The present invention presents methods for gene expression monitoring that utilize microelectronic arrays to drive the transport and hybridization of nucleic acids. Procedures are described for generating mRNA expression samples for use in these methods from populations of cells, tissues, or other biological source materials, that may differ in their physiological and/or pathological state. Provided in the invention are methods for generating a reusable nucleic acid transcript library from mRNA in a sample of biological material. In order to improve gene expression monitoring on the microelectronic arrays, the transcripts are amplified to produce sample nucleic acid amplicons of a defined length. Because multiple sample amplicons may be selectively hybridized to controlled sites in the electronic array, the gene expression profiles of the polynucleotide populations from different sources can be directly compared in an array format using electronic hybridization methodologies. Also provided in the invention are methods for detecting the level of sample amplicons using electronically assisted primer extension detection, and utilizing individual test site hybridization controls.
Methods For Determination Of Single Nucleic Acid Polymorphisms Using Bioelectronic Microchip
Michael I. Nerenberg - La Jolla CA David M. Canter - San Diego CA Ray R. Radtkey - San Diego CA Ling Wang - San Diego CA James P. Oconnell - Solana Beach CA Ronald G. Sosnowski - Coronado CA
Assignee:
Nanogen, Inc. - San Diego CA
International Classification:
C12Q 168
US Classification:
435 6, 422 50, 422 681
Abstract:
Methods are provided for the analysis and determination of the nature of single nucleic acid polymorphisms (SNPs) in a genetic target. In one method of this invention, the nature of the SNPs in the genetic target is determined by the steps of providing a plurality of hybridization complexes arrayed on a plurality of test sites on an electronically bioactive microchip, where the hybridization complex includes at least a nucleic acid target containing a SNP, a stabilizer probe having a sequence complementary to the target sequence and/or reporter probe, and a reporter probe having a selected sequence complementary to either the stabilizer or the same target sequence strand wherein a selected sequence of the reporter includes either a wild type nucleotide or a nucleotide corresponding to the SNP of the target. In accordance with the invention, the stabilizer, reporter and target amplicons are hybridized using electronic assistance of the microchip system such that base-stacking energies are utilized in discerning among other identifying indicators, the presence of wild type or polymorphism sequence. Applications include disease diagnostics, such as for the identification of polymorphisms in structural genes, regulatory regions, antibiotic or chemotherapeutic resistance conferring regions, or for SNPs associated with speciation or used for determination of genetic linkage.
Quantitative Analysis Methods On Active Electronic Microarrays
The present invention presents techniques useful in methods for gene expression monitoring, and other nucleic acid hybridization assays, that utilize microelectronic arrays to drive the transport and hybridization of nucleic acids. Particularly, methods for normalizing the signals of individual microlocations by the use of an internal control sequence probe are provided. These methods are particularly useful for hybridization assays in which a quantitative comparison of the hybridization of several different sequences at a plurality of microlocations is desired, such as in gene expression analyses.
Architecture Of Ballast With Integrated Rf Interface
Ihor Terence Wacyk - Briarcliff Manor NY Ling Wang - Millwood NY Johannes Hendrik Wessels - Mierlo, NL
Assignee:
Koninklijke Philips Eletronics N.V. - Eindhoven
International Classification:
G05F 100
US Classification:
315291, 315DIG 4, 315149, 315294
Abstract:
The invention is a new architecture for a high frequency (HF) ballast with wireless communication interface. The new architecture integrates the RF wireless interface into the ballast. A user control transmits an RF control signal to a second antenna at the ballast site which provides the RF signal to the ballast which activates the fluorescent lamp. The ballast includes a transceiver/receiver, a communication decoder, a power control stage and a power stage. The transceiver/receiver receives the RF signal and communicates it to the communication decoder which acts as an interface to the power stage control. The power stage control controls the power stage that activates the fluorescent lamp. The communication decoder, power control stage, power stage and transceiver/receiver are located within the ballast enclosure which is an important part of the invention. If the power stage control is digital it may be combined with the communication decoder into one microprocessor or digital controller such as an ASIC.
Method And System For Assigning And Binding A Network Address Of A Ballast
Ling Wang - Ossining NY Ihor Wacyk - Briarcliff Manor NY
Assignee:
Koninklijke Philips Electronics N.V. - Eindhoven
International Classification:
G08C 1900
US Classification:
34082552, 340 35
Abstract:
A system for implementing a method for initializing and binding ballasts is disclosed. The system comprises a remote control having a master controller and the ballasts each having a slave controller. The master controller and the slave controllers are operated to implement routines whereby the master controller generates a clock sequence of a plurality of clock cycles, and the slave controllers randomly generate addresses and direct a transmission of signals indicative of the generated random addresses to the master controller during corresponding clock cycles. In response thereto, the master controller assigns network addresses corresponding to the random addresses as indicated by the corresponding clock cycles. The master controller and the slave controllers are further operated to implement routines for verifying the assigned network addresses and routines for binding each network address to a command of the remote control.
