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GREEN CROSS GENOME CORP

Overview
  • Total Patents
    26
  • GoodIP Patent Rank
    61,952
  • Filing trend
    ⇩ 40.0%
About

GREEN CROSS GENOME CORP has a total of 26 patent applications. It decreased the IP activity by 40.0%. Its first patent ever was published in 2015. It filed its patents most often in Republic of Korea, WIPO (World Intellectual Property Organization) and Brazil. Its main competitors in its focus markets biotechnology, computer technology and measurement are VERINATA HEALTH INC, AGILENT TECH BELGIUM NV and EONE DIAGNOMICS GENOME CENTER CO LTD.

Patent filings in countries

World map showing GREEN CROSS GENOME CORPs patent filings in countries

Patent filings per year

Chart showing GREEN CROSS GENOME CORPs patent filings per year from 1900 to 2020

Focus industries

Top inventors

# Name Total Patents
#1 Cho Eun Hae 15
#2 Jeon Young Joo 14
#3 Lee Junnam 13
#4 Jang Ja Hyun 9
#5 Cho Eun-Hae 9
#6 Jeon Young-Joo 9
#7 Lee Taeheon 9
#8 Kim Ki Soo 8
#9 Jang Ja-Hyun 8
#10 Lee So Young 8

Latest patents

Publication Filing date Title
WO2021034034A1 Method for detecting chromosomal abnormality by using information about distance between nucleic acid fragments
KR20210021923A Method for detecting chromosomal abnormality using distance information between nucleic acid fragments
KR20200101106A Method for Prognosing Hepatic Cancer Patients Based on Circulating Cell Free DNA
KR20200034125A Markers for predicting concentration of statin in blood
KR20200012530A Method for Detecting Chromosomal Abnormalities Based on Whole Genome Sequencing and Uses thereof
KR20190085667A Circulating Tumor DNA Detection Method Using Sample comprising Cell free DNA and Uses thereof
WO2018016884A1 Composition for diagnosing congenital functional disorder, and use thereof
KR20180001442A Composition for detecting Birth Dysfunction and use thereof
KR20180001437A Composition for detecting Birth Dysfunction and use thereof
KR20180009999A Composition for detecting RASopathies and use thereof
KR20180010000A Composition for detecting Inherited Blood Coagulation Disorders and use thereof
KR20180009998A Composition for detecting Inborn Error of Metabolism and use thereof
KR101743211B1 Composition for detecting Birth Dysfunction and use thereof
KR101774996B1 Markers For Predicting Effect of Therapeutic Agent Against Hemophilia and Use Thereof
KR101686146B1 Copy Number Variation Determination Method Using Sample comprising Nucleic Acid Mixture
CN108475301A The method of copy number variation in sample for determining the mixture comprising nucleic acid