Analysis system and analysis method

1. An analysis system comprising:

an analyzer configured to separate a sample including a plurality of components by chromatography, wherein the plurality of components comprise M kinds of components each of which is labeled with a different fluorescent substance, wherein the M is an integer greater than 1, and acquire first time-series data of fluorescence signals detected in N kinds of wavelength bands for each of the different fluorescent substances, wherein N is an integer greater than 1 and M is greater than the N, in a state in which at least a portion of the plurality of components is not completely separated;

a storage device configured to store second time-series data of individual model fluorescence signals of each of the M kinds of components each of which is labeled with the different fluorescent substance detected in the N kinds of wavelength bands, each second time-series data of the individual model fluorescence signals of each of the M kinds of components indicates a temporal change in fluorescence intensity in the N kinds of wavelength bands;

a processor coupled to the storage device; and

a memory coupled to the processor storing instructions, that when executed by the processor, configure the processor to:

store the acquired first time-series data having the detected fluorescence signals, the detected fluorescence signals including detected fluorescence signals of two or more of the M kinds of components in a space-time overlap,

perform fitting of peaks of the first time-series data with peaks of the second time-series data of each of the individual model fluorescence signals of each of the M kinds of components, and

determine which of the M kinds of components each of the plurality of components recognized in the first time-series data is based on the fitting of the first time-series data with the second time-series data of each of the individual model fluorescence signals of each of the M kinds of components.

2. The analysis system according to claim 1 ,

wherein the processor is configured to output third time-series data of a concentration of each of the plurality of components recognized in the first time-series data by fitting the second time-series data to the first time-series data.

3. The analysis system according to claim 2 ,

wherein the storage device stores mobility difference data relating to a difference in mobility between the M kinds of components each of which is labeled with the different fluorescent substance, and

wherein the processor is configured to correct differences in mobility in the third time-series data based on the mobility difference data.

4. The analysis system according to claim 2 ,

wherein the processor is configured to output fitting error data or fitting accuracy data relating to a difference between the first time-series data and a result of the fitting on each of the plurality of components.

5. The analysis system according to claim 4 , further comprising:

a display coupled to the processor,

wherein the processor is configured to display, on the display, at least one of:

(i) the result of the fitting relating to each of the plurality of components,

(ii) fitting error data or fitting accuracy data relating to each of the plurality of components, and

(iii) the third time-series data.

6. The analysis system according to claim 1 ,

wherein the plurality of components are nucleic acid fragments of different lengths or of different compositions, and

wherein the chromatography is electrophoresis.

7. The analysis system according to claim 6 ,

wherein the plurality of components are DNA fragments prepared by a Sanger method using a target DNA as a template, wherein the DNA fragments comprise four kinds of DNA fragments respectively terminally labeled with four kinds of fluorescent substances according to terminal base species,

wherein the first time-series data is time-series data of fluorescence signals detected in three kinds or two kinds of wavelength bands, and

wherein the processor is configured to determine a base sequence of the target DNA.

8. The analysis system of claim 1 ,

wherein the fitting of the peaks of the first time-series data with peaks of the second time-series data is performed by changing a height and a time of each second time-series data of the individual model fluorescence signals.

9. An analysis method comprising:

separating a sample including a plurality of components by chromatography wherein the plurality of components comprise M kinds of components each of which is labeled with a different fluorescent substance, wherein the M is an integer greater than 1;

acquiring first time-series data of fluorescence signals detected in N kinds of wavelength bands for each of the different fluorescent substances, wherein N is an integer greater than 1 and M is greater than the N, in a state in which at least a portion of the plurality of components is not completely separated;

storing second time-series data of individual model fluorescence signals of each of the M kinds of components each of which is labeled with the different of fluorescent substance detected in the N kinds of wavelength bands, each second time-series data of the individual model fluorescence signals of each of the M kinds of components indicates a temporal change in fluorescence intensity in the N kinds of wavelength bands;

storing the acquired first time-series data having the detected fluorescence signals, the detected fluorescence signals including detected fluorescence signals of two or more of the M kinds of components in a space-time overlap;

performing fitting of peaks of the first time-series data with peaks of the second time-series data of each of the individual model fluorescence signals of each of the M kinds of components; and

determining which of the M kinds of components each of the plurality of components recognized in the first-time series data is based on the fitting of the first time-series data with the second time-series data of each of the individual model fluorescence signals of each of the M kinds of components.

10. The analysis method according to claim 9 , further comprising:

outputting third time-series data of a concentration of each of the plurality of components recognized in the first time-series data by fitting the second time-series data to the first time-series data.

11. The analysis method according to claim 10 , further comprising:

storing mobility difference data relating to a difference in mobility between the M kinds of components each of which is labeled with the different fluorescent substance,

wherein the determining includes correcting differences in mobility in the third time-series data based on the mobility difference data.

12. The analysis method according to claim 10 ,

wherein the determining includes outputting fitting error data or fitting accuracy data relating to a difference between the first time-series data and a result of the fitting on each of the plurality of components.

13. The analysis method according to claim 12 , further comprising displaying at least one of:

(i) the result of the fitting relating to each of the plurality of components,

(ii) fitting error data or fitting accuracy data relating to each of the plurality of components, and

(iii) the third time-series data.

14. The analysis method according to claim 9 ,

wherein the plurality of components are nucleic acid fragments of different lengths or of different compositions, and

wherein the chromatography is electrophoresis.

15. The analysis method according to claim 14 ,

wherein the plurality of components are DNA fragments prepared by a Sanger method using a target DNA as a template, wherein the DNA fragments comprise four kinds of DNA fragments respectively terminally labeled with four kinds of fluorescent substances according to terminal base species,

wherein the first time-series data is time-series data of fluorescence signals detected in three kinds or two kinds of wavelength bands, and

wherein the determining includes determining a base sequence of the target DNA.

16. The analysis method of claim 9 ,

wherein the fitting of the peaks of the first time-series data with peaks of the second time-series data is performed by changing a height and a time of each second time-series data of the individual model fluorescence signals.