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公开(公告)号：EP3637422A1
公开(公告)日：2020-04-15
申请号：EP19199379.9
申请日：2014-03-14
发明人： YOUNG, Brian A. , MINARD-SMITH, Angela T. , HEIZER, Esley M. Jr. , BORNMAN, Daniel M. , HESTER, Mark E. , YANG, Boyu
摘要： In one illustrative embodiment, a method may comprise receiving a first text-based computer file including one or more records, each of the one or more records comprising nucleotide sequence data generated by a read of a massively parallel sequencing instrument, determining whether a portion of the nucleotide sequence data of each record represents a short tandem repeat (STR) associated with a locus, placing each portion of the nucleotide sequence data determined to represent an STR associated with a locus into one of a number of locus-specific lists, determining a number of occurrences within each locus-specific list of identical nucleotide sequence data representing a unique STR, and generating a second text-based computer file including one or more records, each of the one or more records corresponding to a unique STR for which the number of occurrences of identical nucleotide sequence data representing the unique STR exceeded an abundance threshold.
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公开(公告)号：EP4386763A2
公开(公告)日：2024-06-19
申请号：EP23217163.7
申请日：2014-03-14
发明人： YOUNG, Brian A. , MINARD-SMITH, Angela T. , HEIZER, Esley M., Jr. , BORNMAN, Daniel M. , HESTER, Mark E. , YANG, Boyu
IPC分类号： G16B30/00
摘要： In one illustrative embodiment, a method may comprise receiving a first text-based computer file including one or more records, each of the one or more records comprising nucleotide sequence data generated by a read of a massively parallel sequencing instrument, determining whether a portion of the nucleotide sequence data of each record represents a short tandem repeat (STR) associated with a locus, placing each portion of the nucleotide sequence data determined to represent an STR associated with a locus into one of a number of locus-specific lists, determining a number of occurrences within each locus-specific list of identical nucleotide sequence data representing a unique STR, and generating a second text-based computer file including one or more records, each of the one or more records corresponding to a unique STR for which the number of occurrences of identical nucleotide sequence data representing the unique STR exceeded an abundance threshold.
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3.发明公开COMPUTER FILES AND METHODS SUPPORTING FORENSIC ANALYSIS OF NUCLEOTIDE SEQUENCE DATA 审中-公开电脑文件与方法，可支持核苷酸塞克斯·达塔取证分析
公开(公告)号：EP2973134A1
公开(公告)日：2016-01-20
申请号：EP14716722.5
申请日：2014-03-14
发明人： YOUNG, Brian, A. , MINARD-SMITH, Angela, T. , HEIZER, Esley, M., Jr. , BORNMAN, Daniel, M. , HESTER, Mark, E. , YANG, Boyu
CPC分类号： G06F19/22
摘要： In one illustrative embodiment, a method may comprise receiving a first text-based computer file including one or more records, each of the one or more records comprising nucleotide sequence data generated by a read of a massively parallel sequencing instrument, determining whether a portion of the nucleotide sequence data of each record represents a short tandem repeat (STR) associated with a locus, placing each portion of the nucleotide sequence data determined to represent an STR associated with a locus into one of a number of locus- specific lists, determining a number of occurrences within each locus-specific list of identical nucleotide sequence data representing a unique STR, and generating a second text-based computer file including one or more records, each of the one or more records corresponding to a unique STR for which the number of occurrences of identical nucleotide sequence data representing the unique STR exceeded an abundance threshold.
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公开(公告)号：EP4386763A3
公开(公告)日：2024-08-14
申请号：EP23217163.7
申请日：2014-03-14
发明人： YOUNG, Brian A. , MINARD-SMITH, Angela T. , HEIZER, Esley M., Jr. , BORNMAN, Daniel M. , HESTER, Mark E. , YANG, Boyu
摘要： In one illustrative embodiment, a method may comprise receiving a first text-based computer file including one or more records, each of the one or more records comprising nucleotide sequence data generated by a read of a massively parallel sequencing instrument, determining whether a portion of the nucleotide sequence data of each record represents a short tandem repeat (STR) associated with a locus, placing each portion of the nucleotide sequence data determined to represent an STR associated with a locus into one of a number of locus-specific lists, determining a number of occurrences within each locus-specific list of identical nucleotide sequence data representing a unique STR, and generating a second text-based computer file including one or more records, each of the one or more records corresponding to a unique STR for which the number of occurrences of identical nucleotide sequence data representing the unique STR exceeded an abundance threshold.
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