公开(公告)号：US20150235334A1

公开(公告)日：2015-08-20

申请号：US14518757

申请日：2014-10-20

Applicant: Palantir Technologies Inc.

Inventor： Lekan Wang ,  Melody Hildebrandt ,  Tayler Cox ,  Chris Burchhardt ,  Casey Ketterling ,  Ajay Sudan ,  Bob McGrew ,  Jacob Albertson ,  Harkirat Singh ,  Shyam Sankar ,  Rick Ducott ,  Peter Maag ,  Marissa Kimball

IPC: G06Q50/22 ,  G06Q30/00

CPC classification number: G06Q50/22 ,  G06F21/50 ,  G06Q10/10 ,  G06Q30/018 ,  G06Q40/08

Abstract: Systems and techniques for sharing healthcare fraud data are described herein. Healthcare fraud detection schemes and/or fraud data may be automatically shared, investigated, enabled, and/or used by entities. A healthcare fraud detection scheme may be enabled on different entities comprising different computing systems to combat similar healthcare fraud threats, instances, and/or attacks. Healthcare fraud detection schemes and/or fraud data may be modified to redact sensitive information and/or configured through access controls for sharing.

Abstract translation: 本文描述了用于共享医疗欺诈数据的系统和技术。 医疗欺诈检测方案和/或欺诈数据可以被实体自动共享，调查，启用和/或使用。 可以在包括不同计算系统的不同实体上实现医疗欺诈检测方案，以对抗类似的医疗欺诈威胁，实例和/或攻击。 可以修改医疗保健欺诈检测方案和/或欺诈数据以修正敏感信息和/或通过用于共享的访问控制来配置。

公开(公告)号：US20140282177A1

公开(公告)日：2014-09-18

申请号：US13831791

申请日：2013-03-15

Applicant: PALANTIR TECHNOLOGIES, INC.

Inventor： Lekan Wang ,  Hyunghoon Cho ,  Abimanyu Raja ,  Elizabeth Caudill

IPC: G06F3/0481

CPC classification number: G06F19/26 ,  G06F3/0481 ,  G06F3/0482 ,  G06F3/04847 ,  G06F17/30864 ,  G06F19/28 ,  G06Q10/10

Abstract: Methods and computer apparatuses are disclosed for processing genomic data in at least partially automated workflows of modules. A method comprises: specifying a source from which nucleic acid sequence(s) are to be obtained; selecting module(s) for processing data, including at least one module for processing the one or more nucleic acid sequences; presenting, in a graphical user interface, graphical components representing the source and the module(s) as nodes within a workspace; receiving, via the graphical user interface, inputs arranging the source and the module(s) as a workflow comprising a series of nodes, the series indicating, for each particular module, that output from one of the source or another particular module is to be input into the particular module; generating an output for the workflow based upon the nucleic acid sequence(s) by processing each module in an order indicated by the series.

Abstract translation: 公开了用于在模块的至少部分自动化工作流程中处理基因组数据的方法和计算机装置。 一种方法包括：指定要获得核酸序列的来源; 选择用于处理数据的模块，包括用于处理所述一个或多个核酸序列的至少一个模块; 在图形用户界面中呈现作为工作空间内的节点的源和模块的图形组件; 通过图形用户界面接收将源和模块布置为包括一系列节点的工作流的输入，该系列针对每个特定模块指示来自源或另一个特定模块之一的输出将是 输入到特定模块; 通过按照该系列所示的顺序处理每个模块，基于核酸序列生成工作流的输出。

公开(公告)号：US20140278479A1

公开(公告)日：2014-09-18

申请号：US13949043

申请日：2013-07-23

Applicant: Palantir Technologies, Inc.

