Method for determining the presence or absence of minimal residual disease (MRD) in a subject who has been treated for a disease
The present invention is focused on a method, kit and system for determining the presence or absence of minimal residual disease in a subject who has been treated for a proliferative disease wherein said method, kit and system comprise:(A) amplifying and sequencing at least one nucleotide sequence c...
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creator | Rapado Martinez, María Inmaculada Barrio García, Santiago Onecha De La Fuente, Maria Esther Paz-Ares Rodriguez, Luis Martínez López, Joaquín Ayala Díaz, Rosa María Garrido Martín, Eva María |
description | The present invention is focused on a method, kit and system for determining the presence or absence of minimal residual disease in a subject who has been treated for a proliferative disease wherein said method, kit and system comprise:(A) amplifying and sequencing at least one nucleotide sequence comprised in genomic DNA from a biological sample obtained from said subject prior to treatment for said disease, to obtain a first list of characters reading from left to right;(B) amplifying and sequencing at least one nucleotide sequence comprised in genomic DNA from a biological sample obtained from said subject after treatment for said disease, to obtain a second list of characters reading from left to right,wherein when a nucleotide sequence is mutated it is a genetic marker for said proliferative disease;(C) determining, for each second list of characters obtained in step (B), the degree of similarity, DS, with each first list of characters obtained in step (A);(D) selecting, for each second list of characters obtained in step (B), the DS of highest value, DSHV;(E) adding up the number of second lists of characters which have a DSHV that is greater than a threshold value, T, to obtain Lc,(F) adding up the total number of second lists of characters, Lt;(G) calculating the level of minimal residual disease, MRD, according to any of the following formulae:MRD=(Lc×k)/(Lt×D)orMRD=Lc/LtorMRD=g×Lc×(D/k)/Lt2;(H) determining (i) the minimum variant read frequency, min VRF, of said genetic marker, (ii) the limit of detection, D-limit, of said genetic marker (iii) the average mutation noise, avMut and (iv) the average position noise, avPos;(I) determining the experimental sensitivity, ES, from the greater of the min VRF, D-limit, avMut and avPos or from the greater of min VRF and D-limit;(J) determining the presence or absence of minimal residual disease in said subject by comparing the value of the level of minimal residual disease with the value of ES, the values of min VRF, D-limit, avMut and avPos, or the values of min VRF and D-limit;wherein when said level of minimal residual disease is equal to or greater than said ES, min VRF, D-limit, avMut or avPos values, minimal residual disease is present in said subject. |
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Ayala Díaz, Rosa María ; Garrido Martín, Eva María</creator><creatorcontrib>Rapado Martinez, María Inmaculada ; Barrio García, Santiago ; Onecha De La Fuente, Maria Esther ; Paz-Ares Rodriguez, Luis ; Martínez López, Joaquín ; Ayala Díaz, Rosa María ; Garrido Martín, Eva María</creatorcontrib><description>The present invention is focused on a method, kit and system for determining the presence or absence of minimal residual disease in a subject who has been treated for a proliferative disease wherein said method, kit and system comprise:(A) amplifying and sequencing at least one nucleotide sequence comprised in genomic DNA from a biological sample obtained from said subject prior to treatment for said disease, to obtain a first list of characters reading from left to right;(B) amplifying and sequencing at least one nucleotide sequence comprised in genomic DNA from a biological sample obtained from said subject after treatment for said disease, to obtain a second list of characters reading from left to right,wherein when a nucleotide sequence is mutated it is a genetic marker for said proliferative disease;(C) determining, for each second list of characters obtained in step (B), the degree of similarity, DS, with each first list of characters obtained in step (A);(D) selecting, for each second list of characters obtained in step (B), the DS of highest value, DSHV;(E) adding up the number of second lists of characters which have a DSHV that is greater than a threshold value, T, to obtain Lc,(F) adding up the total number of second lists of characters, Lt;(G) calculating the level of minimal residual disease, MRD, according to any of the following formulae:MRD=(Lc×k)/(Lt×D)orMRD=Lc/LtorMRD=g×Lc×(D/k)/Lt2;(H) determining (i) the minimum variant read frequency, min VRF, of said genetic marker, (ii) the limit of detection, D-limit, of said genetic marker (iii) the average mutation noise, avMut and (iv) the average position noise, avPos;(I) determining the experimental sensitivity, ES, from the greater of the min VRF, D-limit, avMut and avPos or from the greater of min VRF and D-limit;(J) determining the presence or absence of minimal residual disease in said subject by comparing the value of the level of minimal residual disease with the value of ES, the values of min VRF, D-limit, avMut and avPos, or the values of min VRF and D-limit;wherein when said level of minimal residual disease is equal to or greater than said ES, min VRF, D-limit, avMut or avPos values, minimal residual disease is present in said subject.