Trademark: BIOSKRYB GENOMICS 2193920
Word
BIOSKRYB GENOMICS
ID
2193920
Trademark Type
Word
Status
Registered: Registered/protected
Application Date
13 July 2021
Registration Date
13 July 2021
Renewal Date
13 July 2031

Service
Davies Collison Cave Pty Ltd

Goods and Services:
Class 1:
Assays and reagents for use in genetic research; diagnostic reagents for scientific, and research use; reagents and reagent kits; 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; 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 research purposes; reagents and containers of reagents, namely, reagents for use in the amplification and recovery of genomic material, including genomic material from single cells; chemical substances and products for use in genomic research; biochemicals, namely, biological reagents for use in whole genome amplification to detect genetic variants in each cell; laboratory chemicals, namely, an antibody reagent used for genomic research; chemical kits for diagnostic purposes for laboratory and research use; 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 scientific research purposes; diagnostic kits comprised of reagents and assays for detecting, testing, analyzing, and sequencing genes, nucleic acids, and biological molecules; kits containing reagents for scientific purposes comprising paramagnetic beads for the processing, purification, and cleanup of samples containing genomic material, including material from single cells; kits containing assays, reagents, and chemical substances and products for use in genomic research; kits containing biochemicals, namely, biological reagents for use in whole genome amplification to detect genetic variants in each cell; kits containing laboratory chemicals, namely, an antibody reagent used for genomic research
Class 5:
Diagnostic for medical use; 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 purposes; chemical kits for diagnostic purposes for medical use; diagnostic reagents for clinical or medical laboratory use; diagnostic kits comprising of reagents for medical use; 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 purposes; kits comprising reagents for medical use in relation to amplification and recovery of genomic material, including genomic material from single cells; medical test kits comprised of biological reagents for use in whole genome amplification to detect genetic variants in cells; kits containing reagents for medical use comprising paramagnetic beads for the processing, purification, and cleanup of samples containing genomic material, including material from single cells; 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 purposes; kits comprising reagents for medical use in relation to amplification and recovery of genomic material, including genomic material from single cells; medical test kits comprised of biological reagents for use in whole genome amplification to detect genetic variants in cells; kits containing reagents for medical use comprising paramagnetic beads for the processing, purification, and cleanup of samples containing genomic material, including material from single cells
Class 9:
Downloadable computer software including 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; 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; 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; 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; 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; downloadable computer software for genomic analysis and sequencing for scientific, medical, and research purposes; downloadable computer software for medical and scientific research in the fields of genetics, genomics, proteomics, transcriptomics, epigenomics, metabolomics, meta-genomics, meta-transcriptomics, and microbiomics; downloadable computer software for nucleic acid and ribonucleic acid analysis for medical and scientific research purposes; 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; 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; downloadable computer software for medical and scientific research in connection with genome amplification to detect genetic variants in cells; downloadable computer software for medical and scientific research in connection with measuring genetic diversity in single cells; 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; downloadable computer software for medical and scientific research for the purpose of elevating single cell genome variants for the purpose of genome amplification; downloadable computer software for DNA analysis and sequencing services for scientific, medical, and research purposes; downloadable computer software for research, development and consultancy in the field of genomics; downloadable computer software for compiling data for research purposes in the field of genomics; downloadable computer software for providing medical research information in the field of genomics, gene therapy, cell therapy for medical purposes; downloadable computer software for use in connection with medical testing, diagnosis, and treatment purposes; downloadable computer software for use in connection with offering medical analysis services for diagnostic and treatment purposes provided by medical laboratories; downloadable computer software for use in connection with medical diagnostic testing, monitoring, and reporting services; 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; downloadable computer software for medical analysis and diagnostic services in the field of gene therapy and cell therapy; 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; diagnostic kits being diagnostic apparatus comprising of reagents for scientific use; scientific and laboratory apparatus and instruments for the amplification and recovery of genomic material, including genomic material from single cells; scientific and 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; kits comprising laboratory apparatus or instrument for the amplification and recovery of genomic material, including genomic material from single cells; kits containing medical and scientific apparatus for use in genetic research; kits comprising of apparatus for diagnostic purposes for laboratory or scientific research use; kits containing a diagnostic scientific or laboratory apparatus or instrument, namely, kits comprising multi-well plates, and magnetic plates comprising paramagnetic beads for the processing, purification, and cleanup of samples containing genomic material, including material from single cells
Class 42:
Genomic analysis and sequencing services for scientific, medical, and research purposes; medical and scientific research in the fields of genetics, genomics, proteomics, transcriptomics, epigenomics, metabolomics, meta-genomics, meta-transcriptomics, and microbiomics; nucleic acid and ribonucleic acid analysis services for medical and scientific research purposes; providing medical and scientific research information in the fields of genetics, genomics, proteomics, transcriptomics, epigenomics, metabolomics, meta-genomics, meta-transcriptomics, and microbiomics; 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; medical and scientific research in connection with genome amplification to detect genetic variants in cells; medical and scientific research in connection with measuring genetic diversity in single cells; medical and scientific research in connection with primary template-directed amplification for use in connection with single cells and ultra-low DNA input samples; medical and scientific research for the purpose of elevating single cell genome variants for the purpose of genome amplification; DNA analysis and sequencing services for scientific, medical, and research purposes; research, development and consultancy in the field of genomics; medical research, namely, compiling data for research purposes in the field of genomics; providing medical research information in the field of genomics, gene therapy, cell therapy for medical purposes; 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; 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; 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; 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; 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; providing temporary use of non-downloadable computer software for genomic analysis and sequencing for scientific, medical, and research purposes; 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; providing temporary use of non-downloadable computer software for nucleic acid and ribonucleic acid analysis for medical and scientific research purposes; 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; 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; providing temporary use of non-downloadable computer software for medical and scientific research in connection with genome amplification to detect genetic variants in cells; providing temporary use of non-downloadable computer software for medical and scientific research in connection with measuring genetic diversity in single cells; 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; 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; providing temporary use of non-downloadable computer software for DNA analysis and sequencing services for scientific, medical, and research purposes; providing temporary use of non-downloadable computer software for research, development and consultancy in the field of genomics; providing temporary use of non-downloadable computer software for compiling data for research purposes in the field of genomics; 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; providing temporary use of non-downloadable computer software for use in connection with medical testing, diagnosis, and treatment purposes; 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; providing temporary use of non-downloadable computer software for use in connection with medical diagnostic testing, monitoring, and reporting services; 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; providing temporary use of non-downloadable computer software for medical analysis and diagnostic services in the field of gene therapy and cell therapy; 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