Computing equipment, storage medium and thalassemia screening device and system

文档序号：1228041 发布日期：2020-09-08 浏览：6次中文

阅读说明：本技术 一种计算设备、存储介质和地中海贫血筛查装置及系统 (Computing equipment, storage medium and thalassemia screening device and system ) 是由王玉玺宋合兴李运涛周晓光于 2020-04-17 设计创作，主要内容包括：本发明公开一种计算设备、存储介质和地中海贫血筛查装置及系统。该计算设备,包括处理器和存储器,存储器中存储有程序,处理器执行程序时实现：接收受检者的待测样本的血红蛋白质谱图数据；对所述血红蛋白质谱图数据中的α珠蛋白链、β珠蛋白链和δ珠蛋白链的峰面积进行积分,分别计算δ珠蛋白链与β珠蛋白链峰面积之间的比值、δ珠蛋白链与α珠蛋白链峰面积之间的比值以及β珠蛋白链与α珠蛋白链峰面积之间的比值；根据所述δ珠蛋白链与β珠蛋白链峰面积之间的比值、δ珠蛋白链与α珠蛋白链峰面积之间的比值以及β珠蛋白链与α珠蛋白链峰面积之间的比值的相互关系,确定判定所述受检者是否患有地中海贫血症。(The invention discloses a computing device, a storage medium and a thalassemia screening device and system. The computing device comprises a processor and a memory, wherein the memory stores programs, and the processor executes the programs to realize that: receiving hemoglobin spectrogram data of a sample to be detected of a detected person; integrating peak areas of an alpha globin chain, a beta globin chain and a globin chain in the hemoglobin spectrogram data, and respectively calculating a ratio between peak areas of the globin chain and the beta globin chain, a ratio between peak areas of the globin chain and the alpha globin chain and a ratio between peak areas of the beta globin chain and the alpha globin chain; and determining whether the subject suffers from thalassemia or not according to the correlation of the ratio between the peak areas of the globin chain and the beta globin chain, the ratio between the peak areas of the globin chain and the alpha globin chain and the ratio between the peak areas of the beta globin chain and the alpha globin chain.)

1. A computing device comprising a processor and a memory, the memory having a program stored therein, the processor when executing the program implementing:

receiving hemoglobin spectrogram data of a sample to be detected of a detected person;

integrating peak areas of an alpha globin chain, a beta globin chain and a globin chain in the hemoglobin spectrogram data, and respectively calculating a ratio between peak areas of the globin chain and the beta globin chain, a ratio between peak areas of the globin chain and the alpha globin chain and a ratio between peak areas of the beta globin chain and the alpha globin chain;

and determining whether the subject suffers from thalassemia or not according to the correlation of the ratio between the peak areas of the globin chain and the beta globin chain, the ratio between the peak areas of the globin chain and the alpha globin chain and the ratio between the peak areas of the beta globin chain and the alpha globin chain.

2. The computing device of claim 1, wherein determining whether the subject has thalassemia comprises determining whether the subject has thalassemia from a correlation of the ratio between the globin chain and beta globin chain peak area, the ratio between globin chain and alpha globin chain peak area, and the ratio between beta globin chain and alpha globin chain peak area

If the peak area ratio of the globin chain to the beta globin chain is larger than a first threshold value, the peak area ratio of the globin chain to the alpha globin chain is larger than a second threshold value, and the peak area ratio of the beta globin chain to the alpha globin chain is smaller than a third threshold value, determining that the detected person is beta thalassemia; if the ratio of the globin chain peak area to the alpha globin chain peak area is less than the second threshold or the ratio of the beta globin chain peak area to the alpha globin chain peak area is greater than the third threshold, determining that the detected person is alpha thalassemia; if the peak area ratio of the globin chain to the beta globin chain is less than the first threshold, the peak area ratio of the globin chain to the alpha globin chain is greater than the second threshold, and the peak area ratio of the beta globin chain to the alpha globin chain is less than the third threshold, judging that the detected person is normal; otherwise, the examinee is judged to be suspected.

