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公开(公告)号:US20230340570A1
公开(公告)日:2023-10-26
申请号:US18114091
申请日:2023-02-24
Applicant: Ultima Genomics, Inc.
Inventor: Daniel MAZUR , Kevin HEINEMANN , Theo NIKIFOROV , Robert ONO , Aklilu WORKU , Florian OBERSTRASS
IPC: C12Q1/6811
CPC classification number: C12Q1/6811
Abstract: The present disclosure provides methods, systems, compositions, and kits for reducing particle aggregation and improving sequencing quality. A method for processing particles may comprise the use of a first buffer solution or a second buffer solution. A method for processing particles may comprise the use of a single-strand binding moiety such as a single-strand binding protein.
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公开(公告)号:US20230313289A1
公开(公告)日:2023-10-05
申请号:US18076214
申请日:2022-12-06
Applicant: Ultima Genomics, Inc.
Inventor: Florian OBERSTRASS , Gilad ALMOGY
IPC: C12Q1/6869 , C12Q1/6874 , C12N15/10
CPC classification number: C12Q1/6869 , C12N15/1096 , C12Q1/6874 , C12Q2525/161 , C12Q2525/173 , C12Q2525/191 , C12Q2563/179 , C12Q2563/185 , C12Q2600/178 , C12Y207/07049
Abstract: Described herein are methods for determining a sequence of a region of interest from an mRNA molecule. Sequenced polynucleotides can include a barcode region, a homopolymer region (e.g., a poly-A region), and a target region associated with the mRNA molecule. According to some methods, the barcode region omits the same base present in the homopolymer region. According to some methods, extension of the primer used for sequencing is stalled within the homopolymer region. According to some methods, sequencing flow cycles and the different barcode regions of the polynucleotides configured are such that the primer is extended to the end of the barcode region across the plurality of polynucleotides before being extended into the homopolymer region. According to some methods, two primers or a cleavable primer is used to separately sequence the barcode region and the target region.
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公开(公告)号:US11732298B2
公开(公告)日:2023-08-22
申请号:US16416856
申请日:2019-05-20
Applicant: Ultima Genomics, Inc.
Inventor: Gilad Almogy , Kristopher Barbee , Nathan Beckett
IPC: C12Q1/6874 , C12Q1/6809 , C12Q1/6825 , B01J19/00 , B01L3/00 , G01N33/543 , C12Q1/6834
CPC classification number: C12Q1/6874 , B01J19/0046 , B01L3/50273 , B01L3/502715 , C12Q1/6809 , C12Q1/6825 , B01J2219/00536 , B01J2219/00596 , B01J2219/00605 , B01J2219/00689 , B01J2219/00702 , B01J2219/00722 , B01L3/5023 , B01L2200/026 , B01L2200/0647 , B01L2300/0654 , B01L2400/0409 , C12Q1/6834 , G01N33/54366 , C12Q1/6874 , C12Q2565/629 , C12Q1/6834 , C12Q2565/629
Abstract: Provided are methods for biological sample processing and analysis. A method can comprise providing a substrate configured to rotate. The substrate can comprise an array having immobilized thereto a biological analyte. A solution comprising a plurality of probes may be directed, via centrifugal force, across the substrate during rotation of the substrate, to couple at least one of the plurality of probes with the biological analyte. A detector can be configured to detect a signal from the at least one probe coupled to the biological analyte, thereby analyzing the biological analyte.
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公开(公告)号:US11578363B2
公开(公告)日:2023-02-14
申请号:US16925778
申请日:2020-07-10
Applicant: Ultima Genomics, Inc.
Inventor: Florian Oberstrass , Gilad Almogy
IPC: C12Q1/6869 , C12N15/10 , C12Q1/6874
Abstract: Described herein are methods for determining a sequence of a region of interest from an mRNA molecule. Sequenced polynucleotides can include a barcode region, a homopolymer region (e.g., a poly-A region), and a target region associated with the mRNA molecule. According to some methods, the barcode region omits the same base present in the homopolymer region. According to some methods, extension of the primer used for sequencing is stalled within the homopolymer region. According to some methods, sequencing flow cycles and the different barcode regions of the polynucleotides configured are such that the primer is extended to the end of the barcode region across the plurality of polynucleotides before being extended into the homopolymer region. According to some methods, two primers or a cleavable primer is used to separately sequence the barcode region and the target region.
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公开(公告)号:US20230022124A1
公开(公告)日:2023-01-26
申请号:US17713934
申请日:2022-04-05
Applicant: Ultima Genomics, Inc.
Inventor: Gilad ALMOGY , Linda LEE
IPC: C12Q1/6869 , C12Q1/6806
Abstract: The present disclosure provides methods and systems for nucleic acid sequencing. Such systems and methods may achieve context-independent incorporation, have reduced context-dependence or have context-dependence that is amenable to calibration and modeling. Such systems and methods may also reduce misincorporation.
