专利检索 ap:"FIVE3 GENOMICS LLC" 第 3 页

21.

发明公开
SYSTEMS AND METHODS FOR TRANSMISSION AND PRE-PROCESSING OF SEQUENCING DATA 审中-公开
标题翻译：系统和方法用于传送和测序数据进行预处理

公开(公告)号：EP3069285A1

公开(公告)日：2016-09-21

申请号：EP14862192.3

申请日：2014-11-13

申请人： Five3 Genomics, LLC

发明人： BENZ, Stephen Charles , SANBORN, John Zachary , VASKE, Charles Joseph

IPC分类号： G06F19/10

CPC分类号： H04L67/06 , G06F17/30076 , G06F19/22 , G06F19/28

摘要： "Omic" digital data transport systems and methods are disclosed. The disclosed systems and methods employ a transport server that assembles a transport group larger numbers of omic output files on the basis of machine specific annotation from one or more sequencing devices and user input related to one or more attributes for the omic output files.

22.

发明公开
DISTRIBUTED SYSTEM PROVIDING DYNAMIC INDEXING AND VISUALIZATION OF GENOMIC DATA 审中-公开
标题翻译：分布式面向动态索引和基因组数据的可视化

公开(公告)号：EP2788861A1

公开(公告)日：2014-10-15

申请号：EP12856007.5

申请日：2012-12-07

申请人： Five3 Genomics, LLC

发明人： VASKE, Charles Joseph , SANBORN, John Zachary , BENZ, Stephen

IPC分类号： G06F7/06

CPC分类号： G06T3/40 , G06F19/22 , G06F19/26 , G06F19/28 , G06T2200/24 , G09G5/373 , G09G2340/045 , G09G2354/00

摘要： Systems and methods for dynamic visualization of genomic data are provided in which a genomic visualization system adapts presentation of information content according to scale-relevant annotations within a sequence object.

23.

发明公开
MDM2-CONTAINING DOUBLE MINUTE CHROMOSOMES AND METHODS THEREFORE 审中-公开
标题翻译： MDM2-HALTIGE DOPPELMINUTENCHROMOSOMEN UND VERFAHRENDAFÜR

公开(公告)号：EP2788770A1

公开(公告)日：2014-10-15

申请号：EP12854939.1

申请日：2012-12-07

申请人： Five3 Genomics, LLC

发明人： SANBORN, John Zachary , VASKE, Charles Joseph , BENZ, Stephen Charles

IPC分类号： G01N33/574

CPC分类号： C12Q1/6886 , C12Q1/6869 , C12Q2600/106 , C12Q2600/172 , G06F19/00 , G06F19/18 , G06F19/22 , G06F19/24 , G16H50/20

摘要： Contemplated systems and methods allow for computational genomic analysis using paired-end sequence analysis and split read refinement to thereby identify high-confidence breakpoints associated with high copy numbers and orientation of rearrangements, which is then the basis for full reconstruction of double minutes (DM). In especially preferred aspects, the DM will also include an oncogene or tumor suppressor gene, and/or may be found in blood or blood derived fluids.

摘要翻译： 考虑的系统和方法允许使用配对末端序列分析和分裂读取细化进行计算基因组分析，从而识别与高拷贝数和重排的取向相关联的高可信度断点，这是完全重建双分钟（DM）的基础，。在特别优选的方面，DM还将包括致癌基因或肿瘤抑制基因，和/或可以在血液或血液衍生的流体中发现。