</description><language>eng</language><subject>BEER ; BIOCHEMISTRY ; CHEMISTRY ; COMPOSITIONS OR TEST PAPERS THEREFOR ; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL ORENZYMOLOGICAL PROCESSES ; ENZYMOLOGY ; INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTEDFOR SPECIFIC APPLICATION FIELDS ; MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEICACIDS OR MICROORGANISMS ; METALLURGY ; MICROBIOLOGY ; MUTATION OR GENETIC 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La Fuente, Maria Esther</creatorcontrib><creatorcontrib>Paz-Ares Rodriguez, Luis</creatorcontrib><creatorcontrib>Martínez López, Joaquín</creatorcontrib><creatorcontrib>Ayala Díaz, Rosa María</creatorcontrib><creatorcontrib>Garrido Martín, Eva María</creatorcontrib><title>Method for determining the presence or absence of minimal residual disease (MRD) in a subject who has been treated for a disease</title><description>The present invention is focused on a method, kit and system for determining the presence or absence of minimal residual disease in a subject who has been treated for a proliferative disease wherein said method, kit and system comprise:(A) amplifying and sequencing at least one nucleotide sequence comprised in genomic DNA from a biological sample obtained from said subject prior to treatment for said disease, to obtain a first list of characters reading from left to right;(B) amplifying and sequencing at least one nucleotide sequence comprised in genomic DNA from a biological sample obtained from said subject after treatment for said disease, to obtain a second list of characters reading from left to right,wherein when a nucleotide sequence is mutated it is a genetic marker for said proliferative disease;(C) determining, for each second list of characters obtained in step (B), the degree of similarity, DS, with each first list of characters obtained in step (A);(D) selecting, for each second list of characters obtained in step (B), the DS of highest value, DSHV;(E) adding up the number of second lists of characters which have a DSHV that is greater than a threshold value, T, to obtain Lc,(F) adding up the total number of second lists of characters, Lt;(G) calculating the level of minimal residual disease, MRD, according to any of the following formulae:MRD=(Lc×k)/(Lt×D)orMRD=Lc/LtorMRD=g×Lc×(D/k)/Lt2;(H) determining (i) the minimum variant read frequency, min VRF, of said genetic marker, (ii) the limit of detection, D-limit, of said genetic marker (iii) the average mutation noise, avMut and (iv) the average position noise, avPos;(I) determining the experimental sensitivity, ES, from the greater of the min VRF, D-limit, avMut and avPos or from the greater of min VRF and D-limit;(J) determining the presence or absence of minimal residual disease in said subject by comparing the value of the level of minimal residual disease with the value of ES, the values of min VRF, D-limit, avMut and avPos, or the values of min VRF and D-limit;wherein when said level of minimal residual disease is equal to or greater than said ES, min VRF, D-limit, avMut or avPos values, minimal residual disease is present in said subject.</description><subject>BEER</subject><subject>BIOCHEMISTRY</subject><subject>CHEMISTRY</subject><subject>COMPOSITIONS OR TEST PAPERS THEREFOR</subject><subject>CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL ORENZYMOLOGICAL PROCESSES</subject><subject>ENZYMOLOGY</subject><subject>INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTEDFOR SPECIFIC APPLICATION FIELDS</subject><subject>MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEICACIDS OR MICROORGANISMS</subject><subject>METALLURGY</subject><subject>MICROBIOLOGY</subject><subject>MUTATION OR GENETIC ENGINEERING</subject><subject>PHYSICS</subject><subject>PROCESSES OF PREPARING SUCH COMPOSITIONS</subject><subject>SPIRITS</subject><subject>VINEGAR</subject><subject>WINE</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2023</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqNjbsOwjAUQ7swIOAfLhsMDIGBsvISSxcec3WbuCSoTaokFSufThFlZ_KRfCwPk1eGqJ2i0nlSiPC1scbeKWpQ4xFgJajruOixpI9Rc0Vda1TbgTIBHECz7Lyfk7HEFNriARnpqR1pDlQAlqIHR3y_-LcaJ4OSq4BJn6Nkejxcd6cFGpcjNCxhEfPbRYh1KkS62S5X_zhvUsBHqw</recordid><startdate>20231010</startdate><enddate>20231010</enddate><creator>Rapado Martinez, María Inmaculada</creator><creator>Barrio García, Santiago</creator><creator>Onecha De La Fuente, Maria Esther</creator><creator>Paz-Ares Rodriguez, Luis</creator><creator>Martínez López, Joaquín</creator><creator>Ayala Díaz, Rosa María</creator><creator>Garrido Martín, Eva María</creator><scope>EVB</scope></search><sort><creationdate>20231010</creationdate><title>Method for determining