Storage and inspection method, system and equipment for biological samples and storage medium

Abstract

The invention relates to the technical field of biological detection materials, in particular to a biological detection material storage and inspection method, system and device and a storage medium, the method comprises the steps that partition information of a target detection material box is acquired, and the partition information comprises target detection material information of all partitions of the target detection material box; according to the target inspection material information, determining the predicted inactivation time of the target inspection material and the predicted delivery time of the target inspection material to a first target inspection point; if the predicted arrival time exceeds the predicted inactivation time, obtaining alternative inspection target point information of the target inspection material; and according to the alternative inspection target point information, determining an alternative inspection target point closest to the target inspection material box as a second target inspection point. The method has the beneficial effect of ensuring the activity of the biological sample when the biological sample is sent to a related detection point.

Description

Technical Field

[0001] The present application relates to the technical field of biological samples, and in particular to a method, system, device and storage medium for storing and sending biological samples for inspection. Background Art

[0002] A biological specimen box is a device specially used to collect, store and transport biological specimens. These biological specimens may include human biological samples such as blood, saliva, semen stains, urine, and feces, or samples of biological species such as plants, animals or microorganisms. In the actual transportation process of biological specimens, due to factors such as the characteristics of different specimens, collection time, and storage environment, there may be cases where biological specimens are inactivated before they are delivered to relevant testing points.

[0003] Therefore, how to ensure that biological samples remain active when they are delivered to relevant testing points is a technical problem that needs to be solved urgently. Summary of the invention

[0004] The embodiments of the present application provide a method, system, device and storage medium for storing and delivering biological samples, which can achieve the beneficial effect of ensuring that the biological samples remain active when delivered to relevant testing points.

[0005] The first aspect of the present application provides a method for storing and sending biological samples for inspection: A method for storing and sending biological samples for inspection, applied to a biological sample box, the method comprising: Acquire partition information of a target material box, wherein the partition information includes target material information of each partition of the target material box; Determine, based on the target sample information, an estimated inactivation time of the target sample and an estimated delivery time of the target sample to the first target delivery point; If the estimated delivery time exceeds the estimated inactivation time, obtaining the alternative delivery target point information of the target sample; According to the information of the candidate inspection target point, the candidate inspection target point closest to the target inspection material box is determined as the second target inspection point.

[0006] By adopting the above technical solution, based on the target sample information, it is determined whether the target sample may have been inactivated when it is delivered to the target inspection point, and the potentially inactivated biological sample is sent to an alternative inspection point for inspection, thereby ensuring that the biological sample remains active when it is delivered to the relevant inspection point.

[0007] Optionally, the method further includes: If the absolute value of the time difference between the estimated delivery time and the estimated inactivation time is less than a first preset threshold, obtaining a preset target sample sorting ratio; According to the target sample inspection ratio, a first portion of the target sample to be sent to the first target inspection point and a second portion of the target sample to be sent to the second target inspection point are determined.

[0008] By adopting the above technical solution, target samples that may still be active when delivered to the original inspection point are screened out according to the expected delivery time and the expected inactivation time. Part of them are transported to the original inspection point, and the other part is transported to the alternative inspection point. If it is subsequently determined that the target samples are still active when delivered to the original inspection point, they are tested at the original inspection point, thereby reducing the testing volume at the alternative inspection point.

[0009] Optionally, the method further includes: Determining the estimated inactivation time of the target sample in each partition of the target sample box according to the partition information; According to the estimated inactivation time of the target samples in each partition, target samples whose estimated inactivation time is in the same preset estimated inactivation time period are determined as similar inactivation samples; If the ratio of the number of similar inactivated samples to the total number of samples in the target sample box reaches a preset ratio threshold, the target sample box is controlled to send a first prompt message to the target user.

[0010] By adopting the above technical solution, biological samples with similar expected inactivation times can be stored in the same biological sample box as much as possible, so that when the delivery point needs to be adjusted during subsequent transportation, the entire box can be transported to an alternative delivery point without having to take out the samples and re-store them, thereby facilitating the transportation of the samples.