Inventor： Lekan Wang ,  Casey Ketterling ,  Michael Winlo ,  Christopher Ryan Luck

IPC: G06F19/00

CPC classification number: G06F19/328 ,  G06Q10/063 ,  G06Q50/22

Abstract: A system for, among other purposes, detecting health care fraud, comprises a data import component for importing health care data from data source(s) such health care providers, insurers, or pharmacies; data repositor(ies) in which the data import component creates health care objects such as provider objects that describe health care providers, patient objects that represent health care recipients, and health care event objects that describe one or more of: health care claims, prescriptions, medical procedures, or diagnoses; a correlation component that identifies correlations between the health care objects; a graph generator component that generates graphs of networks identified based at least on the correlations identified by the correlation component, the graphs comprising linked nodes that represent health care objects in the identified networks; and an interface generator that generates interfaces that display the graphs generated by the graph generator.

Abstract translation: 包括用于从医疗保健提供者，保险公司或药店等数据来源导入保健数据的数据导入部件，用于检测医疗保健欺诈的系统， 数据存储器（数据），其中数据导入组件创建医疗保健对象，例如描述医疗保健提供者的提供者对象，代表医疗保健者的患者对象以及描述以下一个或多个的医疗保健事件对象：医疗保健声明，处方 ，医疗程序或诊断; 识别卫生保健对象之间的相关性的相关分量; 图形生成器组件，其生成至少基于由相关组件识别的相关性所标识的网络的图，所述图包括表示所识别的网络中的医疗保健对象的链接节点; 以及一个接口生成器，用于生成显示图形生成器生成的图形的接口。

公开(公告)号：US11676686B2

公开(公告)日：2023-06-13

申请号：US17355711

申请日：2021-06-23

Applicant: Palantir Technologies Inc.

Inventor： Lekan Wang ,  Hyunghoon Cho ,  Abimanyu Raja ,  Elizabeth Caudill

IPC: G16B45/00 ,  G06F16/951 ,  G16B50/00 ,  G06Q10/10 ,  G16B50/10 ,  G06F3/0481 ,  G06F3/0482 ,  G06F3/0484 ,  G06F3/04847

CPC classification number: G16B45/00 ,  G06F3/0481 ,  G06F3/0482 ,  G06F3/04847 ,  G06F16/951 ,  G06Q10/10 ,  G16B50/00 ,  G16B50/10

Abstract: Methods and computer apparatuses are disclosed for processing genomic data in at least partially automated workflows of modules. A method comprises: specifying a source from which nucleic acid sequence(s) are to be obtained; selecting module(s) for processing data, including at least one module for processing the one or more nucleic acid sequences; presenting, in a graphical user interface, graphical components representing the source and the module(s) as nodes within a workspace; receiving, via the graphical user interface, inputs arranging the source and the module(s) as a workflow comprising a series of nodes, the series indicating, for each particular module, that output from one of the source or another particular module is to be input into the particular module; generating an output for the workflow based upon the nucleic acid sequence(s) by processing each module in an order indicated by the series.

公开(公告)号：US20220277816A1

公开(公告)日：2022-09-01

申请号：US17681570

申请日：2022-02-25

Applicant: Palantir Technologies Inc.

Inventor： Michael Winlo ,  Chris Burchhardt ,  Kyle McLain ,  Harsh Pandey ,  Tayler Cox ,  Lekan Wang

IPC: G16H10/60 ,  G16H40/20

Abstract: Various systems and methods are provided that aggregate, analyze, and display health data for users. The system aggregates data stored in various databases. For example, the system retrieves data from these databases, maps the data to a set of common terms based on an ontology, and displays such information to an entity accessing the system. Rather than converting the data stored in the databases into a standardized format, the system includes a set of ontologies that provide a correlation between a first set of fields and a second set of fields. The system determines a correlation between a first field in the first set of fields and a second field in the second set of fields using the ontology, stores data retrieved from the database in a second database in association with the second field, and displays the data associated with the first field under the second field.

公开(公告)号：US20220222270A1

公开(公告)日：2022-07-14

申请号：US17710605

申请日：2022-03-31

Applicant: Palantir Technologies Inc.