the presence or absence of minimal residual disease (MRD) in a subject who has been treated for a disease</title><author>Rapado Martinez, María Inmaculada ; Barrio García, Santiago ; Onecha De La Fuente, Maria Esther ; Paz-Ares Rodriguez, Luis ; Martínez López, Joaquín ; Ayala Díaz, Rosa María ; Garrido Martín, Eva María</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_US11781189B23</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>2023</creationdate><topic>BEER</topic><topic>BIOCHEMISTRY</topic><topic>CHEMISTRY</topic><topic>COMPOSITIONS OR TEST PAPERS THEREFOR</topic><topic>CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL ORENZYMOLOGICAL PROCESSES</topic><topic>ENZYMOLOGY</topic><topic>INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTEDFOR SPECIFIC APPLICATION FIELDS</topic><topic>MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEICACIDS OR MICROORGANISMS</topic><topic>METALLURGY</topic><topic>MICROBIOLOGY</topic><topic>MUTATION OR GENETIC ENGINEERING</topic><topic>PHYSICS</topic><topic>PROCESSES OF PREPARING SUCH COMPOSITIONS</topic><topic>SPIRITS</topic><topic>VINEGAR</topic><topic>WINE</topic><toplevel>online_resources</toplevel><creatorcontrib>Rapado Martinez, María Inmaculada</creatorcontrib><creatorcontrib>Barrio García, Santiago</creatorcontrib><creatorcontrib>Onecha De La Fuente, Maria Esther</creatorcontrib><creatorcontrib>Paz-Ares Rodriguez, Luis</creatorcontrib><creatorcontrib>Martínez López, Joaquín</creatorcontrib><creatorcontrib>Ayala Díaz, Rosa María</creatorcontrib><creatorcontrib>Garrido Martín, Eva María</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Rapado Martinez, María Inmaculada</au><au>Barrio García, Santiago</au><au>Onecha De La Fuente, Maria Esther</au><au>Paz-Ares Rodriguez, Luis</au><au>Martínez López, Joaquín</au><au>Ayala Díaz, Rosa María</au><au>Garrido Martín, Eva María</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Method for determining the presence or absence of minimal residual disease (MRD) in a subject who has been treated for a disease</title><date>2023-10-10</date><risdate>2023</risdate><abstract>The present invention is focused on a method, kit and system for determining the presence or absence of minimal residual disease in a subject who has been treated for a proliferative disease wherein said method, kit and system comprise:(A) amplifying and sequencing at least one nucleotide sequence comprised in genomic DNA from a biological sample obtained from said subject prior to treatment for said disease, to obtain a first list of characters reading from left to right;(B) amplifying and sequencing at least one nucleotide sequence comprised in genomic DNA from a biological sample obtained from said subject after treatment for said disease, to obtain a second list of characters reading from left to right,wherein when a nucleotide sequence is mutated it is a genetic marker for said proliferative disease;(C) determining, for each second list of characters obtained in step (B), the degree of similarity, DS, with each first list of characters obtained in step (A);(D) selecting, for each second list of characters obtained in step (B), the DS of highest value, DSHV;(E) adding up the number of second lists of characters which have a DSHV that is greater than a threshold value, T, to obtain Lc,(F) adding up the total number of second lists of characters, Lt;(G) calculating the level of minimal residual disease, MRD, according to any of the following formulae:MRD=(Lc×k)/(Lt×D)orMRD=Lc/LtorMRD=g×Lc×(D/k)/Lt2;(H) determining (i) the minimum variant read frequency, min VRF, of said genetic marker, (ii) the limit of detection, D-limit, of said genetic marker (iii) the average mutation noise, avMut and (iv) the average position noise, avPos;(I) determining the experimental sensitivity, ES, from the greater of the min VRF, D-limit, avMut and avPos or from the greater of min VRF and D-limit;(J) determining the presence or absence of minimal residual disease in said subject by comparing the value of the level of minimal residual disease with the value of ES, the values of min VRF, D-limit, avMut and avPos, or the values of min VRF and D-limit;wherein when said level of minimal residual disease is equal to or greater than said ES, min VRF, D-limit, avMut or avPos values, minimal residual disease is present in said subject.</abstract><oa>free_for_read</oa></addata></record> 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subjects | BEER BIOCHEMISTRY CHEMISTRY COMPOSITIONS OR TEST PAPERS THEREFOR CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL ORENZYMOLOGICAL PROCESSES ENZYMOLOGY INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTEDFOR SPECIFIC APPLICATION FIELDS MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEICACIDS OR MICROORGANISMS METALLURGY MICROBIOLOGY MUTATION OR GENETIC ENGINEERING PHYSICS PROCESSES OF PREPARING SUCH COMPOSITIONS SPIRITS VINEGAR WINE |
title | Method for determining the presence or absence of minimal residual disease (MRD) in a subject who has been treated for a disease |
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