[0011] Optionally, before the step of obtaining the partition information of the target material inspection box, the method further includes: Obtain target sample input information entered by the target user; According to the input information of the target sample, determine whether there is a risk of sample contamination; If the sample contamination risk exists, a partition storage plan is generated according to the target sample corresponding to the sample contamination risk.

[0012] By adopting the above technical solution, according to the target sample input information, it is determined whether there is a risk of cross contamination among multiple biological samples stored in the same biological sample box, and a partition storage plan is generated according to the contamination risk, so as to allocate storage as much as possible and keep biological samples that are prone to cross contamination away from each other, thereby avoiding cross contamination.

[0013] Optionally, the method further includes: Determine the reason for sending the target sample for inspection according to the input information of the target sample; Determine the sample requirement information based on the reason for the sample submission; If the target sample information does not meet the sample requirement information, a second prompt message is sent to the target user.

[0014] By adopting the above technical solution, the list of biological samples required for inspection is determined according to the corresponding purposes of the biological samples, thereby avoiding unnecessary trouble caused by wrong storage or missing storage of biological samples when submitting for inspection.

[0015] Optionally, the method further includes: According to the target sample information, obtaining matching parameter information of the target sample; According to the matching parameter information, the storage parameters of the partition where the target sample is located are adjusted to the matching parameters.

[0016] By adopting the above technical solution, according to the characteristics of different biological samples in each partition, the temperature, humidity and other parameters of each partition are adjusted to be matching parameters suitable for the corresponding biological samples, thereby ensuring the stability and activity of the biological samples during storage and transportation, and making the estimated inactivation time more accurate.

[0017] Optionally, the method further includes: Acquire the storage parameter information of each partition of the target material box; A storage parameter report of the target sample box is generated according to the storage parameter information, and the storage parameter report is sent to the target user.

[0018] By adopting the above technical solution, relevant information such as the collection time, storage parameters, and expected inactivation time of the biological samples during the storage and transportation process are sent to the corresponding target users, so that the target users can understand the status of each biological sample in the biological sample box.

[0019] The second aspect of the present application provides a biological sample storage and inspection system, comprising: A partition information acquisition module, used to acquire partition information of a target material box, wherein the partition information includes target material information of each partition of the target material box; A time estimation module, used to determine the estimated inactivation time of the target sample and the estimated delivery time of the target sample to the first target delivery point according to the target sample information; An alternative inspection point acquisition module is used to obtain the alternative inspection target point information of the target inspection material if the estimated delivery time exceeds the estimated inactivation time; The inspection point adjustment module is used to determine the alternative inspection target point closest to the target inspection material box as the second target inspection point according to the alternative inspection target point information.

[0020] The third aspect of the present application provides a device, including a memory and a processor, wherein the memory stores a computer program that can be loaded by the processor and execute the above-mentioned method for storing and submitting biological samples for inspection.

[0021] A fourth aspect of the present application provides a storage medium storing a computer program that can be loaded by a processor and execute the above-mentioned method for storing and submitting biological samples for inspection.

[0022] In summary, the present application includes at least one of the following beneficial effects: 1. Since the original target inspection point can carry a larger amount of tests and more types of tests, the biological samples will be planned to be transported to the original target inspection point first. At the same time, it will be determined whether the target samples may have been inactivated when they arrive at the target inspection point, and the corresponding biological samples that may have been inactivated will be sent to the alternative inspection point for inspection, so as to ensure that the biological samples remain active when they arrive at the relevant inspection point.

[0023] 2. Based on the estimated delivery time and the estimated inactivation time, the target samples that may still be active when delivered to the original inspection point are screened out, and part of them are transported to the original inspection point, and the other part is transported to the alternative inspection point. If it is subsequently determined that the target samples are still active when delivered to the original inspection point, they will be tested at the original inspection point, thereby reducing the testing volume at the alternative inspection point.