3. The computing device of claim 2,

the first threshold value is 11.0% + -0.5%, the second threshold value is 9.5% + -0.5%, and the third threshold value is 125.0% + -0.5%.

4. A storage medium storing a program, the program when executed implementing:

receiving hemoglobin spectrogram data of a sample to be detected of a detected person;

5. The storage medium of claim 4, wherein the determining whether the subject has thalassemia is determined according to a correlation of the ratio between the peak areas of the globin chain and the beta globin chain, the ratio between the peak areas of the globin chain and the alpha globin chain, and the ratio between the peak areas of the beta globin chain and the alpha globin chain comprises determining thalassemia

6. The storage medium of claim 5,

the first threshold value is 11.0% + -0.5%, the second threshold value is 9.5% + -0.5%, and the third threshold value is 125.0% + -0.5%.

7. A mediterranean anemia screening device is characterized by comprising

The matrix assisted laser desorption ionization time-of-flight mass spectrometer collects a sample to be detected of a detected person to obtain hemoglobin spectrogram data of the sample to be detected; and

the computing device of any of claims 1-3.

8. A mediterranean anemia screening system is characterized by comprising

The device of claim 7;

and the display is used for displaying the judgment result.

9. The system of claim 8, further comprising

And the micropipettor is used for dripping a sample to be detected of the detected person onto a target plate of the mass spectrometer.

Technical Field

The invention relates to the field of medical clinical detection. And more particularly to a computing device, storage medium, and thalassemia screening apparatus and system.

Background

Thalassemia, also known as thalassemia, is a hereditary hemolytic anemia, known as thalassemia. The causes of the disease are mainly due to deletion, mutation, etc. of alpha and beta genes. According to the gene cluster of the gene variation site, the disease can be divided into alpha globin aplastic anemia and beta globin aplastic anemia. The disease is widely distributed around the world, and southeast Asia is one of the high incidence areas. The incidence of diseases in Guangdong, Guangxi and Sichuan of China is high, and the incidence of diseases in the south provinces of the Yangtze river is gradually increased in recent years.

At present, clinical screening is mainly based on routine blood detection and hemoglobin electrophoresis analysis, and the clinical examination index is usually microcytic hypopigmented anemia and HbA accompanying the electrophoresis result₂Most of the thalassemia gene carriers have no obvious clinical pathological change due to different physiological changes caused by deletion or mutation of different types of genes, and particularly, the thalassemia gene carrier of the stationary type α has screen leakage due to insufficient sensitivity of the existing means in the inspection process.

Chinese patent application 201510618319.5 entitled "method for measuring ratio of alpha to beta globin chains of hemoglobin" and application thereof discloses that a mass spectrometer is used for detecting a hemoglobin cleavage fragment as a marker peptide fragment to infer the ratio of alpha globin chains to beta globin chains of hemoglobin, and the beta thalassemia is identified. The method obtains the peak area ratio of fragment ion peaks by marking the cracking fragments of alpha and beta globin chains by isotopes, and the peak area ratio is used as judgment basis. Although the method adopts mass spectrometry technology for detection, the actual method is to infer the relative content ratio among globin chains by detecting the proportional relation of the hemoglobin cleavage peptide fragments, and low-abundance globin chains (such as chains) cannot be analyzed simultaneously, so that the high-incidence alpha-thalassemia in China cannot be screened simultaneously.

