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COMPLETE GENOMICS INC

Overview
  • Total Patents
    252
  • GoodIP Patent Rank
    12,644
  • Filing trend
    ⇧ 15.0%
About

COMPLETE GENOMICS INC has a total of 252 patent applications. It increased the IP activity by 15.0%. Its first patent ever was published in 2004. 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, measurement and computer technology are VYSIS INC, OMNIOME INC and ROCHE SEQUENCING SOLUTIONS INC.

Patent filings per year

Chart showing COMPLETE GENOMICS INCs patent filings per year from 1900 to 2020

Top inventors

# Name Total Patents
#1 Drmanac Radoje 121
#2 Peters Brock A 41
#3 Staker Bryan P 34
#4 Drmanac Snezana 31
#5 Kermani Bahram Ghaffarzadeh 28
#6 Callow Matthew 25
#7 Callow Matthew J 23
#8 Alexeev Andrei 22
#9 Sparks Andrew 20
#10 Uhrich Craig E 19

Latest patents

Publication Filing date Title
US2019316190A1 Self-assembled single molecule arrays and uses thereof
WO2019060177A1 Wafer level sequencing flow cell fabrication
US2019070606A1 Injection molded microfluidic/fluidic cartridge integrated with silicon-based sensor
CN110551794A Method for treating RNA molecule, kit and complex
US2018245132A1 Methods for hybridization based hook ligation
MX2019008016A Stepwise sequencing by non-labeled reversible terminators or natural nucleotides.
TW201830004A Biosensors for biological or chemical analysis and methods of manufacturing the same
WO2018009677A1 Fast target enrichment by multiplexed relay pcr with modified bubble primers
CN109790196A Reversible closed nucleoside analog and application thereof
US2017240961A1 Affinity tag labeled nucleosides and uses
US2017022558A1 Integrated system for nucleic acid sequence and analysis
US2016117444A1 Methods for determining absolute genome-wide copy number variations of complex tumors
AU2015264833A1 Processing and analysis of complex nucleic acid sequence data
WO2016065248A1 Signal confinement sequencing (scs) and nucleotide analogues for signal confinement sequencing
US2015317433A1 Using doublet information in genome mapping and assembly
WO2015095066A1 Basecaller for dna sequencing using machine learning
CN109599148A That identifies the variation in genome determines phase and connection method
US2014323316A1 Multiple tagging of individual long DNA fragments
US2014085457A1 High-density devices with synchronous tracks for quad-cell based alignment correction
US2014152793A1 Techniques for scanned illumination