Inventor

AmirAli TALASAZ

Inventor

US

Overview

2021–2026

Patent span

Chemistry

Primary field (CPC C)

Patents· 58 as inventor

Public. Assignee & technology derived from the patent record. Each patent links to its LexDana page.

C12Qprimary

C12QMeasuring or testing processes involving enzymes, nucleic acids or microorganisms33%

G16BBioinformatics, i.e. information and communication technology [ict] specially adapted for genetic or protein-related data processing in computational molecular biology30%

G16HHealthcare informatics, i.e. information and communication technology [ict] specially adapted for the handling or processing of medical or healthcare data9%

C12NMicroorganisms or enzymes9%

C12MApparatus for enzymology or microbiology6%

G01NInvestigating or analysing materials by determining their chemical or physical properties6%

Y02ATechnologies for adaptation to climate change6%

A61KPreparations for medical, dental or toiletry purposes1%

C07KPeptides1%

PatentTitleYear

12,597,524Cancer evolution detection and diagnostic2026 12,571,053Methods for early detection of cancer2026 12,571,055Methods for early detection of cancer2026 12,565,674Methods and systems for analyzing nucleic acid molecules2026 12,435,368Methods and systems for detecting genetic variants2025 12,428,670Methods and systems for analyzing nucleic acid molecules2025 12,359,245Methods and systems for analyzing nucleic acid molecules2025 12,319,972Methods for monitoring residual disease2025 D1077824Display screen or portion thereof with graphical user interface2025 12,319,968Gene mutations and copy number alterations of EGFR, KRAS and MET2025 12,319,961Methods and systems for detecting genetic variants2025 12,286,672Methods and systems for detecting genetic variants2025 12,281,354Systems and methods to detect rare mutations and copy number variation2025 12,258,626Methods and systems for detecting genetic variants2025 12,252,749Systems and methods to detect rare mutations and copy number variation2025 12,241,128Methods for early detection of cancer2025 12,116,624Systems and methods to detect rare mutations and copy number variation2024 12,116,640Methods for early detection of cancer2024 12,110,560Methods for monitoring residual disease2024 12,098,421Methods and systems for detecting genetic variants2024 12,098,422Methods and systems for detecting genetic variants2024 12,054,783Systems and methods to detect rare mutations and copy number variation2024 12,054,774Methods and systems for detecting genetic variants2024 12,049,673Systems and methods to detect rare mutations and copy number variation2024 12,024,745Methods and systems for detecting genetic variants2024 12,024,746Methods and systems for detecting genetic variants2024 11,996,202Cancer evolution detection and diagnostic2024 11,959,139Methods and systems for detecting genetic variants2024 11,952,616Methods and systems for analyzing nucleic acid molecules2024 11,913,065Systems and methods to detect rare mutations and copy number variation2024 11,879,158Systems and methods to detect rare mutations and copy number variation2024 11,827,942Methods for early detection of cancer2023 11,788,153Methods for early detection of cancer2023 11,773,453Systems and methods to detect rare mutations and copy number variation2023 11,767,556Methods and systems for detecting genetic variants2023 11,767,555Methods and systems for detecting genetic variants2023 11,756,655Population based treatment recommender using cell free DNA2023 11,667,959Systems and methods to detect rare mutations and copy number variation2023 11,667,967Methods and systems for detecting genetic variants2023 11,649,491Methods and systems for detecting genetic variants2023 11,643,694Methods for early detection of cancer2023 11,639,526Methods and systems for detecting genetic variants2023 11,639,525Methods and systems for detecting genetic variants2023 11,621,083Cancer evolution detection and diagnostic2023 11,519,039Methods for computer processing sequence reads to detect molecular residual disease2022 11,519,019Methods and systems for analyzing nucleic acid molecules2022 11,447,813Systems and methods to detect rare mutations and copy number variation2022 11,434,523Systems and methods to detect rare mutations and copy number variation2022 11,434,531Methods and systems for detecting genetic variants2022 11,359,248Methods for detecting single nucleotide variants or indels by deep sequencing2022 11,345,968Methods for computer processing sequence reads to detect molecular residual disease2022 11,335,463Cancer evolution detection and diagnostic2022 11,319,597Systems and methods to detect rare mutations and copy number variation2022 11,319,598Systems and methods to detect rare mutations and copy number variation2022 11,282,610Cancer evolution detection and diagnostic2022 11,242,569Methods to determine tumor gene copy number by analysis of cell-free DNA2022 11,149,306Methods and systems for detecting genetic variants2021 11,149,307Methods and systems for detecting genetic variants2021

Career & activity timeline

Assembled from patent assignee/location history and declaration credentials.

2021–2026Patents assigned to GUARDANT HEALTH INC (58)· patent assignee history

2021–2026Based in US· patent location history

2024–2025Patents assigned to GUARDENT HEALTH INC (2)· patent assignee history

2025Patents assigned to UNIV TEXAS (1)· patent assignee history

Inventor activity

Assignee and location history derived from the patent record.

Assignees

Assignee	Patents	Span
GUARDANT HEALTH INC	58	2021–2026
GUARDENT HEALTH INC	2	2024–2025
UNIV TEXAS	1	2025

Locations

Location	Patents	Span
US	58	2021–2026