Chinese patent application 201910945988.1, entitled "characteristic protein marker composition for mass spectrometric diagnosis of thalassemia and diagnostic product thereof" discloses the identification of thalassemia by detecting the relative content of hemoglobin alpha, beta, gamma globin chains using MALDI-TOF mass spectrometer. The method comprises the steps of carrying out relative quantification on a target globin chain and an internal standard substance (an internal standard protein standard substance apomyoglobin, m/z is 169952), respectively determining the content of different globin chains of a normal population relative to the internal standard substance and the content of the globin chain of a thalassemia patient relative to the internal standard substance, determining the up-regulation and down-regulation changes of alpha, beta and gamma globin chains, and taking the up-regulation and down-regulation changes as judgment basis. Although the method adopts MALDI-TOF mass spectrometry technology for detection, the actual method is to detect the content change of different globin chains of hemoglobin.

Disclosure of Invention

The invention aims to provide a method and a device for screening thalassemia based on a time-of-flight mass spectrometry technology, which are used for solving at least one problem in the prior art.

In order to achieve the purpose, the invention adopts the following technical scheme:

a first aspect of the present invention relates to a method for screening thalassemia, comprising

Receiving hemoglobin spectrogram data of a sample to be detected of a detected person;

Optionally, said determining whether the subject has thalassemia comprises determining whether the subject has thalassemia based on a correlation of the ratio between the peak areas of the globin chain and the beta globin chain, the ratio between the peak areas of the globin chain and the alpha globin chain, and the ratio between the peak areas of the beta globin chain and the alpha globin chain

Optionally, the first threshold is 11.0% ± 0.5%, the second threshold is 9.5% ± 0.5%, and the third threshold is 125.0% ± 0.5%.

Optionally, before receiving hemoglobin spectral data of a test sample of a subject, the method further comprises

Preparing a sample to be detected of an examinee;

and dropwise adding a sample to be detected of the detected person onto a target plate of the time-of-flight mass spectrometer by using a micropipette.

And collecting a sample to be detected of a detected person by using a time-of-flight mass spectrometer to obtain hemoglobin spectrogram data of the sample to be detected.

A second aspect of the invention relates to a computing device comprising a processor and a memory, the memory having stored therein a program that when executed by the processor effects:

receiving hemoglobin spectrogram data of a sample to be detected of a detected person;

Optionally, the first threshold is 11.0% ± 0.5%, the second threshold is 9.5% ± 0.5%, and the third threshold is 125.0% ± 0.5%.

A third aspect of the present invention relates to a storage medium storing a program that, when executed, realizes:

receiving hemoglobin spectrogram data of a sample to be detected of a detected person;

Optionally, the first threshold is 11.0% ± 0.5%, the second threshold is 9.5% ± 0.5%, and the third threshold is 125.0% ± 0.5%.

A fourth aspect of the present invention relates to a thalassemia screening apparatus, comprising

the computing device of the second aspect of the invention.

A fifth aspect of the present invention relates to a thalassemia screening system, comprising

The apparatus of the fourth aspect of the invention;

and the display is used for displaying the judgment result.

Optionally, the system further comprises

And the micropipettor is used for dripping a sample to be detected of the detected person onto a target plate of the mass spectrometer.

The invention has the following beneficial effects:

the invention uses matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) to qualitatively analyze the thalassemia by observing hemoglobin globin chains and combining quantitative calculation of software. A large number of sample analysis statistics show that a stable proportional relation exists between different globin chain contents of hemoglobin of healthy people, and the proportional relation can be obviously changed for thalassemia patients. Based on the characteristics of the new generation of MALDI-TOF MS that the quantitative reproducibility is good, the accurate analysis of the relative content of different hemoglobin chains in whole blood can be realized, and a perfect Mediterranean anemia screening method, device and system are established, so that the problems of complex flow, low accuracy and easy screen leakage of the Mediterranean anemia screening are solved. Based on the time-of-flight mass spectrometry protein analysis technology, an analysis object is changed from a hemoglobin tetramer into each specific globin chain, the specific change of each globin chain can be directly analyzed, and the specificity is stronger. In addition, the method only needs one detection, the sample pretreatment process is simple and quick, the consumption of reagent consumables is low, and the detection flux is high. The detection result is not easily influenced by laboratory conditions, the standard unification is more easily realized, and the kit is expected to be applied to large-scale clinical screening of thalassemia.