[0024] 3. According to the characteristics of different biological samples in each partition, the temperature, humidity and other parameters of each partition are adjusted to match the corresponding biological samples, so as to ensure the stability and activity of the biological samples during storage and transportation, and make the estimated inactivation time more accurate. BRIEF DESCRIPTION OF THE DRAWINGS

[0025] Figure 1 It is a schematic diagram of the process of storing and sending biological samples for inspection provided in an embodiment of the present application; Figure 2 It is a virtual structural diagram of the biological sample storage and inspection system provided in this application. DETAILED DESCRIPTION

[0026] The following examples will help those skilled in the art to further understand the effects of the present application, but are not intended to limit the present application in any form. It should be noted that, for those of ordinary skill in the art, several modifications and improvements may be made without departing from the concept of the present application. These all fall within the scope of protection of the present application.

[0027] In the following description, specific details such as specific system structures, technologies, etc. are provided for the purpose of illustration rather than limitation, so as to provide a thorough understanding of the embodiments of the present application. However, it should be clear to those skilled in the art that the present application may also be implemented in other embodiments without these specific details. In other cases, detailed descriptions of well-known systems, devices, circuits, and methods are omitted to prevent unnecessary details from obstructing the description of the present application.

[0028] It should be understood that when used in the present specification and the appended claims, the term "comprising" indicates the presence of described features, wholes, steps, operations, elements and / or components, but does not exclude the presence or addition of one or more other features, wholes, steps, operations, elements, components and / or combinations thereof.

[0029] It should also be understood that the term “and / or” used in the specification and appended claims refers to any and all possible combinations of one or more of the associated listed items, and includes these combinations.

[0030] As used in the specification and appended claims of this application, the term "if" can be interpreted as "when" or "uponce" or "in response to determining" or "in response to detecting", depending on the context. Similarly, the phrase "if it is determined" or "if [described condition or event] is detected" can be interpreted as meaning "uponce it is determined" or "in response to determining" or "uponce [described condition or event] is detected" or "in response to detecting [described condition or event]", depending on the context.

[0031] In addition, in the description of the present application specification and the appended claims, the terms "first", "second", "third", etc. are only used to distinguish the descriptions and cannot be understood as indicating or implying relative importance.

[0032] References to "one embodiment" or "some embodiments" etc. described in the specification of this application mean that one or more embodiments of the present application include specific features, structures or characteristics described in conjunction with the embodiment. Therefore, the statements "in one embodiment", "in some embodiments", "in some other embodiments", "in some other embodiments", etc. that appear in different places in this specification do not necessarily refer to the same embodiment, but mean "one or more but not all embodiments", unless otherwise specifically emphasized in other ways. The terms "including", "comprising", "having" and their variations all mean "including but not limited to", unless otherwise specifically emphasized in other ways.

[0033] In order to make the purpose, technical solutions and advantages of the present application clearer, the storage and delivery method of biological samples of the present application is explained below from the perspective of the storage and delivery device of biological samples. The storage and delivery device of biological samples can be an electronic device, such as a mobile phone terminal, a computer terminal and other devices.

[0034] The present application is further described in detail below in conjunction with the accompanying drawings.

[0035] Reference Figure 1 , Figure 1 : is a flow chart of a method for storing and submitting biological samples provided in an embodiment of the present application, the method comprising the following steps: In step S1, the partition information of the target sample box is obtained, and the partition information includes the target sample information of each partition of the target sample box.

[0036] Specifically, the target sample box can be equipped with an integrated storage area for classified storage of a variety of different biological samples. The partitions are independent of each other due to their sealing, and theoretically will not interfere with each other. The integrated storage area can be customized and adjusted according to the actual needs of the target user to meet the actual use needs. In the integrated storage area, the target sample information corresponding to the different biological samples stored in each partition can be entered by the collector. The target user can enter the information and synchronize it to the target sample box through terminal control, voice entry, text input and other methods. The entered target sample information includes but is not limited to the sample name, collection time, first target inspection point, etc.

