Intel Corporation

Illumina Corporation

Illumina Cambridge Limited

University of California

Boyan Boyanov

Anand S Murthy

Robert S Chau

Kevin L Gunderson

Brian S Doyle

Jingwei Bai

Jeffrey G Mandell

M Shane Bowen

Maria Candelaria Rogert Bacigalupo

Kanwal Jit Singh

Liangliang Qiang

Suman Datta

Glenn A Glass

Tarun Kumar Khurana

Been-Yih Jin

Hai Quang Tran

Grant M Kloster

Jeffrey S Fisher

Dale Buermann

Shaofeng Yu

Alex Aravanis

Darren Segale

Behnam Javanmardi

Brian Douglas Mather

Alexander Hsiao

James S Clarke

Alan M Myers

Andrew Antony Brown

Wayne N George

Hod Finkelstein

Cheng Frank Zhong

Dietrich A Dehlinger

Hyun-Mog Park

Lewis J Kraft

Sang Ryul Park

Ludovic Vincent

Thomas Hoffmann

Justin Fullerton

Sahngki Hong

Jack T Kavalieros

Justin K Brask

Jonathan Mark Boutell

Roberto Rigatti

Matthew William Kellinger

Cheng-Yao Chen

Poorya Sabounchi

Makarem A Hussein

John M Beierle

Klaus Maisinger

Ravindra Soman

Bradley Baas

Thomas Hoffman

Matthew V Metz

Mark L Doczy

Sebastian Bohm

Scott A Hareland

Michael D Goodner

Nick Lindert

Jens H Gundlach

Cyril Delattre

Majid Aghababazadeh

Tracy Helen Fung

Sergio Peisajovich

Kay Klausing

Xiuyu Cai

Andrew N Westmeyer

Kevan Samiee

Michel Perbost

Lea Pickering

Vijay Ramachandrarao

Lisa Kwok

Craig M Ciesla

Steven Mark Barnard

Dajun Yuan

Steven J Keating

Jeffery D Bielefeld

Vijayakumar S Ramachandrarao

Mansour Moinpour

Sridhar Balakrishnan

Philip G Collins

Gregory A Weiss

Rohan N Akolkar

Rico Otto

Kaitlin Pugliese

Vijayakumar SubramanyaRao RamachandraRao

Anthony Flannery

Gerald Kreindl

Rean Silke Musa

Sang Park

Hai Tran

Jens Gundlach

Cyril De Lattre

Anand Murphy

Devices for sequencing biopolymers and methods of using the devices are disclosed. In one example, such a device has a nanopore, a plurality of wells and fluidic tunnels to allow a biopolymer to translocate in the device. In some embodiments, the device may include integrated electronics or micro-electromechanical systems, such as valves, bubble generators/annihilators or pressure pulse generators, to actively control fluidic/ionic/electric flows in the device.

Isolation of cells in a nanopore sensor array

The present disclosure relates to the field of molecular biology and more specifically to microarrays and methods. In particular, the present disclosure relates to a method for amplifying a nucleic acid on a substrate comprising at least one well, the method includes: depositing a plurality of first capture primer pairs and a plurality of second capture primer pairs in a layer at least partially covering the inner well surface, wherein the primer density of first capture primer pairs is higher than the primer density of second primer pairs; contacting a sample comprising a plurality of target polynucleotides with the substrate under conditions sufficient for a single target polynucleotide per well to hybridize with a capture primer of the second capture primer pair; and performing a kinetic exclusion assay (KEA) to produce a monoclonal population of amplicons from the single target polynucleotide.

Methods and arrays for producing and sequencing monoclonal clusters of nucleic acid

An example sensor includes a flow cell, a detection device, and a controller. The flow cell includes a passivation layer having opposed surfaces and a reaction site at a first of the opposed surfaces. The flow cell also includes a lid operatively connected to the passivation layer to partially define a flow channel between the lid and the reaction site. The detection device is in contact with a second of the opposed surfaces of the passivation layer, and includes an embedded metal layer that is electrically isolated from other detection circuitry of the detection device. The controller is to ground the embedded metal layer.

Sensors having integrated protection circuitry

Systems and methods for conducting designated reactions utilizing a base instrument and a removable cartridge. The removable cartridge includes a fluidic network that receives and fluidically directs a biological sample to conduct the designated reactions. The removable cartridge also includes a flow-control valve that is operably coupled to the fluidic network and is movable relative to the fluidic network to control flow of the biological sample therethrough. The removable cartridge is configured to separably engage a base instrument. The base instrument includes a valve actuator that engages the flow-control valve of the removable cartridge. A detection assembly held by at least one of the removable cartridge or the base instrument may be used to detect the designated reactions.