Compared with the existing electrophoresis method, the method greatly shortens the time of sample pretreatment, and effectively solves the problems of low accuracy, low detection flux, poor specificity and sensitivity and the like existing in the existing method for screening the thalassemia.

Although the chinese patent application 201510618319.5 adopts mass spectrometry for detection, the actual method is to infer the relative content ratio between globin chains by detecting the proportional relationship of the peptide fragments of hemoglobin cleavage, which is different from the method of the present invention (i.e. directly analyzing the relative ratio relationship between α, β and globin chains). The method related by the patent can only analyze high abundance globin chains, cannot analyze low abundance globin chains (such as chains) at the same time, and cannot screen high-incidence alpha-thalassemia in China at the same time.

Compared with the Chinese patent application 201910945988.1, although the method adopts MALDI-TOF mass spectrometry technology for detection, the actual method is to detect the content change of different globin chains of hemoglobin relative to the reference object after adding the reference object, the result is easily influenced by the self deviation of the reference object and unknown interference between the reference object and the sample, and the method adopts the relative proportion relation of the globin chains in human blood (namely directly analyzing the relative proportion relation of alpha, beta and globin chains) without introducing external substances, so that other interference factors are not needed, the result specificity is higher, and the detection is more accurate.

Drawings

The following describes embodiments of the present invention in further detail with reference to the accompanying drawings;

FIG. 1 is a screenshot of a hemoglobin spectrum of a normal individual obtained by the analysis program of the present invention.

Fig. 2 is a display screenshot of a hemoglobin spectrum of a beta thalassemia patient obtained by the analysis procedure of the present invention.

Fig. 3 is a display screen shot of a hemoglobin spectrum of an α thalassemia patient obtained by the analysis program of the present invention.

Fig. 4 shows a thalassemia screening method according to an embodiment of the present invention.

Fig. 5 shows a quantitative results display screenshot of a subject who is a beta thalassemia patient according to an embodiment of the present invention.

Fig. 6 shows a quantitative results display screenshot of a subject who is an α thalassemia patient according to an embodiment of the present invention.

FIG. 7 illustrates a computer system architecture diagram suitable for use in implementing the screening method of an embodiment of the present invention.

Detailed Description

In order to more clearly illustrate the invention, the invention is further described below with reference to preferred embodiments and the accompanying drawings. Similar parts in the figures are denoted by the same reference numerals. It is to be understood by persons skilled in the art that the following detailed description is illustrative and not restrictive, and is not to be taken as limiting the scope of the invention.

Through a large number of sample analysis statistics of the inventor, a stable proportional relation exists between different globin chain contents of hemoglobin of healthy people, and the proportional relation is obviously changed for thalassemia patients. The specific process is as follows:

normal population sample analysis

(1) Preparing a sample: 50 whole blood samples of normal population are available, and 50 samples are from Chinese academy of sciences sample bank. Mixing the 50 normal population samples with tertiary water according to the volume ratio of 1:200 to obtain primary diluent, and then mixing SA matrix liquid with the primary diluent according to the volume ratio of 1:10 to obtain a sample to be detected.

(2) Preparing a target plate: and (3) dropwise adding the 50 samples to be detected onto a target plate matched with the flight time mass spectrometer by using a micropipette, repeatedly dotting 2 target holes on each sample, and naturally drying and crystallizing the samples after dropwise adding.

(3) And (3) placing the dried target plate on a flight time mass spectrum for collection to obtain mass spectrum data containing all globin chains and variants thereof. FIG. 1 is a screenshot of a hemoglobin spectrum of a normal individual obtained by the analysis program of the present invention. In the spectrogram, an m/z-15127 Da peak is an alpha globin chain mass spectrum peak, an m/z-15868 Da peak is a beta globin chain mass spectrum peak, and an m/z-15924 Da peak is a globin chain mass spectrum peak.