[0037] More specifically, since the target sample box provided by the present application can have an integrated storage area to store multiple samples of the same type but from different sources, or the same type but at different collection times, in order to prevent cross-contamination and cross-contamination, samples that are easily contaminated with each other should be stored in different sample boxes as much as possible, or the distance between the storage partitions should be increased so that samples that are easily cross-contaminated or contaminated are far away from each other. Therefore, a partitioning scheme can also be recommended based on the entered target sample information, which is specifically explained below: Obtain target sample input information entered by the target user; According to the input information of the target sample, determine whether there is a risk of sample contamination; If the sample contamination risk exists, a partition storage plan is generated according to the target sample corresponding to the sample contamination risk.

[0038] Specifically, after the target user enters the target sample information, the target sample type will be included. Different types of biological samples will undergo thermal motion of molecules when stored. On the one hand, the sealing of the sample box may be reduced in actual use, and on the other hand, cross contamination may be caused by improper operation during the storage or retrieval process. Therefore, after the target user enters the information, data related to the possible impacts between all biological samples stored in the target sample box can be obtained. This data can be obtained from a relevant information database, which can include experience summarized from actual operations, or conclusions drawn from the impacts that theories will produce.

[0039] More specifically, the corresponding partition storage plan is generated according to the database. The partition storage plan should determine the biological samples that are prone to cross-contamination or cross-contamination, and keep the physical distance of the storage partitions as far as possible. In addition, when entering information in the partitions, due to the needs of actual use, the biological samples that need to be collected can also be determined according to the target sample entry information to avoid missed collection and storage. The following is a specific explanation: Determine the reason for sending the target sample for inspection according to the input information of the target sample; Determine the sample requirement information based on the reason for the sample submission; If the target sample information does not meet the sample requirement information, a second prompt message is sent to the target user.

[0040] Specifically, the target sample input information entered by the target user may include the reasons for the inspection corresponding to the stored biological samples in each partition. The reason for inspection is the purpose of the biological samples stored and sent for inspection. This purpose includes but is not limited to storage backup, source analysis, etc. According to the different uses of biological samples, the necessary samples are also different. Therefore, this application will also obtain the sample demand information based on the reason for inspection, and judge based on the currently entered biological samples to determine whether the biological samples that have been collected and stored meet the sample demand information. If not, a second prompt message will be sent to the target user.

[0041] More specifically, the target user may be a collector or a transporter, and the second prompt information may be an error report in the form of a voice message, text display, etc. sent by the terminal. In actual use, the target user can cancel the corresponding error report by adding a remark. For example, if it is determined that sample A, sample B, and sample C are required according to the sample demand information, and due to the actual situation, only sample A or sample B can or needs to be collected, the information remark can be entered through information entry, and the sample box or the terminal connected to the sample box will not report an error due to the lack of sample C when the information remark is obtained.

[0042] Furthermore, after the target user enters the target sample information, biological samples with similar estimated inactivation times can be stored in the same biological sample box as much as possible, so as to facilitate transfer when the subsequent delivery point is changed. The following is a specific explanation: Determining the estimated inactivation time of the target sample in each partition of the target sample box according to the partition information; According to the estimated inactivation time of the target samples in each partition, target samples whose estimated inactivation time is in the same preset estimated inactivation time period are determined as similar inactivation samples; If the ratio of the number of similar inactivated samples to the total number of samples in the target sample box reaches a preset ratio threshold, the target sample box is controlled to send a first prompt message to the target user.

[0043] Specifically, the estimation of the expected inactivation time of the target samples in each partition is the same as the estimated inactivation time estimation method in the following step S2. The preset same expected inactivation time period can be set by the target user or by the manufacturer of the biological sample box. In this application, the number of days is used as the unit. For biological samples that may be inactivated on the same day, corresponding prompt information is sent to recommend the target user to store these similar inactivation samples with similar inactivation times in the same biological sample box.

