公开(公告)号：US20170132359A1

公开(公告)日：2017-05-11

申请号：US15295114

申请日：2016-10-17

Applicant: LIFE TECHNOLOGIES CORPORATION

Inventor： Alexander Joyner ,  Fiona Hyland ,  Heinz Breu

IPC: G06F19/22

CPC classification number: G16B30/00

Abstract: Systems and method for identifying somatic mutations can receive first and second sequence information, determine if a variant present in the first sequencing information is also present in the second sequence information, and identify variants present in the first sequence information are somatic mutations when the variant is either not present in the second sequence information or the presence of the variant in the second sequence information is likely due to a sequencing error.

公开(公告)号：US20230083827A1

公开(公告)日：2023-03-16

申请号：US17932712

申请日：2022-09-16

Applicant: LIFE TECHNOLOGIES CORPORATION

Inventor： Alexander Joyner ,  Fiona HYLAND ,  Heinz BREU

IPC: G16B20/20 ,  G16B30/00 ,  G16B30/10

Abstract: Systems and method for identifying somatic mutations can receive first and second sequence information, determine if a variant present in the first sequencing information is also present in the second sequence information, and identify variants present in the first sequence information are somatic mutations when the variant is either not present in the second sequence information or the presence of the variant in the second sequence information is likely due to a sequencing error.

公开(公告)号：US11468968B2

公开(公告)日：2022-10-11

申请号：US16434709

申请日：2019-06-07

Applicant: LIFE TECHNOLOGIES CORPORATION

Inventor： Alexander Joyner ,  Fiona Hyland ,  Heinz Breu

IPC: G16B20/20 ,  G16B30/00 ,  G16B30/10

Abstract: Systems and method for identifying somatic mutations can receive first and second sequence information, determine if a variant present in the first sequencing information is also present in the second sequence information, and identify variants present in the first sequence information are somatic mutations when the variant is either not present in the second sequence information or the presence of the variant in the second sequence information is likely due to a sequencing error.