(4) Inputting the mass spectrogram data into the program of the invention, and calculating the relative abundance ratio of each globin chain in the whole blood sample of the normal population.

β floorAnalysis of samples from patients with thalassemia

(1) Preparing a sample: there are 100 whole blood samples of patients with beta thalassemia, 100 samples from the sample bank of the Chinese academy of sciences. The whole blood samples of 100 cases of beta thalassemia patients are mixed with tertiary water according to the volume ratio of 1:200 to obtain primary diluent, and then SA matrix solution is mixed with the primary diluent according to the volume ratio of 1:10 to obtain a sample to be detected.

(2) Preparing a target plate: and (3) dropwise adding the 100 samples to be detected onto a target plate matched with the flight time mass spectrometer by using a micropipette, repeatedly dotting 2 target holes on each sample, and naturally drying and crystallizing the sample after dropwise adding.

(3) And (3) placing the dried target plate on a flight time mass spectrum for collection to obtain mass spectrum data containing all globin chains and variants thereof. FIG. 2 is a hemoglobin spectrum of a beta thalassemia patient obtained by the analysis procedure of the present invention. In the spectrogram, an m/z-15127 Da peak is an alpha globin chain mass spectrum peak, an m/z-15868 Da peak is a beta globin chain mass spectrum peak, and an m/z-15924 Da peak is a globin chain mass spectrum peak. From the mass spectrogram, the abundance of the beta globin chain is obviously lower than that of the alpha globin chain, and the abundance of the globin chain relative to the beta globin chain is obviously higher than that of a healthy population sample.

(4) Inputting the mass spectrogram data into the program of the invention, and calculating the relative abundance ratio of each globin chain in the whole blood sample of the patient with beta thalassemia.

α thalassemia patient sample analysis

(1) Preparing a sample: there are 100 whole blood samples from patients with alpha thalassemia, 100 samples from the sample bank of the Chinese academy of sciences. The whole blood samples of 100 cases of alpha thalassemia patients are mixed with tertiary water according to the volume ratio of 1:200 to obtain primary diluent, and then SA matrix solution is mixed with the primary diluent according to the volume ratio of 1:10 to obtain a sample to be detected.

(3) And (3) placing the dried target plate on a flight time mass spectrum for collection to obtain mass spectrum data containing all globin chains and variants thereof. Fig. 3 is a display screen shot of a hemoglobin spectrum of an α thalassemia patient obtained by the analysis program of the present invention. In the spectrogram, an m/z-15127 Da peak is an alpha globin chain mass spectrum peak, an m/z-15868 Da peak is a beta globin chain mass spectrum peak, and an m/z-15924 Da peak is a globin chain mass spectrum peak. From the mass spectra, it was found that the alpha globin chain abundance was significantly lower than the beta globin chain abundance.

(4) Inputting the mass spectrogram data into the program of the invention, and calculating the relative abundance ratio of each globin chain in the whole blood sample of the alpha thalassemia patient.

According to the relative abundance relation of various globin chains in different types of whole blood samples obtained by the three groups of samples, the algorithm integrates peak areas based on statistical analysis and calculates the relative peak area ratio of different globin chains to obtain the significant difference between the beta/alpha,/beta ratios in normal population and thalassemia patients, and then performs regression analysis according to the distribution condition of the sample ratio of each type to obtain the cut-off point (Cutoff) values of the three globin chains between the thalassemia patients and the healthy population, namely a first threshold value corresponding to/beta, a second threshold value corresponding to/alpha and a third threshold value corresponding to beta/alpha. The Cutoff value of how to statistically obtain data by regression analysis is common knowledge of those skilled in the art.