Initialization Of Wireless-Controlled Lighting Systems
A method of initializing system components of a wireless-controlled lighting system. The system components include a remote control and a plurality of lighting units which communicate with a control master for the system via commonly-received radio communications. In order to become part of the system, each component transmits a respective request for initialization. A local control master for the system responds to each request, in turn, by allocating and transmitting a unique ID code for the requesting component. It then transmits a verify command to the requesting component which, if it has received the ID code, signals the user affirmatively.
System And Method For Lighting Control Network Recovery From Master Failure
Ling Wang - Millwood NY, US Demetri J. Giannopoulos - Norwalk CT, US
Assignee:
Koninklijke Philips Electronics N.V. - Eindhoven
International Classification:
H05B 41/00 H02J 3/14
US Classification:
315317, 315321, 307 40
Abstract:
The present invention provides a master-slave architecture for a radio frequency RF networked lighting control system having all slave elements (ballasts) configured as backups for a network master control unit. In the system and method of the present invention a slave element can become the network master network unit without reconfiguring the network and without any human intervention. Similarly, both a master and one or more slave elements may recover from a temporary outage without necessitating reconfiguration of the network and without any human intervention.
Methods For Determination Of Single Nucleic Acid Polymorphisms Using A Bioelectronic Microchip
Ronald G. Sosnowski - Coronado CA, US Michael I. Nerenberg - La Jolla CA, US David M. Canter - San Diego CA, US Ray R. Radtkey - San Diego CA, US Ling Wang - San Diego CA, US James P. O'Connell - Solana Beach CA, US
This application includes methods for detecting single nucleotide polymorphisms (SNPs) in a sample using an electronically addressable microchip having a plurality of test sites. A sample nucleic acid is electronically biased, concentrated at, and immobilized to a test site on the microchip. A mixture comprising a first labeled probe and a second labeled probe is electronically hybridized to the sample nucleic acid to form first or second hybridized complexes. The first labeled probe is perfectly complementary to the first sample nucleic acid and the second labeled probe is complementary to the sample nucleic acid and contains a nucleotide that forms a mismatch with the nucleotide at the site of the polymorphism. The first or second hybridized complexes are detected by determining a signal intensity of the label of the first or second probe.
Name / Title
Company / Classification
Phones & Addresses
Ling Wang President
Gentarget Inc. Commercial Physical and Biological Research
9865 Mesa Rim Rd Ste 207, San Diego, CA 92121
Ling Wang Graphic Designer
Jordache, Limited Women's, Children's, and Infants' Clothing an...
Deutsche Bank Group Jersey City, NJ Jan 2008 to Jun 2011 Service Validation & Testing Americas LeadDeutsche Bank Group Jersey City, NJ 2008 to 2009 Business Process AnalystMycroft Inc New York, NY 2005 to 2007 Business Systems Analyst/ITIL SME/Project CoordinatorTideway Systems Inc New York, NY 2004 to 2005 Office Manager/Marketing CoordinatorAppilog, Inc New York, NY 2002 to 2004 Office Manager/Inside Sales AssociateCreative Media, LLP New York, NY 1999 to 2000 Information Systems ManagerEdelman Public Relations Worldwide New York, NY 1998 to 1999 Technical SpecialistResearch Institute of America New York, NY 1997 to 1998 Electronic Product Production Operator
Education:
State University of New York Buffalo Buffalo, NY 1996 Bachelor of Arts in Psychology
RALINK TECHNOLOGY CORPORATION, A MEDIATEK COMPANY Cupertino, CA 2008 to 2010 Strategic Marketing/Business Development ManagerUBICOM Inc Sunnyvale, CA 2008 to 2008 Senior Product Marketing ManagerVENTURI WIRELESS Sunnyvale, CA 2006 to 2007 Director, Program Management, Product Management GroupPHILIPS ELECTRONICS NORTH AMERICA Briarcliff Manor, NY Dec 1998 to Sep 2006 Acting Product Manager / Senior Member of Technical Staff (2002 ~ 2006); Member of Technical Staff (1998 ~ 2002)
Education:
KELLOGG SCHOOL OF MANAGEMENT, NORTHWESTERN UNIVERSITY Chicago, IL 2006 Master of Business Administration in Management & StrategyRENSSELAER POLYTECHNIC INSTITUTE Troy, NY 1998 Master of Science in Electrical EngineeringTSINGHUA UNIVERSITY 1995 Bachelor of Science in Engineering Physics
Skills:
Strategic marketing, Strategic planning, business development, partnership development, product management
eriodically throughout Chinese history, rulers have sought to centralize control and isolate China from the outside. As Fei-Ling Wang of the Georgia Institute of Technology pointed out in The China Order: Centralia, World Empire, and the Nature of Chinese Power, such attempts result in disaster for China.
Date: Jul 15, 2022
Category: Business
Source: Google
Chinese COVID-19 Vaccine Phase 2 Trial Results: Safe and Induces an Immune Response
unogenicity and safety of a recombinant adenovirus type-5-vectored COVID-19 vaccine in healthy adults aged 18 years or older: a randomised, double-blind, placebo-controlled, phase 2 trial by Feng-Cai Zhu, Xu-Hua Guan, Yu-Hua Li, Jian-Ying Huang, Tao Jiang, Li-Hua Hou, Jing-Xin Li, Bei-Fang Yang, Ling Wang, We