ACCURAGEN HOLDINGS LTD has a total of 47 patent applications. It decreased the IP activity by 80.0%. Its first patent ever was published in 2014. It filed its patents most often in United States, WIPO (World Intellectual Property Organization) and EPO (European Patent Office). Its main competitors in its focus markets biotechnology, computer technology and organic fine chemistry are HENDRIX GENETICS B V, GENESUPPORT SA and ZORAGEN BIOTECHNOLOGIES LLP.
# | Country | Total Patents | |
---|---|---|---|
#1 | United States | 12 | |
#2 | WIPO (World Intellectual Property Organization) | 8 | |
#3 | EPO (European Patent Office) | 7 | |
#4 | China | 6 | |
#5 | Canada | 3 | |
#6 | Israel | 3 | |
#7 | Singapore | 3 | |
#8 | Australia | 2 | |
#9 | Hong Kong | 1 | |
#10 | Republic of Korea | 1 | |
#11 | Mexico | 1 |
# | Industry | |
---|---|---|
#1 | Biotechnology | |
#2 | Computer technology | |
#3 | Organic fine chemistry | |
#4 | Environmental technology |
# | Name | Total Patents |
---|---|---|
#1 | Lin Shengrong | 38 |
#2 | Weng Li | 36 |
#3 | Sun Zhaohui | 18 |
#4 | Tang Ling Fung | 15 |
#5 | Faham Malek | 13 |
#6 | Zhao Grace Qizhi | 10 |
#7 | Tang Paul Ling-Fung | 7 |
#8 | Lu Yontao | 6 |
#9 | Wang Yingyu | 5 |
#10 | Lin Chia-Hui | 5 |
Publication | Filing date | Title |
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WO2020263978A1 | Methods and systems for disease detection | |
WO2020172566A1 | Methods and compositions for early cancer detection | |
WO2019241290A1 | Methods and compositions for forming ligation products | |
US2020010883A1 | Methods and compositions for enrichment of amplification products | |
US2019300949A1 | Compositions and methods comprising asymmetric barcoding | |
CN109844133A | Detect the composition and method of rare sequence variants | |
EP3475449A1 | Cell-free nucleic acid standards and uses thereof | |
WO2017201102A1 | Method of improved sequencing by strand identification | |
WO2017096322A1 | Methods and compositions for forming ligation products | |
CN108368545A | Method and composition for Enrichment Amplification product | |
EP3080298A1 | Methods for detecting rare sequence variants |