The inventors have found that differences in the number of samples sampled may cause the threshold to vary slightly, and given that the method of the present patent is a screening instrument, the threshold may be fine-tuned to optimize the sensitivity of the detection. For this purpose, the threshold value referred to in the present invention may be a range of values, namely: the center value ± deviation, for example, the first threshold value ═ a first center value ± first deviation.

Through analysis, if the peak area ratio of the globin chain to the beta globin chain is larger than a first threshold, the peak area ratio of the globin chain to the alpha globin chain is larger than a second threshold, and the peak area ratio of the beta globin chain to the alpha globin chain is smaller than a third threshold, the detected person is judged to be beta thalassemia; if the ratio of the globin chain peak area to the alpha globin chain peak area is less than the second threshold or the ratio of the beta globin chain peak area to the alpha globin chain peak area is greater than the third threshold, determining that the detected person is alpha thalassemia; if the ratio of the peak area of the globin chain to the peak area of the beta globin chain is less than the first threshold, the ratio of the peak area of the globin chain to the peak area of the alpha globin chain is greater than the second threshold, and the ratio of the peak area of the beta globin chain to the peak area of the alpha globin chain is less than the third threshold, judging that the detected person is normal; if none of the three conditions is true, the determination is suspected, and the test is performed again or other auxiliary means are adopted for confirmation.

In the explanation of the threshold values described above, for example, "> first threshold value" means "> (first central value + first deviation)"; "< third threshold" means "< (third central value-third deviation").

According to the rule, when the algorithm detects that the numerical value is in the range of [ central value-deviation, central value + deviation ], the suspected sample is judged. For example, if the peak area ratio of the globin chain to the beta globin chain falls into [ first center value-first deviation, first center value + first deviation ], the peak area ratio of the globin chain peak area to the alpha globin chain peak area > a second threshold, and the peak area ratio of the beta globin chain peak area to the alpha globin chain peak area < a third threshold, the suspected sample is determined.

Specifically, as further analysis of the β thalassemia patient samples of fig. 2, the peak area integral calculation by the software revealed that the relative ratio of globin chains to β globin chains in the β thalassemia patient samples was > 11%, the relative ratio of globin chains to α globin chains was > 9.5%, and the relative ratio of β globin chains to α globin chains was < 125.0%. The number of samples is increased or decreased, and these values are slightly changed.

Similarly, as further analysis of the α thalassemia patient samples of fig. 3, the peak area integral calculation by the software revealed that the relative ratio of β globin chain to α globin chain in the α thalassemia patient samples was > 125.0%. The number of samples is increased or decreased, and the value is slightly changed.

Similarly, as the normal population sample of fig. 1 is further analyzed, the peak area integral calculation by the software shows that the relative ratio of the globin chain to the beta globin chain in the normal population sample is less than 11.0%, the relative ratio of the globin chain to the alpha globin chain is greater than 9.5%, and the relative ratio of the beta globin chain to the alpha globin chain is less than 125.0%.

Therefore, more preferably, in order to avoid missing detection, the present invention uses the range values of the distribution of the ratio of each type of sample obtained at different sample numbers, i.e. the first threshold value is 11.0% ± 0.5%, the second threshold value is 9.5% ± 0.5%, and the third threshold value is 125.0% ± 0.5%.

In conclusion, the inventor finds out the statistical rules through the statistical analysis of a large number of samples and can be used as a judgment standard for screening thalassemia patients.

Thus, as shown in fig. 4, the present invention provides a method for screening thalassemia, comprising

S101, receiving hemoglobin spectrogram data of a sample to be detected of a detected person;

s103, integrating peak areas of an alpha globin chain, a beta globin chain and a globin chain in the hemoglobin spectrogram data, and respectively calculating a ratio between peak areas of the globin chain and the beta globin chain, a ratio between peak areas of the globin chain and the alpha globin chain and a ratio between peak areas of the beta globin chain and the alpha globin chain;

s105, determining whether the detected person suffers from thalassemia or not according to the correlation of the ratio of the peak areas of the globin chain and the beta globin chain, the ratio of the peak areas of the globin chain and the alpha globin chain and the ratio of the peak areas of the beta globin chain and the alpha globin chain.