Inventor： Matthew Owens ,  Andrew Girvin ,  Alice Venancio Marques Serra ,  Daniel Williams ,  Myles Gurule ,  Harishchandra Ramadas ,  James Evans ,  Lekan Wang ,  Megha Arora ,  Nelson D'Antonio ,  Shannon Barnes ,  Anthony Sherbakov

IPC: G06F16/26 ,  G06F16/28 ,  G06F16/248

Abstract: A system architecture for linking one or more derived objects to existing data objects in a data structure can be organized in a variety of forms. A method for establishing the architecture may include linking first and second data objects. linking first and second data objects. The first and second data objects may be associated with corresponding first and second pluralities of properties. The method may include receiving a first user limitation associated with at least one of the first or second pluralities of properties and receiving a second user limitation associated with at least one of the first or second pluralities of properties. The method can include deriving a conclusion object comprising a third plurality of properties comprising a subset of one or more of the first or second pluralities of properties and linking the conclusion object to the first and second data objects.

公开(公告)号：US11294928B1

公开(公告)日：2022-04-05

申请号：US16260633

申请日：2019-01-29

Applicant: Palantir Technologies Inc.

Inventor： Matthew Owens ,  Andrew Girvin ,  Alice Venancio Marques Serra ,  Daniel Williams ,  Myles Gurule ,  Harishchandra Ramadas ,  James Evans ,  Lekan Wang ,  Megha Arora ,  Nelson D'Antonio ,  Shannon Barnes ,  Anthony Sherbakov

IPC: G06F16/26 ,  G06F16/28 ,  G06F16/248

Abstract: A system architecture for linking one or more derived objects to existing data objects in a data structure can be organized in a variety of forms. A method for establishing the architecture may include linking first and second data objects. The first data object may include a first plurality of properties, and the second data object may include a second plurality of properties. At least one of the second plurality of properties may be based on the first plurality of properties. The method may further include receiving, by a computer, a user limitation of a property type that is associated with the at least one of the second plurality of properties. The method may include deriving, based on the user limitation, a new object that includes a third plurality of properties. The third plurality of properties may include a subset of one or more of the first and second pluralities of properties. The new object may be linked to the first and second data objects.

公开(公告)号：US09501202B2

公开(公告)日：2016-11-22

申请号：US13831791

申请日：2013-03-15

Applicant: Palantir Technologies, Inc.

Inventor： Lekan Wang ,  Hyunghoon Cho ,  Abimanyu Raja ,  Elizabeth Caudill

IPC: G06F3/0481 ,  G06F19/26 ,  G06F19/28 ,  G06Q10/10

CPC classification number: G06F19/26 ,  G06F3/0481 ,  G06F3/0482 ,  G06F3/04847 ,  G06F17/30864 ,  G06F19/28 ,  G06Q10/10

Abstract: Methods and computer apparatuses are disclosed for processing genomic data in at least partially automated workflows of modules. A method comprises: specifying a source from which nucleic acid sequence(s) are to be obtained; selecting module(s) for processing data, including at least one module for processing the one or more nucleic acid sequences; presenting, in a graphical user interface, graphical components representing the source and the module(s) as nodes within a workspace; receiving, via the graphical user interface, inputs arranging the source and the module(s) as a workflow comprising a series of nodes, the series indicating, for each particular module, that output from one of the source or another particular module is to be input into the particular module; generating an output for the workflow based upon the nucleic acid sequence(s) by processing each module in an order indicated by the series.

Abstract translation: 公开了用于在模块的至少部分自动化工作流程中处理基因组数据的方法和计算机装置。 一种方法包括：指定要获得核酸序列的来源; 选择用于处理数据的模块，包括用于处理所述一个或多个核酸序列的至少一个模块; 在图形用户界面中呈现作为工作空间内的节点的源和模块的图形组件; 通过图形用户界面接收将源和模块布置为包括一系列节点的工作流的输入，该系列针对每个特定模块指示来自源或另一个特定模块之一的输出将是 输入到特定模块; 通过按照该系列所示的顺序处理每个模块，基于核酸序列生成工作流的输出。