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The present invention provides devices and systems for use at the point of care. The methods devices of the invention are directed toward automatic detection of analytes in a bodily fluid. The components of the device are modular to allow for flexibility and robustness of use with the disclosed meth

The present invention provides devices and systems for use at the point of care. The methods devices of the invention are directed toward automatic detection of analytes in a bodily fluid. The components of the device are modular to allow for flexibility and robustness of use with the disclosed methods for a variety of medical applications.

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1. A device for detection of an analyte in a bodily fluid sample comprising: a sample collection unit configured to receive the bodily fluid sample;an array of assay units configured to receive a portion of the sample from the sample collection unit and configured to run a chemical reaction that yie

1. A device for detection of an analyte in a bodily fluid sample comprising: a sample collection unit configured to receive the bodily fluid sample;an array of assay units configured to receive a portion of the sample from the sample collection unit and configured to run a chemical reaction that yields a detectable signal indicative of the presence of the analyte in the sample; andan array of reagent units configured to contain reagents for running the chemical reaction; wherein an individual assay unit comprises an assay tip that is configured to receive the portion of the sample and the reagents, when the assay unit is moved into fluid communication with the reagent unit,wherein the assay tip comprises a first opening on the first side of the tip and a second opening on a second side of the tip, wherein the first opening has a diameter greater than that of the second opening, andwherein the assay tip comprises an interior surface having immobilized thereon reagents for detecting said analyte. 2. The device of claim 1, wherein the sample collection unit is configured to receive a volume of the bodily fluid sample of about 20 microliters or less. 3. The device of claim 1, wherein the sample collection unit is configured to receive a volume of the bodily fluid sample that is a single drop of blood. 4. The device of claim 1 further comprising a pretreatment unit configured to retrieve a portion of the bodily fluid sample for running the chemical reaction to detect the analyte. 5. The device of claim 4, wherein the bodily fluid is a whole blood sample and the portion is plasma. 6. The device of claim 4, wherein the sample collection unit is configured to receive a sample tip that collects at least a portion of the bodily fluid sample. 7. The device of claim 6, wherein the pretreatment unit or the individual assay unit is configured to receive the sample tip, which distributes the bodily fluid sample to said pretreatment unit or individual assay unit. 8. The device of claim 7, wherein the pretreatment unit is configured to receive a pretreatment tip that collects the sample from the pretreatment unit. 9. The device of claim 8, wherein the individual assay unit is configured to receive the sample tip or the pretreatment tip, which distributes the bodily fluid sample to the individual assay unit. 10. The device of claim 1, wherein the individual assay unit is movable from one location of the device to another. 11. The device of claim 10, wherein the individual reagent unit is configured to receive the movable assay unit in said device. 12. The device of claim 11, wherein the individual reagent unit is configured to receive within its cavity at least a portion of the movable assay tip in said device. 13. The device of claim 11 wherein the assay tip is configured to be moved from a first reagent unit to a second reagent unit. 14. The device of claim 11 wherein the second opening of the assay tip is configured to permit reagents to be distributed to the assay tip according to an aspiration- or pipette-type action provided to the assay tip. 15. The device of claim 1, wherein the individual assay unit comprises immunoassay reagents for running an immunoassay. 16. The device of claim 1, wherein the bodily fluid sample is a blood sample. 17. The device of claim 1, wherein the assay units and the reagent units are addressable to indicate the location of the units on the device. 18. The device of claim 17, wherein the individual reagent unit of the array is addressed to correspond to an individual assay unit in the device. 19. The device of claim 18, wherein the individual reagent unit and the individual assay unit are aligned in a column or in a row in the device. 20. The device of claim 1 further comprising a housing configured to receive the array of assay units and the array of reagent units. 21. A system for detection of an analyte in a bodily fluid sample comprising: a. a device of claim 1; andb. a detection assembly for detecting the detectable signal indicative of the presence or absence of the analyte. 22. The system of claim 21 further comprising a programmable mechanical device configured to move the individual assay unit from a first location to a second location. 23. The system of claim 21 further comprising a fluid transfer device. 24. The system of claim 23, wherein the fluid transfer device is a pipette. 25. The system of claim 24 wherein the pipette is an air-displacement pipette. 26. The system of claim 23, wherein the fluid transfer device is automated. 27. The system of claim 23, wherein the fluid transfer device comprises a plurality of heads, wherein an individual head of the plurality of heads is configured to engage the individual assay unit. 28. The system of claim 23, wherein the fluid transfer device comprises a programmable processor configured to direct fluid transfer of the bodily fluid sample from the sample collection unit and a reagent from an individual reagent unit to the individual assay unit. 29. The system of claim 28, wherein the configuration of the processor to direct fluid transfer effects a degree of dilution of the bodily fluid sample in the array of assay units to bring signals indicative of the analyte being detected within a detectable range, such that said analyte is detectable with said system. 30. The system of claim 21 further comprising a communication assembly for transmitting a protocol based on the analyte to be detected. 31. The system of claim 21 further comprising a heating block configured to receive the individual assay unit. 32. The system of claim 21, wherein the sample collection unit is operably linked to a magnetic block to effect regeneration of plasma from the bodily fluid, wherein the bodily fluid is a blood sample. 33. The device of claim 1, wherein the assay tip comprises an opening at one end from which sample or reagent is transferred in and out of the assay tip. 34. The device of claim 1, wherein the second opening of the assay tip is configured to permit a wash solution to enter and drain therethrough. 35. The device of claim 34, wherein the second opening of the assay tip is configured to permit the aspiration of wash solution into the assay tip. 36. A method of using automated immunoassay for detecting an analyte present in plasma portion of a whole blood sample, comprising: a. providing a whole blood sample to the device of claim 1;b. detecting a signal; andc. transmitting result of (b) to an end user. 37. The method of claim 36, wherein the immunoassay is ELISA. 38. The method of claim 36, wherein the result is transmitted wirelessly.