The invention uses matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) to qualitatively analyze the thalassemia by observing hemoglobin globin chains and combining quantitative calculation of software. A large number of sample analysis statistics show that a stable proportional relation exists between different globin chain contents of hemoglobin of healthy people, and the proportional relation can be obviously changed for thalassemia patients. Based on the characteristics of the new generation of MALDI-TOF MS that the quantitative reproducibility is good, the accurate analysis of the relative content of different hemoglobin chains in whole blood can be realized, and a perfect Mediterranean anemia screening method, device and system are established, so that the problems of complex flow, low accuracy and easy screen leakage of the Mediterranean anemia screening are solved. Based on the time-of-flight mass spectrometry protein analysis technology, an analysis object is changed from a hemoglobin tetramer into each specific globin chain, the specific change of each globin chain can be directly analyzed, and the specificity is stronger. In addition, the method only needs one detection, the sample pretreatment process is simple and quick, the consumption of reagent consumables is low, and the detection flux is high. The detection result is not easily influenced by laboratory conditions, the standard unification is more easily realized, and the kit is expected to be applied to large-scale clinical screening of thalassemia.

Optionally, the first threshold is 11.0% ± 0.5%, the second threshold is 9.5% ± 0.5%, and the third threshold is 125.0% ± 0.5%.

Next, the statistical law is verified.

In one particular embodiment:

preparing a sample: a whole blood sample of a beta thalassemia subject A is taken and is from a sample bank of Chinese academy of sciences. The sample was mixed with pure water at a volume ratio of 1:200 to obtain a primary dilution. And mixing the primary diluent with the SA matrix solution according to the volume ratio of 1:10, and uniformly mixing by vortex to obtain the sample to be detected.

Preparing a target plate: and (3) dropwise adding the sample A to be detected onto a target plate matched with the flight time mass spectrum by using a micropipette, and naturally airing the sample A, wherein each sample is parallel to 2 target holes.

And (3) scanning the dried target plate on a flight time mass spectrum to obtain a mass spectrogram containing different globin chains.

A screenshot of the quantitative results for the subject is shown in figure 5. As can be seen from the graph, the values of the ratios of β/α,/β of the sample of group A2 were 58.3%, 9.8% and 16.9%, respectively, the values of β/α,/β of the sample of group B2 were 66.4%, 10.4% and 15.6%, respectively, and the values of β/α,/β of the sample of group C2 were 69.1%, 9.5% and 13.8%, respectively, and the subject was beta thalassemia according to the above criteria. The correctness of the judgment standard is indicated according to the actual situation of the sample.

Similarly, α thalassemia samples were prepared, and a screenshot showing the quantitative results of the subjects is shown in fig. 6. As can be seen from the figure, the values of β/α,/β of the samples of the first group were 137.6%, 13.8% and 19.0%, respectively, and the values of β/α,/β of the samples of the second group were 145.1%, 13.8% and 20.0%, respectively, and according to the above-mentioned criteria, the ratio of the peak area of the β -globin chain to the peak area of the α -globin chain was satisfied with > 125.0% (although the ratio of the peak area of the globin chain to the peak area of the α -globin chain was not satisfied with < 9.5%), and the subject was α -thalassemia. The correctness of the judgment standard is indicated according to the actual situation of the sample.

Optionally, before receiving hemoglobin spectral data of a test sample of a subject, the method further comprises

Preparing a sample to be detected of an examinee;

wherein the preparation method is similar to that described previously.

And dropwise adding a sample to be detected of the detected person onto a target plate of the time-of-flight mass spectrometer by using a micropipette.

And collecting a sample to be detected of a detected person by using a time-of-flight mass spectrometer to obtain hemoglobin spectrogram data of the sample to be detected.

