IP Library Granted Patent US 7,424,371
Granted Patent B2
US 7,424,371 · App. 11/018,515 · Granted Sep 9, 2008

Nucleic acid analysis

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Quick Facts
Patent No.
US 7,424,371
App. No.
11/018,515
Granted
Sep 9, 2008
Kind
B2
Abstract

A sample nucleic acid sequence is compared against a database to find a matching sequence. In one embodiment, this comparison is accomplished with a table look-up approach that involves using sequences with collapsed homopolymer regions.

Claims (11)

1. A method of comparing nucleic acid sequences, wherein all of the following steps are performed on a computer, the method comprising:

providing a nucleic acid sequence obtained from a sample and including at least one homopolymer region;

collapsing each of the homopolymer regions to a single nucleotide to form a representative sample sequence without homopolymer regions; and

comparing the representative sample sequence to at least one of a plurality of collapsed reference nucleic acid sequences without homopolymer regions to determine whether the representative sample sequence matches one of the plurality of reference nucleic acid sequences; and

providing results of the comparing step to a user.

2. The method of claim 1 , wherein the steps of collapsing and comparing include the use of indexes and a binary search to determine whether the representative sample sequence matches one of the plurality of reference nucleic acid sequences.

3. The method of claim 1 , wherein each of the plurality of reference nucleic acid sequences comprises a cDNA or RNA sequence.

4. A method of matching nucleic acid sequences, wherein all of the following steps are performed on a computer, the method comprising:

collapsing each homopolymer region of a patient nucleic acid sequence to a single nucleotide to form a representative sample sequence; and

determining whether the representative sample sequence matches a member of a database of reference nucleic acid sequences without homopolymer regions, at least one of the reference nucleic acid sequences created by collapsing at least one homopolymer region to a single nucleotide, at least some of the reference nucleic acid sequences being indicative of a diagnosis or prognosis; providing results of the determining step to a user.

5. The method of claim 4 , wherein the steps of collapsing and determining include the use of indexes and a binary search to determine whether the representative sample sequence matches a member of the database of reference nucleic acid sequences.

Assignments (8)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 28, 2013
From: HELICOS BIOSCIENCES CORPORATION
To: FLUIDIGM CORPORATION
Reel/Frame 030714/0546 →
LICENSE Recorded Jun 28, 2013
From: FLUIDIGM CORPORATION
To: PACIFIC BIOSCIENCES OF CALIFORNIA, INC.
Reel/Frame 030714/0598 →
LICENSE Recorded Jun 28, 2013
From: FLUIDIGM CORPORATION
To: SEQLL, LLC
Reel/Frame 030714/0633 →
LICENSE Recorded Jun 28, 2013
From: FLUIDIGM CORPORATION
To: COMPLETE GENOMICS, INC.
Reel/Frame 030714/0686 →
LICENSE Recorded Jun 28, 2013
From: FLUIDIGM CORPORATION
To: ILLUMINA, INC.
Reel/Frame 030714/0783 →
RELEASE OF SECURITY INTEREST Recorded Jan 18, 2012
From: GENERAL ELECTRIC CAPITAL CORPORATION
To: HELICOS BIOSCIENCES CORPORATION
Reel/Frame 027549/0565 →
SECURITY AGREEMENT Recorded Nov 22, 2010
From: HELICOS BIOSCIENCES CORPORATION
To: GENERAL ELECTRIC CAPITAL CORPORATION
Reel/Frame 025388/0347 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 17, 2005
From: KAMENTSKY, LEE D.
To: HELICOS BIOSCIENCES CORPORATION
Reel/Frame 015735/0022 →