[0044] More specifically, since similar inactivated samples are stored in the same biological sample box as much as possible, if there are unexpected conditions in the storage environment parameters or actual transportation, biological samples in multiple partitions may face the problem of being difficult to deliver before the expected inactivation time. In this case, the ratio of the number of similar inactivated samples to the total number of samples is used to determine whether to send the entire biological sample box to the nearest inspection point. The preset ratio threshold can be set by the target user through a terminal or other communication method, or by the manufacturer of the biological sample box. The first prompt information can be a voice prompt issued by the sample box, a text prompt on the set display screen, an information prompt on the connected terminal, and other notification methods. After receiving the first prompt information, the target user can transfer the corresponding sample box to be transported to the nearest alternative inspection point.

[0045] In step S2, based on the target sample information, the estimated inactivation time of the target sample and the estimated delivery time of the target sample to the first target delivery point are determined.

[0046] Specifically, the estimated inactivation time can be generated based on multiple dimensions such as the type of sample corresponding to the target sample, the collection time, the state of the collected organism, the storage environment, etc., and the first target delivery point, that is, the target delivery point entered by the target user, and the estimated delivery time can be generated based on a comprehensive estimate of the current positioning information of the target sample box, the planned departure time for delivery, and the estimated transportation time to reach the first target delivery point.

[0047] More specifically, since the estimated inactivation time may be affected by the storage environment, in order to ensure the stability and activity of biological samples during storage and transportation, corresponding adjustments can be made according to the preferred storage environment of different samples, as described below: According to the target sample information, the matching parameter information of the target sample is obtained.

[0048] Specifically, the target sample information may include the type of the target sample, and the corresponding sample type may be a human biological sample such as blood, saliva, semen stains, urine, feces, etc., or a sample of a biological species such as plants, animals or microorganisms. The matching parameter information may be retrieved from a database, and for different samples, the preferred storage temperature, humidity, etc. in the database are correspondingly retrieved as matching parameters.

[0049] According to the matching parameter information, the storage parameters of the partition where the target sample is located are adjusted to the matching parameters.

[0050] Specifically, according to the retrieved matching parameter information, the storage parameters of the corresponding partitions in the target sample box are adjusted accordingly. For example, assuming that partition A stores sample A and partition B stores sample B, the recommended storage temperature for sample A in the database is -10°C, and the recommended storage temperature for sample B is 0°C. Then, through temperature control methods such as refrigerators, the temperature of partition A is adjusted to -10°C, and the temperature of partition B is adjusted to 0°C, so as to extend the storage time of the target sample as much as possible. At the same time, since the storage environment is adjustable, the fluctuation of the estimated inactivation time is also smaller, and the estimated time is more accurate.

[0051] More specifically, in order to facilitate the target users related to collection, storage and transportation to grasp the corresponding biological sample conditions, a corresponding report can also be generated according to the storage parameter information, as described below: Acquire the storage parameter information of each partition of the target material box; A storage parameter report of the target sample box is generated according to the storage parameter information, and the storage parameter report is sent to the target user.

[0052] Specifically, the storage parameter report of the target sample box includes, but is not limited to, the name of the target sample, the collection time, the collection source, the purpose of the sample, the storage time, the parameters used for storage, etc., wherein the storage parameters may include the environmental parameter information of the target sample storage location such as temperature, humidity, and pressure. The storage parameter report can be displayed at any time after the target sample is stored in the target sample box through a communication device or a display screen set on the target sample box. When the target sample is taken out, a corresponding storage report can also be generated to facilitate the inspection personnel to grasp the relevant situation of the target sample and facilitate subsequent analysis and inspection.

[0053] In step S3, if the estimated delivery time exceeds the estimated inactivation time, the alternative delivery target point information of the target sample is obtained.

[0054] Specifically, if the expected delivery time exceeds the expected inactivation time, it means that it may be difficult to correctly analyze the corresponding biological sample according to the originally planned transportation destination. This expected inactivation time can be the estimated time when the biological sample is completely inactivated, or it can be the estimated time when inactivation begins and is partially inactivated. The information of the alternative delivery target point should include the sample-related operations that can be performed by the alternative delivery target point, positioning information, and the amount of samples that can be accepted. This is because the first target delivery point originally planned for transportation is usually a delivery point with complete equipment and stronger execution capabilities, while the alternative delivery point may be a delivery point with insufficient equipment and slightly weaker detection capabilities compared to the first target delivery point. Therefore, it is necessary to determine whether the alternative delivery target point can be used as the second target delivery point in the following step S4 based on the above information.

