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Nathan Hillson Phones & Addresses

  • Kensington, CA
  • 555 Bartlett St APT 304, San Francisco, CA 94110
  • 915 Camino Ranchitos NW, Albuquerque, NM 87114 (505) 898-0747
  • Palo Alto, CA
  • Cambridge, MA
  • Jamaica Plain, MA
  • Somerville, MA
  • Houston, TX

Work

Company: Joint genome institute Sep 2012 Address: Walnut Creek, CA Position: Group lead

Education

Degree: PhD School / High School: Harvard Medical School 1999 to 2004 Specialities: BioPhysics

Skills

Molecular Biology • Bioinformatics • Biochemistry • Synthetic Biology • Biotechnology • Computational Biology • Life Sciences • Biophysics • Genetics • Microscopy • Dna • Pcr • Protein Purification • Lifesciences • Software Design • Cell • Protein Expression • Protein Engineering • Assay Development • Cell Biology • Biofuels • Gene Synthesis • Metabolic Engineering • Software Project Management • Software Development

Languages

English

Industries

Biotechnology

Resumes

Resumes

Nathan Hillson Photo 1

Director Of Synthetic Biology Informatics

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Location:
555 Bartlett St, San Francisco, CA 94110
Industry:
Biotechnology
Work:
Joint Genome Institute - Walnut Creek, CA since Sep 2012
Group Lead

TeselaGen Biotechnology - San Francisco Bay Area since Sep 2011
Founder and Chief Scientific Officer

Joint BioEnergy Institute since Jun 2009
Director of Synthetic Biology

Lawrence Berkeley National Laboratory since Jun 2009
Biochemist Staff Scientist

Department of Developmental Biology, Stanford University School of Medicine 2005 - 2009
Postdoctoral Research Fellow
Education:
Harvard Medical School 1999 - 2004
PhD, BioPhysics
Rice University 1995 - 1999
B.A., Physics/CAAM
Albuquerque Academy 1988 - 1995
Skills:
Molecular Biology
Bioinformatics
Biochemistry
Synthetic Biology
Biotechnology
Computational Biology
Life Sciences
Biophysics
Genetics
Microscopy
Dna
Pcr
Protein Purification
Lifesciences
Software Design
Cell
Protein Expression
Protein Engineering
Assay Development
Cell Biology
Biofuels
Gene Synthesis
Metabolic Engineering
Software Project Management
Software Development
Languages:
English

Publications

Us Patents

Microfluidic Platform For Synthetic Biology Applications

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US Patent:
20120258487, Oct 11, 2012
Filed:
Apr 2, 2012
Appl. No.:
13/437727
Inventors:
Chieh Chang - San Jose CA, US
Rajiv Bharadwaj - Emeryville CA, US
Anup K. Singh - Danville CA, US
Aarthi Chandrasekaran - San Jose CA, US
Nathan J. Hillson - San Francisco CA, US
Assignee:
THE REGENTS OF THE UNIVERSITY OF CALIFORNIA - Oakland CA
SANDIA CORPORATION - Livermore CA
International Classification:
C12P 19/34
C12N 15/63
C12M 1/00
C12N 15/82
C12Q 1/04
C12M 1/40
C12N 11/00
C12N 15/85
US Classification:
435 34, 435174, 435 915, 435 9152, 435 9141, 435 912, 435440, 435471, 435455, 435468, 4352891
Abstract:
This invention provides methods and compositions for assembling biological constructs (e.g., plasmids, transformed cells, etc.). In certain embodiments the methods involve encapsulating separate components of said biological construct each in a fluid droplet confined in a fluid channel; optionally mixing droplets from different fluid channels to for a sequenced order of droplets carrying different components of said biological construct in a channel or chamber; and optionally combining two or more droplets each containing different components of said biological construct to permit said components to react with each other in one or more reactions contributing to the assembly of said biological construct.