The invention provides a computing device comprising a processor which, when executing a program, carries out the method steps shown in figure 4.

In a specific example, as shown in fig. 7, a computer system suitable for implementing the screening method provided by the present embodiment includes a Central Processing Unit (CPU), which can execute the method according to a program stored in a Read Only Memory (ROM) or a program loaded from a storage portion into a Random Access Memory (RAM), for example, an application program implementing the recruitment method or when executing the program. The CPU, ROM, and RAM are connected thereto via a bus. An input/output (I/O) interface is also connected to the bus.

An input section including a keyboard, a mouse, and the like; an output section including a speaker and the like such as a Liquid Crystal Display (LCD); a storage section including a hard disk and the like; and a communication section including a network interface card such as a LAN card, a modem, or the like. The communication section performs communication processing via a network such as the internet. The drive is also connected to the I/O interface as needed. A removable medium such as a magnetic disk, an optical disk, a magneto-optical disk, a semiconductor memory, or the like is mounted on the drive as necessary, so that a computer program read out therefrom is mounted into the storage section as necessary.

In particular, the processes described in the above flowcharts may be implemented as computer software programs according to the present embodiment. For example, the present embodiments include a computer program product comprising a computer program tangibly embodied on a computer-readable medium, the computer program comprising program code for performing the method illustrated in the flow chart. In such an embodiment, the computer program may be downloaded and installed from a network via the communication section, and/or installed from a removable medium.

The flowchart and schematic diagrams in the figures illustrate the architecture, functionality, and operation of possible implementations of systems, methods and computer program products according to the present embodiments. In this regard, each block in the flowchart or schematic diagrams may represent a module, segment, or portion of code, which comprises one or more executable instructions for implementing the specified logical function(s). It should also be noted that, in some alternative implementations, the functions noted in the block may occur out of the order noted in the figures. For example, two blocks shown in succession may, in fact, be executed substantially concurrently, or the blocks may sometimes be executed in the reverse order, depending upon the functionality involved. It will also be noted that each block of the schematic and/or flowchart illustration, and combinations of blocks in the schematic and/or flowchart illustration, can be implemented by special purpose hardware-based systems which perform the specified functions or acts, or combinations of special purpose hardware and computer instructions.

The modules referred to in the embodiments described may be implemented by means of software. The modules described may also be provided in a processor.

On the other hand, the present embodiment also provides a nonvolatile computer storage medium, which may be the nonvolatile computer storage medium included in the apparatus in the foregoing embodiment, or may be a nonvolatile computer storage medium that exists separately and is not assembled into a terminal. The non-volatile computer storage medium stores one or more programs that, when executed by an apparatus, cause the apparatus to perform the screening method of the present application.

The invention also provides a mediterranean anemia screening device, which comprises

The invention also provides a mediterranean anemia screening system, which comprises

The thalassemia screening device described above; and

and the display is used for displaying the judgment result.

Specifically, the result report is, for example, displayed as "β -thalassemia", "α -thalassemia", "normal", and "suspected".

Optionally, the system further comprises

And the micropipettor is used for dripping a sample to be detected of the detected person onto a target plate of the mass spectrometer.

It is to be noted that, in the description of the present invention, relational terms such as first and second, and the like are used solely to distinguish one entity or action from another entity or action without necessarily requiring or implying any actual such relationship or order between such entities or actions. Also, the terms "comprises," "comprising," or any other variation thereof, are intended to cover a non-exclusive inclusion.

It should be understood that the above-mentioned embodiments of the present invention are only examples for clearly illustrating the present invention, and are not intended to limit the embodiments of the present invention, and it will be obvious to those skilled in the art that other variations and modifications can be made on the basis of the above description, and all embodiments cannot be exhaustive, and all obvious variations and modifications belonging to the technical scheme of the present invention are within the protection scope of the present invention.

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Computing equipment, storage medium and thalassemia screening device and system

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