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公开(公告)号:US11512350B2
公开(公告)日:2022-11-29
申请号:US17089781
申请日:2020-11-05
Applicant: Ultima Genomics, Inc.
Inventor: Gilad Almogy , Kristopher Barbee , Nathan Beckett
IPC: C12Q1/6874 , C12Q1/6809 , C12Q1/6825 , B01J19/00 , B01L3/00 , G01N33/543 , C12Q1/6834
Abstract: Provided are methods for biological sample processing and analysis. A method can comprise providing a substrate configured to rotate. The substrate can comprise an array having immobilized thereto a biological analyte. A solution comprising a plurality of probes may be directed, via centrifugal force, across the substrate during rotation of the substrate, to couple at least one of the plurality of probes with the biological analyte. A detector can be configured to detect a signal from the at least one probe coupled to the biological analyte, thereby analyzing the biological analyte.
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公开(公告)号:US11377680B2
公开(公告)日:2022-07-05
申请号:US17395382
申请日:2021-08-05
Applicant: Ultima Genomics, Inc.
Inventor: Linda G. Lee , Gilad Almogy , Steven Menchen
IPC: C12Q1/68 , C12Q1/6823 , C12Q1/6869 , C12Q1/6876
Abstract: The present disclosure provides labeling reagents for labeling substrates such as nucleotides, proteins, antibodies, lipids, and cells. The labeling reagents provided herein may comprise fluorescent labels and semi-rigid linkers. Methods for nucleic acid sequencing using materials comprising such labeling reagents are also provided here.
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公开(公告)号:US11276480B2
公开(公告)日:2022-03-15
申请号:US17406464
申请日:2021-08-19
Applicant: ULTIMA GENOMICS, INC.
Inventor: Mark Pratt , Gilad Almogy , Avishai Bartov
IPC: G16B40/10 , G16B30/10 , G16B45/00 , C12Q1/6806 , C12Q1/6869
Abstract: The present disclosure provides methods and systems for accurate and efficient context-aware base calling of sequences. In an aspect, disclosed herein is a method for sequencing a nucleic acid molecule, comprising: (a) sequencing the nucleic acid molecule to generate a plurality of sequence signals; and (b) determining base calls of the nucleic acid molecule based at least in part on (i) the plurality of sequence signals and (ii) quantified context dependency for at least a portion of the plurality of sequence signals.
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公开(公告)号:US20210147931A1
公开(公告)日:2021-05-20
申请号:US17158960
申请日:2021-01-26
Applicant: Ultima Genomics, Inc.
Inventor: Florian OBERSTRASS , Gilad ALMOGY
IPC: C12Q1/6874 , C12N15/10
Abstract: Described herein are methods for determining a sequence of a region of interest from an mRNA molecule. Sequenced polynucleotides can include a barcode region, a homopolymer region (e.g., a poly-A region), and a target region associated with the mRNA molecule. According to some methods, the barcode region omits the same base present in the homopolymer region. According to some methods, extension of the primer used for sequencing is stalled within the homopolymer region. According to some methods, sequencing flow cycles and the different barcode regions of the polynucleotides configured are such that the primer is extended to the end of the barcode region across the plurality of polynucleotides before being extended into the homopolymer region. According to some methods, two primers or a cleavable primer is used to separately sequence the barcode region and the target region.
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公开(公告)号:US20210079464A1
公开(公告)日:2021-03-18
申请号:US16953071
申请日:2020-11-19
Applicant: Ultima Genomics, Inc.
Inventor: Nathan BECKETT , Gilad ALMOGY , Nathan CASWELL , Jacob A. WOLF , Kristopher BARBEE , Denis PRINTINSKI , Mark PRATT , Gene POLOVY , Osip SCHWARTZ , Stephanie KUBECKA , Steven MENCHEN , Joseph ANTHONY , Jose Martin SOSA , Phillip You Fai LEE
IPC: C12Q1/6874 , G01N35/10
Abstract: Provided are systems and methods for analyte detection and analysis. A system can comprise an open substrate. The open substrate may be configured to rotate or otherwise move. The open substrate can comprise an array of individually addressable locations, with analytes immobilized thereto. The substrate may be spatially indexed to identify nucleic acid molecules from one or more sources, and/or sequences thereof, with the respective one or more sources. A solution comprising a plurality of probes may be directed across the array to couple at least one of the plurality of probes with at least one of the analytes to form a bound probe. A detector can be configured to detect a signal from the bound probe via scanning of the substrate while minimizing temperature fluctuations of the substrate or optical aberrations caused by bubbles.
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