Scar-Less Multi-Part Dna Assembly Design Automation

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US Patent:
20120259607, Oct 11, 2012
Filed:
Feb 1, 2012
Appl. No.:
13/364285
Inventors:
Nathan J. Hillson - San Francisco CA, US
Assignee:
THE REGENTS OF THE UNIVERSITY OF CALIFORNIA - OAKLAND CA
International Classification:
G06G 7/60
US Classification:
703 11
Abstract:
The present invention provides a method of a method of designing an implementation of a DNA assembly. In an exemplary embodiment, the method includes (1) receiving a list of DNA sequence fragments to be assembled together and an order in which to assemble the DNA sequence fragments. (2) designing DNA oligonucleotides (oligos) for each of the DNA sequence fragments, and (3) creating a plan for adding flanking homology sequences to each of the DNA oligos. In an exemplary embodiment, the method includes (1) receiving a list of DNA sequence fragments to be assembled together and an order in which to assemble the DNA sequence fragments, (2) designing DNA oligonucleotides (oligos) for each of the DNA sequence fragments, and (3) creating a plan for adding optimized overhang sequences to each of the DNA oligos.

Heavy Metal Biosensor

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US Patent:
20110117590, May 19, 2011
Filed:
Feb 6, 2008
Appl. No.:
12/526312
Inventors:
Nathan J. Hillson - San Francisco CA, US
Lucille Shapiro - Stanford CA, US
Ping Hu - San Ramon CA, US
Gary L. Andersen - Berkeley CA, US
International Classification:
C12Q 1/02
C12N 1/21
US Classification:
435 29, 4352523
Abstract:
Compositions and methods are provided for detection of certain heavy metals using bacterial whole cell biosensors.

Scar-Less Multi-Part Dna Assembly Design Automation

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US Patent:
20200005891, Jan 2, 2020
Filed:
Jun 7, 2019
Appl. No.:
16/435406
Inventors:
- Oakland CA, US
Nathan J. Hillson - San Francisco CA, US
International Classification:
G16B 15/00
G16B 20/00
G16B 25/00
G16B 30/00
Abstract:
The present invention provides a method of a method of designing an implementation of a DNA assembly. In an exemplary embodiment, the method includes (1) receiving a list of DNA sequence fragments to be assembled together and an order in which to assemble the DNA sequence fragments, (2) designing DNA oligonucleotides (oligos) for each of the DNA sequence fragments, and (3) creating a plan for adding flanking homology sequences to each of the DNA oligos. In an exemplary embodiment, the method includes (1) receiving a list of DNA sequence fragments to be assembled together and an order in which to assemble the DNA sequence fragments, (2) designing DNA oligonucleotides (oligos) for each of the DNA sequence fragments, and (3) creating a plan for adding optimized overhang sequences to each of the DNA oligos.

Scar-Less Multi-Part Dna Assembly Design Automation

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US Patent:
20160378913, Dec 29, 2016
Filed:
May 5, 2016
Appl. No.:
15/147764
Inventors:
- Oakland CA, US
Nathan J. Hillson - San Francisco CA, US
International Classification:
G06F 19/16
G06F 19/18
G06F 19/20
G06F 19/22
Abstract:
The present invention provides a method of a method of designing an implementation of a DNA assembly. In an exemplary embodiment, the method includes (1) receiving a list of DNA sequence fragments to be assembled together and an order in which to assemble the DNA sequence fragments, (2) designing DNA oligonucleotides (oligos) for each of the DNA sequence fragments, and (3) creating a plan for adding flanking homology sequences to each of the DNA oligos. In an exemplary embodiment, the method includes (1) receiving a list of DNA sequence fragments to be assembled together and an order in which to assemble the DNA sequence fragments, (2) designing DNA oligonucleotides (oligos) for each of the DNA sequence fragments, and (3) creating a plan for adding optimized overhang sequences to each of the DNA oligos.
Nathan J Hillson from Kensington, CA, age ~47 Get Report