information in the fields of genetics, genomics, proteomics, transcriptomics, epigenomics, metabolomics, meta-genomics, meta-transcriptomics, and microbiomics
    19. Providing temporary use of non-downloadable computer software for bioinformatic DNA sequencing analysis for the purpose of allowing users to evaluate data quality, compare results between cells and samples, and integrate multi-omics data
    20. Providing temporary use of non-downloadable computer software for bioinformatic DNA sequencing analysis for evaluating data, namely, sequencing alignment, coverage, and single nucleotide, structural, and copy number variant calling metrics
    21. Providing temporary use of non-downloadable computer software for genomic analysis and sequencing for scientific, medical, and research purposes
    22. Providing temporary use of non-downloadable computer software for medical and scientific research in the fields of genetics, genomics, proteomics, transcriptomics, epigenomics, metabolomics, meta-genomics, meta-transcriptomics, and microbiomics
    23. Providing temporary use of non-downloadable computer software for nucleic acid and ribonucleic acid analysis for medical and scientific research purposes
    24. Providing temporary use of non-downloadable computer software for providing medical and scientific research information in the fields of genetics, genomics, proteomics, transcriptomics, epigenomics, metabolomics, meta-genomics, meta-transcriptomics, and microbiomics
    25. Providing temporary use of non-downloadable computer software for medical and scientific research in connection with high-quality single-cell and low-input DNA amplification, primary template-directed amplification (PTA) reaction and library cleanup, optimum bead cleanup performance, single-cell and low-input transcriptional profiling, and combined genome and transcriptome profiling
    26. Providing temporary use of non-downloadable computer software for medical and scientific research in connection with genome amplification to detect genetic variants in cells
    27. Providing temporary use of non-downloadable computer software for medical and scientific research in connection with measuring genetic diversity in single cells
    28. Providing temporary use of non-downloadable computer software for medical and scientific research in connection with primary template-directed amplification for use in connection with single cells and ultra-low DNA input samples
    29. Providing temporary use of non-downloadable computer software for medical and scientific research for the purpose of elevating single cell genome variants for the purpose of genome amplification
    30. Providing temporary use of non-downloadable computer software for DNA analysis and sequencing services for scientific, medical, and research purposes
    31. Providing temporary use of non-downloadable computer software for research, development and consultancy in the field of genomics
    32. Providing temporary use of non-downloadable computer software for compiling data for research purposes in the field of genomics
    33. Providing temporary use of non-downloadable computer software for providing medical research information in the field of genomics, gene therapy, cell therapy for medical purposes
    34. Providing temporary use of non-downloadable computer software for use in connection with medical testing, diagnosis, and treatment purposes
    35. Providing temporary use of non-downloadable computer software for use in connection with offering medical analysis services for diagnostic and treatment purposes provided by medical laboratories
    36. Providing temporary use of non-downloadable computer software for use in connection with medical diagnostic testing, monitoring, and reporting services
    37. Providing temporary use of non-downloadable computer software for medical analysis and diagnostic services in connection with the fields of oncology, cardiology, prenatal genetic testing (PGT), neurological genetic disorders, immunology, microbiome, toxicology, and bioprocessing
    38. Providing temporary use of non-downloadable computer software for medical analysis and diagnostic services in the field of gene therapy and cell therapy
    39. Providing temporary use of non-downloadable computer software for medical analysis and diagnostic services in the fields of genetics, genomics, proteomics, transcriptomics, epigenomics, metabolomics, meta-genomics, meta-transcriptomics, and microbiomics.
  • The mark was filed in class 44 with following description of goods:
    1. Medical testing for diagnostic or treatment purposes
    2. Medical analysis services for diagnostic and treatment purposes provided by medical laboratories
    3. Medical diagnostic testing, monitoring and reporting services
    4. Medical analysis and diagnostic services in connection with the fields of oncology, cardiology, prenatal genetic testing (PGT), neurological genetic disorders, immunology, microbiome, toxicology, and bioprocessing
    5. Medical analysis and diagnostic services in the field of gene therapy and cell therapy
    6. Medical analysis and diagnostic services in the fields of genetics, genomics, proteomics, transcriptomics, epigenomics, metabolomics, meta-genomics, meta-transcriptomics, and microbiomics.