[0055] More specifically, there may be a situation where the estimated inactivation time is close to the estimated delivery time. Due to the fluctuation of the actual delivery time and the accuracy of the estimate, there may be a situation where the corresponding biological sample is not inactivated when it is actually delivered. In order to reduce the testing volume at the second target delivery point, the biological samples that can be tested at the original delivery point should be tested at the original delivery point. The following is a specific explanation: If the absolute value of the time difference between the estimated delivery time and the estimated inactivation time is less than a first preset threshold, a preset target sample sorting ratio is obtained.

[0056] Specifically, the absolute value of the time difference between the expected delivery time and the expected inactivation time can be set according to the actual needs of the target user in a control terminal or other means that can synchronize data to the target sample box, or it can be set by the manufacturer of the biological sample box. The first preset threshold is set in the same way as the preset target sample sorting ratio.

[0057] According to the target sample inspection ratio, a first portion of the target sample to be sent to the first target inspection point and a second portion of the target sample to be sent to the second target inspection point are determined.

[0058] Specifically, in layman's terms, when it is difficult to determine the activity of the corresponding sample when it actually arrives at the first target inspection point, the corresponding sample is divided into two parts and sent to the first target inspection point and the second target inspection point respectively. The part of the sample that arrives at the second target inspection point first will be stored first, while the activity and transportation conditions of the other part of the sample sent to the first target inspection point are monitored. If, based on the monitoring results, it can be determined that part of the sample sent to the first target inspection point cannot arrive before deactivation, then the second target inspection point will be tested to ensure that at least one test point can obtain the test results; if, based on the monitoring results, it can be determined that part of the sample sent to the first target inspection point can arrive before deactivation, then the first target inspection point will be tested, thereby reducing the amount of testing at the second target inspection point.

[0059] In step S4, according to the candidate inspection target point information, the candidate inspection target point closest to the target inspection material box is determined as the second target inspection point.

[0060] Specifically, the second target inspection point is the alternative inspection target point that is closest to the target inspection material box and can undertake the inspection task of the corresponding inspection material. It can also be determined based on the expected arrival or expected inspection time, and the alternative inspection target point with the earliest expected arrival time or expected inspection time that can undertake the inspection task of the corresponding inspection material is selected as the second target inspection point. After determining the second target inspection point, the target inspection material box can send voice, text and other prompt information to the target user through channels such as the display device set on the inspection material box and the connected device terminal, so that the target user can adjust the transportation destination of the inspection material as soon as possible.

[0061] On the other hand, the present application discloses a storage and inspection system for biological samples, see Figure 2 , Figure 2 This is a virtual structural diagram of a biological sample storage and inspection system provided in the present application, and the biological sample storage and inspection system includes: The partition information acquisition module 100 is used to acquire the partition information of the target material box, wherein the partition information includes the target material information of each partition of the target material box; The time estimation module 200 is used to determine the estimated inactivation time of the target sample and the estimated delivery time of the target sample to the first target delivery point according to the target sample information; The alternative inspection point acquisition module 300 is used to acquire the information of the alternative inspection target point of the target inspection material if the estimated delivery time exceeds the estimated inactivation time; The inspection point adjustment module 400 is used to determine the candidate inspection target point closest to the target inspection material box as the second target inspection point according to the candidate inspection target point information.

[0062] For the specific definition of the storage and delivery system for biological samples, please refer to the definition of the storage and delivery method for biological samples above, which will not be repeated here. Each module in the above-mentioned storage and delivery system for biological samples can be implemented in whole or in part through software, hardware and a combination thereof. The above-mentioned modules can be embedded in or independent of the processor in the computer device in the form of hardware, or can be stored in the memory of the computer device in the form of software, so that the processor can call and execute the operations corresponding to the above modules.

