System and methods for high throughput screening of tissue preparation conditions
The present disclosure relates generally to systems and methods for screening sample preparation conditions and, more specifically, high throughput screening of tissue sample preparation conditions.
1 . A method, comprising:
affixing a microfluidic chip having a plurality of channels to a tissue sample such that a first channel of the plurality of channels traverses at least a first region of the tissue sample and a second channel of the plurality of channels traverses at least a second region of the tissue sample;
capturing a first image of the microfluidic chip affixed to the tissue sample that shows a position of at least the first channel and the second channel of the plurality of channels relative to the tissue sample;
flowing a plurality of reagents through the plurality of channels of the microfluidic chip, wherein flowing the plurality of reagents through the plurality of channels comprises:
flowing a first reagent through the first channel, wherein the first reagent interacts with the first region of the tissue sample; and
flowing a second reagent through the second channel, wherein the second reagent interacts with the second region of the tissue sample, wherein the first reagent differs from the second reagent and/or a first characteristic of the interaction between the first reagent and the first region differs from a second characteristic of the interaction between the second reagent and the second region;
removing the microfluidic chip from the tissue sample;
optically marking the tissue sample to identify a quality of the tissue sample and areas in the tissue sample affected by the flow of the plurality of reagents over the tissue sample;
capturing a second image of the tissue sample after removing the microfluidic chip;
co-registering the first and second images resulting in a separation of the second image into a plurality of image regions, wherein a first image region of the plurality of image regions is a first portion of the second image that includes the first region of the tissue sample and a second image region of the plurality of image regions is a second portion of the second image that includes the second region of the tissue sample; and
ranking a performance of the plurality of reagents with the tissue sample based on at least an average brightness of the optical markings captured in one or more image regions of the second image that correspond to a respective reagent of the plurality of reagents.
2 . The method of claim 1 , wherein the first reagent is a first concentration of a permeabilization agent and the second reagent is a second concentration of the permeabilization agent that is different than the first concentration.
3 . The method of claim 1 , wherein the first reagent is a first concentration of an active enzyme and the second reagent is a second concentration of the active enzyme that is different than the first concentration.
4 . The method of claim 1 , wherein the first characteristic differs from the second characteristic on account of the second reagent being flowed through the second channel a predetermined amount of time after the first reagent is flowed through the first channel such that a first incubation time for the first reagent is greater than a second incubation time for the second reagent.
5 . The method of claim 1 , wherein the microfluidic chip is a first microfluidic chip and the method further comprises:
affixing a second microfluidic chip to the tissue sample after removing the first microfluidic chip such that a plurality of channels of the second microfluidic chip are oriented in a different direction than the plurality of channels of the first microfluidic chip; and
flowing a second plurality of reagents through the plurality of channels of the second microfluidic chip.
6 . The method of claim 1 , wherein the ranking of the plurality of reagents is further based on a Pearson correlation between a brightness of a first type of optical marking and a brightness of a second type of optical marking.
7 . The method of claim 6 , wherein the first type of optical marking is generated by a fluorescent DNA stain that marks locations of the tissue sample containing double-stranded DNA.
8 . The method of claim 7 , wherein the second type of optical marking is generated by applying a linker oligo conjugated with a fluorescent molecule to the tissue sample, which marks locations of the tissue sample with transposition sites.
9 . The method of claim 8 , wherein the ranking of the plurality of reagents is further based on a probability transposition sites and double-stranded DNA locations overlap each other.
10 . The method of claim 7 , wherein the second type of optical marking is generated by a fluorescent antibody, which marks locations of the tissue sample that contain a particular type of protein.
11 . The method of claim 10 , wherein the particular type of protein is a glial fibrillary acidic protein.
12 . The method of claim 1 , wherein the first reagent includes a first antibody having a first concentration and the second reagent includes the first antibody having a second concentration different than the first concentration.
13 . The method of claim 12 , wherein optically marking the tissue sample comprises applying a second antibody to the tissue sample, wherein the second antibody is configured to bind with the first antibody and emit a fluorescent light.
14 . The method of claim 1 , wherein co-registering the first and second images further comprises grouping the plurality of image regions into groups corresponding to each of the plurality of reagents.
15 . A non-transitory computer-readable storage medium storing one or more programs, the one or more programs comprising instructions, which when executed by one or more processors of an electronic system, cause the electronic system to:
affix a microfluidic chip having a plurality of channels to a tissue sample such that a first channel of the plurality of channels traverses at least a first region of the tissue sample and a second channel of the plurality of channels traverses at least a second region of the tissue sample;
capture a first image of the microfluidic chip affixed to the tissue sample that shows a position of at least the first channel and the second channel of the plurality of channels relative to the tissue sample;
flow a plurality of reagents through the plurality of channels of the microfluidic chip, wherein flowing the plurality of reagents through the plurality of channels comprises:
flowing a first reagent through the first channel, wherein the first reagent interacts with the first region of the tissue sample; and
flowing a second reagent through the second channel, wherein the second reagent interacts with the second region of the tissue sample, wherein the first reagent differs from the second reagent and/or a first characteristic of the interaction between the first reagent and the first region differs from a second characteristic of the interaction between the second reagent and the second region;
removing the microfluidic chip from the tissue sample;
optically mark the tissue sample to identify a quality of the tissue sample and areas in the tissue sample affected by the flow of the plurality of reagents over the tissue sample;
capture a second image of the tissue sample after removing the microfluidic chip;
co-register the first and second images resulting in a separation of the second image into a plurality of image regions, wherein a first image region of the plurality of image regions is a first portion of the second image that includes the first region of the tissue sample and a second image region of the plurality of image regions is a second portion of the second image that includes the second region of the tissue sample; and
rank a performance of the plurality of reagents with the tissue sample based on at least an average brightness of the optical markings captured in one or more image regions of the second image that correspond to a respective reagent of the plurality of reagents.
16 . A non-transitory computer-readable storage medium storing one or more programs, the one or more programs comprising instructions, which when executed by one or more processors of an electronic system, cause the electronic system to:
receive a first image of a microfluidic chip having a plurality of channels that was affixed to a tissue sample such that a first channel of the plurality of channels traverses at least a first region of the tissue sample and a second channel of the plurality of channels traverses at least a second region of the tissue sample;
receive a second image of the tissue sample after:
a plurality of reagents were flowed through the plurality of channels of the microfluidic chip, wherein flowing the plurality of reagents through the plurality of channels comprised:
flowing a first reagent through the first channel, wherein the first reagent interacts with the first region of the tissue sample; and
flowing a second reagent through the second channel, wherein the second reagent interacts with the second region of the tissue sample, wherein the first reagent differs from the second reagent and/or a first characteristic of the interaction between the first reagent and the first region differs from a second characteristic of the interaction between the second reagent and the second region;
removing the microfluidic chip from the tissue sample; and
optically marking the tissue sample to identify a quality of the tissue sample and areas in the tissue sample affected by the flow of the plurality of reagents over the tissue sample;
co-register the first and second images resulting in a separation of the second image into a plurality of image regions, wherein a first image region of the plurality of image regions is a first portion of the second image that includes the first region of the tissue sample and a second image region of the plurality of image regions is a second portion of the second image that includes the second region of the tissue sample; and
rank a performance of the plurality of reagents with the tissue sample based on at least an average brightness of the optical markings captured in one or more image regions of the second image that correspond to a respective reagent of the plurality of reagents.