Systems and methods for biochemical analysis including a base instrument and a removable cartridge

Biosensor including a device base having a sensor array of light sensors and a guide array of light guides. The light guides have input regions that are configured to receive excitation light and light emissions generated by biological or chemical substances. The light guides extend into the device base toward corresponding light sensors and have a filter material. The device base includes device circuitry electrically coupled to the light sensors and configured to transmit data signals. A passivation layer extends over the device base and forms an array of reaction recesses above the light guides. The biosensor also includes peripheral crosstalk shields that at least partially surround corresponding light guides of the guide array to reduce optical crosstalk between adjacent light sensors.

Biosensors for biological or chemical analysis and methods of manufacturing the same

In an example, a sensing system includes a pH sensor. The pH sensor includes two electrodes and a conductive channel operatively connected to the two electrodes. A complex is attached to the conductive channel of the pH sensor. The complex includes a polymerase linked to at least one pH altering moiety that is to participate in generating a pH change within proximity of the conductive channel from consumption of a secondary substrate in a fluid that is exposed to the pH sensor. The at least one pH altering moiety is selected from the group consisting of an enzyme, a metal coordination complex, a co-factor, and an activator.

Sensing systems

An example of a flow cell includes a substrate; a first primer set attached to a first region on the substrate, the first primer set including an un-cleavable first primer and a cleavable second primer; and a second primer set attached to a second region on the substrate, the second primer set including a cleavable first primer and an un-cleavable second primer.

Flow cells

Devices and methods of using the devices are disclosed which can provide scalability, improved sensitivity and reduced noise for sequencing polynucleotide. Examples of the devices include a biological or solid-state nanopore, a field effect transistor (FET) sensor with improved gate controllability over the channel, and a porous structure.

Devices with field effect transistors

Systems and methods for conducting designated reactions that include a fluidic network having a sample channel, a reaction chamber, and a reservoir. The sample channel is in flow communication with a sample port. The system also includes a rotary valve that has a flow channel and is configured to rotate between first and second valve positions. The flow channel fluidically couples the reaction chamber and the sample channel when the rotary valve is in the first valve position and fluidically couples the reservoir and the reaction chamber when the rotary valve is in the second valve position. A pump assembly induces a flow of a biological sample toward the reaction chamber when the rotary valve is in the first valve position and induces a flow of a reaction component from the reservoir toward the reaction chamber when the rotary valve is in the second valve position.

Systems and methods including a rotary valve for at least one of sample preparation or sample analysis

A sensing system includes a charge sensor including two electrodes and an electrically conductive channel connecting the two electrodes. The sensing system also includes a charged molecule attached to the electrically conductive channel. The charged molecule includes a recognition site to reversibly bind a label of a labeled nucleotide; has an unbound favored conformation associated with an unbound charge configuration; and has a favored conformation associated with a charge configuration when the recognition site is bound to the label. The charge configuration is different from the unbound charge configuration. The sensing system further includes a polymerase attached to the electrically conductive channel or to the charged molecule.

Example devices include a cis well associated with a cis electrode, a trans well associated with a trans electrode, and a field effect transistor (FET) positioned between the cis well and the trans well. Examples of the field effect transistor (FET) include a fluidic system defined therein. The fluidic system includes a first cavity facing the cis well, a second cavity fluidically connected to the trans well, and a through via extending through the field effect transistor from the first cavity. A first nanoscale opening fluidically connects the cis well and the first cavity, the first nanoscale opening having an inner diameter. A second nanoscale opening fluidically connects the through via and the second cavity, the second nanoscale opening having an inner diameter. The second nanoscale opening inner diameter is larger than the first nanoscale opening inner diameter.

Device for sequencing

The disclosure provides detection apparatus having one or more nanopores, methods for making apparatus having one or more nanopore and methods for using apparatus having one or more nanopores. Uses include, but are not limited to detection and sequencing of nucleic acids.

Hybrid nanopore sensors

The present disclosure relates to the field of molecular biology and more specifically to microarrays and methods, including methods for modifying immobilized capture primers comprising: a) contacting a substrate comprising a plurality of immobilized capture primers with a plurality of template nucleic acids under conditions sufficient for hybridization to produce one or more immobilized template nucleic acids, and b) extending one or more immobilized capture primers to produce one or more immobilized extension products complementary to the one or more template nucleic acid.

Growing community of inventors

Portland, OR, United States of America

Boyan Boyanov