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Khai T Luong

from San Francisco, CA
Age ~63

Khai Luong Phones & Addresses

  • 762 7Th Ave, San Francisco, CA 94118 (415) 752-5624
  • Boston, MA
  • Richmond, CA

Resumes

Resumes

Khai Luong Photo 1

Director Of Bioinformatics

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Location:
3815 Laguna Ave, Oakland, CA 94602
Industry:
Biotechnology
Work:
Roche Sequencing Solutions
Director of Bioinformatics

Pacific Biosciences Mar 2011 - Dec 2014
Staff Scientist: Next Generation Applications and Technologies

Pacific Biosciences Apr 2007 - Mar 2011
Senior Scientist: Single Molecule Sequencing

Life Technologies Jan 2006 - Apr 2007
Senior Scientist

Sandia National Laboratories Mar 2002 - Jan 2006
Scientist
Education:
Uc San Diego 1996 - 2001
Doctorates, Doctor of Philosophy, Chemistry
Skills:
Bioinformatics
Genomics
Dna
Biotechnology
Dna Sequencing
Fluorescence
Sequencing
Computational Biology
R
Assay Development
Sequence Analysis
Microscopy
Epigenetics
R&D
Optics
Product Development
Assay Dev
Life Sciences
Languages:
English
Khai Luong Photo 2

Customer Success

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Location:
San Francisco, CA
Industry:
Financial Services
Work:
Bolt
Customer Success

Oh My Green Oct 2016 - Mar 2018
Head of Happiness

Practice Fusion Sep 2010 - Aug 2014
Senior Account Manager

Courserank Inc. Jun 2010 - Sep 2010
Sales Manager
Education:
Stanford University 2006 - 2010
Bachelors, Bachelor of Science, Biology, Physics
Skills:
Product Management
Saas
Salesforce.com
Start Ups
Strategy
Business Development
Strategic Partnerships
Data Analysis
Cloud Computing
Project Management
Khai Luong Photo 3

Khai Luong

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Khai Luong Photo 4

Khai Luong

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Publications

Us Patents

Intermediates And Methods For Forming Passivated Surfaces On Oxide Layers And Articles Produced Thereby

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US Patent:
20080176761, Jul 24, 2008
Filed:
Nov 21, 2007
Appl. No.:
11/943851
Inventors:
Steven M. Menchen - Fremont CA, US
Christina E. Inman - San Mateo CA, US
Meng Taing - Hayward CA, US
Khai Luong - Oakland CA, US
Handong Li - San Jose CA, US
Assignee:
APPLERA CORPORATION, APPLIED BIOSYSTEMS GROUP - Foster City CA
International Classification:
C40B 50/14
C40B 40/00
C07F 9/09
C07F 9/02
C40B 50/18
US Classification:
506 13, 506 32, 558 70, 506 42, 562 8
Abstract:
Intermediates and methods for forming passivated surfaces on oxide layers and articles produced thereby are described. Hydroxyl or hydroxide groups on the oxide surfaces are reacted with a metal reagent of the formula Y(L-Pol), where Y is a transition metal, magnesium or aluminum, L is oxygen, sulfur, selenium or an amine, and “Pol” represents a passivating agent such as a polyethylene glycol, a hydrocarbon, or a fluorocarbon. The resulting modified surface can be further reacted with a passivating agent having a phosphate functional group or a polyvalent reagent comprising a passivating moiety and a plurality of functional groups that are reactive with or that form complexes with Y. The passivating agent can also include a functional group such as biotin to provide surfaces with a desired functionality. The passivated surfaces exhibit minimal binding to bio-molecules and can be used in single-molecule detection schemes.

Methods And Systems For Analysis Of Fluorescent Reactions With Modulated Excitation

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US Patent:
20090181396, Jul 16, 2009
Filed:
Jan 9, 2009
Appl. No.:
12/351173
Inventors:
Khai Luong - Oakland CA, US
Paul Lundquist - San Jose CA, US
Ravi Dalal - Menlo Park CA, US
John Lyle - Redwood Shores CA, US
Stephen Turner - Menlo Park CA, US
Assignee:
Pacific Biosciences of California, Inc. - Menlo Park CA
International Classification:
C12Q 1/68
G01N 21/76
C12M 1/34
US Classification:
435 6, 422 8208, 436172, 4352872
Abstract:
Methods, systems and their components for monitoring fluorescent signals and particularly transient fluorescent signals from reaction mixtures of interest, which methods and systems employ modulated excitation light sources to reduce impacts of excessive illumination on the reaction components or the data obtained therefrom.