[0063] The technicians in the relevant field can clearly understand that for the convenience and simplicity of description, only the division of the above-mentioned functional units and modules is used as an example for illustration. In practical applications, the above-mentioned function allocation can be completed by different functional units and modules as needed, that is, the internal structure of the device can be divided into different functional units or modules to complete all or part of the functions described above. The functional units and modules in the embodiment can be integrated in a processing unit, or each unit can exist physically separately, or two or more units can be integrated in one unit. The above-mentioned integrated unit can be implemented in the form of hardware or in the form of software functional units. In addition, the specific names of the functional units and modules are only for the convenience of distinguishing each other, and are not used to limit the scope of protection of this application. The specific working process of the units and modules in the above-mentioned system can refer to the corresponding process in the aforementioned method embodiment, which will not be repeated here.

[0064] The method for storing and submitting biological samples provided in the embodiments of the present application can be applied to terminal devices such as electronic devices, computers, wearable devices, vehicle-mounted devices, tablet computers, laptop computers, netbooks, personal digital assistants (PDA), augmented reality (AR) / virtual reality (VR) devices, mobile phones, etc. The embodiments of the present application do not impose any restrictions on the specific types of terminal devices.

[0065] The embodiment of the present application further provides a computer-readable storage medium, which stores a computer program. When the computer program is executed by a processor, the steps in each embodiment of the above method can be implemented.

[0066] An embodiment of the present application provides a computer program product. When the computer program product runs on a mobile terminal, the mobile terminal can implement the steps in each embodiment of the above method when executing the computer program product.

[0067] If the integrated unit is implemented in the form of a software functional unit and sold or used as an independent product, it can be stored in a computer-readable storage medium. Based on this understanding, the present application implements all or part of the processes in the above-mentioned embodiment method, which can be completed by instructing the relevant hardware through a computer program, and the computer program can be stored in a computer-readable storage medium. When the computer program is executed by the processor, the steps of the above-mentioned method embodiments can be implemented. Among them, the computer program includes computer program code, and the computer program code can be in source code form, object code form, executable file or some intermediate form. The computer-readable medium may at least include: any entity or device that can carry the computer program code to the camera / terminal device, recording medium, computer memory, read-only memory (ROM, Read-Only Memory), random access memory (RAM, Random Access Memory), electric carrier signal, telecommunication signal and software distribution medium. For example, a USB flash drive, a mobile hard disk, a magnetic disk or an optical disk. In some jurisdictions, according to legislation and patent practice, computer-readable media cannot be electric carrier signals and telecommunication signals.

[0068] In the above embodiments, the description of each embodiment has its own emphasis. For parts that are not described or recorded in detail in a certain embodiment, reference can be made to the relevant descriptions of other embodiments.

[0069] Those of ordinary skill in the art will appreciate that the units and algorithm steps of each example described in conjunction with the embodiments disclosed herein can be implemented in electronic hardware, or a combination of computer software and electronic hardware. Whether these functions are performed in hardware or software depends on the specific application and design constraints of the technical solution. Professional and technical personnel can use different methods to implement the described functions for each specific application, but such implementation should not be considered to be beyond the scope of this application.

[0070] In the embodiments provided in the present application, it should be understood that the disclosed devices / network equipment and methods can be implemented in other ways. For example, the device / network equipment embodiments described above are only schematic. For example, the division of modules or units is only a logical function division. There may be other division methods in actual implementation, such as multiple units or components can be combined or integrated into another system, or some features can be ignored or not executed. Another point is that the mutual coupling or direct coupling or communication connection shown or discussed can be through some interfaces, indirect coupling or communication connection of devices or units, which can be electrical, mechanical or other forms.

[0071] The units described as separate components may or may not be physically separated, and the components shown as units may or may not be physical units, that is, they may be located in one place or distributed on multiple network units. Some or all of the units may be selected according to actual needs to achieve the purpose of the solution of this embodiment.