Intermediates And Methods For Forming Passivated Surfaces On Oxide Layers And Articles Produced Thereby

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US Patent:
20110159305, Jun 30, 2011
Filed:
Mar 10, 2011
Appl. No.:
13/044759
Inventors:
Steven M. MENCHEN - Fremont CA, US
Christina E. Inman - San Mateo CA, US
Meng Taing - Hayward CA, US
Khai Luong - Oakland CA, US
Handong Li - San Jose CA, US
Assignee:
APPLIED BIOSYSTEMS, LLC - Carlsbad CA
International Classification:
B32B 15/00
US Classification:
428457
Abstract:
Intermediates and methods for forming passivated surfaces on oxide layers and articles produced thereby are described. Hydroxyl or hydroxide groups on the oxide surfaces are reacted with a metal reagent of the formula Y(L-Pol), where Y is a transition metal, magnesium or aluminum, L is oxygen, sulfur, selenium or an amine, and “Pol” represents a passivating agent such as a polyethylene glycol, a hydrocarbon, or a fluorocarbon. The resulting modified surface can be further reacted with a passivating agent having a phosphate functional group or a polyvalent reagent comprising a passivating moiety and a plurality of functional groups that are reactive with or that form complexes with Y. The passivating agent can also include a functional group such as biotin to provide surfaces with a desired functionality. The passivated surfaces exhibit minimal binding to bio-molecules and can be used in single-molecule detection schemes.

Systems And Methods For Cell Of Origin Determination From Variant Calling Data

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US Patent:
20220259667, Aug 18, 2022
Filed:
Jul 20, 2020
Appl. No.:
17/597760
Inventors:
- Pleasanton CA, US
Hai Lin - San Bruno CA, US
Alexander Lovejoy - Newark CA, US
Khai Luong - Oakland CA, US
Ehsan Tabari - San Francisco CA, US
International Classification:
C12Q 1/6886
G16B 20/20
G16B 40/20
Abstract:
The present invention relates generally to classification of biological samples, and more specifically to cell of original classification. In particular, some embodiments of the invention relate to diffuse large B cell lymphoma cell of origin classification using machine learning models. The machine learning models can be based on decision trees such as a random forest algorithm or a gradient boosted decision tree. Features for the models can be determined through analysis of variant data from plasma or blood samples from a plurality of subjects with the disease.

Direct Variant Phasing In Long Reads To Detect Quasispecies

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US Patent:
20200211675, Jul 2, 2020
Filed:
Sep 12, 2018
Appl. No.:
16/646962
Inventors:
- Pleasanton CA, US
Khai LUONG - Oakland CA, US
Garima KUSHWAHA - San Francisco CA, US
International Classification:
G16B 30/00
C12Q 1/6869
G16B 20/20
Abstract:
Described herein are methods for identifying quasispecies of genomes by clustering sequence reads for samples including the genomes based on the similarities of the sequence reads.

Compositions And Methods For Enrichment Of Nucleic Acids

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US Patent:
20200109396, Apr 9, 2020
Filed:
Aug 28, 2019
Appl. No.:
16/553915
Inventors:
- Menlo Park CA, US
Igor Vilfan - East Palo Alto CA, US
Khai Luong - San Francisco CA, US
International Classification:
C12N 15/10
C12Q 1/6806
C12Q 1/6869
C40B 50/06
Abstract:
Methods are provided for reducing the complexity of a population of nucleic acids prior to performing an analysis of the nucleic acids, e.g., sequence analysis. The methods result in a subset of the initial population enriched for a target region, which is typically located within one or more target fragments. The methods are particularly useful for analyzing populations having a high degree of complexity, e.g., chromosomal-derived DNA, whole genomic DNA, or mRNA populations.

Compositions And Methods For Enrichment Of Nucleic Acids

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US Patent:
20160208241, Jul 21, 2016
Filed:
Jan 14, 2016
Appl. No.:
14/995646
Inventors:
- Menlo Park CA, US
Igor Drasko Vilfan - East Palo Alto CA, US
Khai Luong - San Francisco CA, US
International Classification:
C12N 15/10
C12Q 1/68
Abstract:
Methods are provided for reducing the complexity of a population of nucleic acids prior to performing an analysis of the nucleic acids, e.g., sequence analysis. The methods result in a subset of the initial population enriched for a target region, which is typically located within one or more target fragments. The methods are particularly useful for analyzing populations having a high degree of complexity, e.g., chromosomal-derived DNA, whole genomic DNA, or mRNA populations.
Khai T Luong from San Francisco, CA, age ~63 Get Report