[0072] The above embodiments are only used to illustrate the technical solutions of the present application, rather than to limit them. Although the present application has been described in detail with reference to the aforementioned embodiments, those skilled in the art should understand that they can still modify the technical solutions described in the aforementioned embodiments, or make equivalent replacements for some of the technical features therein. These modifications or replacements do not deviate the essence of the corresponding technical solutions from the spirit and scope of the technical solutions of the embodiments of the present application, and should all be included in the protection scope of the present application.

Claims

1. A method for storing and sending biological samples for inspection, applied to a biological sample box, characterized in that: The method comprises: Acquire partition information of a target material box, wherein the partition information includes target material information of each partition of the target material box; Determine, based on the target sample information, an estimated inactivation time of the target sample and an estimated delivery time of the target sample to the first target delivery point; If the estimated delivery time exceeds the estimated inactivation time, obtaining the alternative delivery target point information of the target sample; According to the information of the candidate inspection target point, the candidate inspection target point closest to the target inspection material box is determined as the second target inspection point.

2. The method for storing and sending biological samples according to claim 1, characterized in that: The method further comprises: If the absolute value of the time difference between the estimated delivery time and the estimated inactivation time is less than a first preset threshold, obtaining a preset target sample sorting ratio; According to the target sample inspection ratio, a first portion of the target sample is sent to the first target inspection point, and a second portion of the target sample is sent to the second target inspection point.

3. The method for storing and sending biological samples according to claim 1, characterized in that: The method further comprises: Determining the estimated inactivation time of the target sample in each partition of the target sample box according to the partition information; According to the estimated inactivation time of the target samples in each partition, target samples whose estimated inactivation time is in the same preset estimated inactivation time period are determined as similar inactivation samples; If the ratio of the number of similar inactivated samples to the total number of samples in the target sample box reaches a preset ratio threshold, the target sample box is controlled to send a first prompt message to the target user.

4. The method for storing and sending biological samples for inspection according to claim 1, characterized in that: Before the step of obtaining the partition information of the target material inspection box, the method further includes: Obtain target sample input information entered by the target user; According to the input information of the target sample, determine whether there is a risk of sample contamination; If the sample contamination risk exists, a partition storage plan is generated according to the target sample corresponding to the sample contamination risk.

5. The method for storing and sending biological samples for inspection according to claim 4, characterized in that: The method further comprises: Determine the reason for sending the target sample for inspection according to the input information of the target sample; Determine the sample requirement information based on the reason for the sample submission; If the target sample information does not meet the sample requirement information, a second prompt message is sent to the target user.

6. The method for storing and sending biological samples for inspection according to claim 1, characterized in that: The method further comprises: According to the target sample information, obtaining matching parameter information of the target sample; According to the matching parameter information, the storage parameters of the partition where the target sample is located are adjusted to the matching parameters.

7. The method for storing and sending biological samples for inspection according to claim 6, characterized in that: The method further comprises: Acquire the storage parameter information of each partition of the target material box; A storage parameter report of the target sample box is generated according to the storage parameter information, and the storage parameter report is sent to the target user.

8. A biological sample storage and inspection system, characterized in that: include: A partition information acquisition module, used to acquire partition information of a target material box, wherein the partition information includes target material information of each partition of the target material box; A time estimation module, used to determine the estimated inactivation time of the target sample and the estimated delivery time of the target sample to the first target delivery point according to the target sample information; An alternative inspection point acquisition module is used to acquire the alternative inspection target point information of the target inspection material if the estimated delivery time exceeds the estimated inactivation time; The inspection point adjustment module is used to determine the alternative inspection target point closest to the target inspection material box as the second target inspection point according to the alternative inspection target point information.

9. An electronic device, characterized in that: The method comprises a memory and a processor, wherein the memory stores a computer program that can be loaded by the processor and executes the method for storing and sending biological samples for inspection as claimed in any one of claims 1 to 7.

10. A storage medium, characterized in that: A computer program is stored which can be loaded by a processor and execute the method for storing and submitting biological samples as claimed in any one of claims 1 to 7.

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