Quick Start - Retrieval

const axios = require('axios');

const YOUR_DOPPLERAI_API_KEY = 'sk-...' // Replace with your API Key
const headers = { Authorization: `Bearer ${YOUR_DOPPLERAI_API_KEY}` };

// Create chat
async function createChat(headers, chatData) {
    const chatsUrl = 'https://api.dopplerai.com/v1/chats';
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        return response.data;
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        console.log(error);
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}

// The reference_id and name are optional.
// If you don't need them, pass in an empty object: chatData = {}
const chatData = {
    "reference_id": "ac52d6a60a3b489683fd6cfda6e4abcd",
    "name": "User A"
};

createChat(headers, chatData)
    .then(response => console.log(response));
// { reference_id: 'ac52d6a60a3b489683fd6cfda6e4abcd', name: 'User A', uuid: 'ad289875-c446-4799-a017-14cda80d18c1', created_at: '2023-06-24T22:24:00.447256' }

const axios = require('axios');

const YOUR_DOPPLERAI_API_KEY = 'sk-...' // Replace with your API Key
const headers = { 'Authorization': `Bearer ${YOUR_DOPPLERAI_API_KEY}` };

// Create collection
async function createCollection(headers, collectionData) {
    const collectionsUrl = 'https://api.dopplerai.com/v1/collections';
    try {
        const response = await axios.post(collectionsUrl, collectionData, { headers: headers });
        return response.data;
    } catch (error) {
        console.log(error);
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}

const collectionData = {
    "reference_id": "fb700444788d430bb39b148447af7521",
    "name": "reports"
};

createCollection(headers, collectionData)
    .then(response => {
        console.log(response);
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// {'name': 'reports', 'reference_id': 'fb700444788d430bb39b148447af7521', 'uuid': 'e3aa752c-ede3-4c45-8088-67f0671bfc19', 'created_at': '2023-06-25T00:51:31.526000'}

const axios = require('axios');

const YOUR_DOPPLERAI_API_KEY = 'sk-...'; // Replace with your API Key
const headers = { 'Authorization': `Bearer ${YOUR_DOPPLERAI_API_KEY}` };

// Upload URL
async function uploadUrl(headers, uploadData) {
    const uploadsUrl = 'https://api.dopplerai.com/v1/uploads/url';
    try {
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        return response.data;
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        console.log(error);
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}

const uploadData = {
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};

uploadUrl(headers, uploadData)
    .then(response => {
        console.log(response);
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// { name: 'Acute Bronchitis', reference_id: null, uuid: '0d11c591-3dc7-495b-af72-0189b80147b4', created_at: '2023-06-25T20:27:38.532505', collection_uuid: 'e3aa752c-ede3-4c45-8088-67f0671bfc19', content: 'Warning: The NCBI web site requires JavaScript to function. more... ...', info: 'Added upload to vector database' }

const axios = require('axios');

const YOUR_DOPPLERAI_API_KEY = 'sk-...'; // Replace with your API Key
const headers = { 'Authorization': `Bearer ${YOUR_DOPPLERAI_API_KEY}` };

// Upload Text
async function uploadText(headers, uploadData) {
    const uploadsUrl = 'https://api.dopplerai.com/v1/uploads/text';
    try {
        const response = await axios.post(uploadsUrl, uploadData, { headers: headers });
        return response.data;
    } catch (error) {
        console.log(error);
    }
}

const content = `
Introduction
Acoustic neuroma is also called vestibular schwannoma (VS), acoustic neurinoma, vestibular neuroma or acoustic neurofibroma. These are tumors that evolve from the Schwann cell sheath and can be either intracranial or extra-axial. They usually occur adjacent to the cochlear and vestibular nerves and most often arise from the inferior division of the latter. Anatomically, acoustic neuroma tends to occupy the cerebellopontine angle. About 5-10% of cerebellopontine angle (CPA) tumors are meningiomas and may occur elsewhere in the brain. Bilateral acoustic neuromas tend to be exclusively found in individuals with type 2 neurofibromatosis.[1][2][3]

Etiology
Bilateral acoustic neuromas may be a part of neurofibromatosis type 2 occurring due to a defect on chromosome 22q12.2 at the location of the neurofibromin 2 gene which encodes merlin protein. Studies have shown that acoustic neuroma had a causative predisposition mutation. Radiation exposure may predispose a patient to the development of that condition as well.[4] Even though mobile phone radiation has been of concern, several studies have failed to prove its causative effect on vestibular schwannomas.[5]

Epidemiology
Approximately 8% of all intracranial tumors which manifest clinically are attributed to schwannomas. The majority of acoustic neuromas are unilateral and sporadic. Bilateral acoustic neuromas are in fact genetic and constitute a bit less than 5% of all schwannomas. Acoustic neuromas in general, tend to present between the fourth to sixth decades of life. Acoustic neuromas developing in individuals with neurofibromatosis type 2 (NF II) are likely to present earlier, with a peak incidence around the third decade of life. Although rare, acoustic schwannomas can occur in children. There is a small female preponderance with an aggravation of problems during pregnancy. The hereditary acoustic neuroma occurs in NF II much more often compared to neurofibromatosis type 1 (NF I), although the latter is much more common. Unilateral acoustic neuroma has been reported exclusively in 24% of cases with NF I, while bilateral acoustic schwannoma is a hallmark of NF II. Both these conditions are autosomal dominant. The defective genetic locus has been localized to chromosome 17 in NF I and chromosome 22 in NF II.[6][7]
`;

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};

uploadText(headers, uploadData)
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        console.log(response);
    });
// {'name': 'Acoustic Neuroma', 'uuid': '1d8fd24f-26f6-4e77-a7fd-84465cef55be', 'created_at': '2023-06-25T02:27:47.877907', 'collection_uuid': 'e3aa752c-ede3-4c45-8088-67f0671bfc19', 'content': 'Introduction ...', 'info': 'Added upload to vector database'}

const axios = require('axios');

const YOUR_DOPPLERAI_API_KEY = 'sk-...'; // Replace with your API Key
const headers = { 'Authorization': `Bearer ${YOUR_DOPPLERAI_API_KEY}` };

// Send Message
async function sendMessage(headers, messageData) {
    const messagesUrl = 'https://api.dopplerai.com/v1/messages';
    try {
        const response = await axios.post(messagesUrl, messageData, { headers: headers });
        return response.data;
    } catch (error) {
        console.log(error);
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}

const chatUuid = "ad289875-c446-4799-a017-14cda80d18c1";

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sendMessage(headers, messageData)
    .then(response => {
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        console.log(response.completion.choices[0].message.content);
        // Acoustic neuromas may be a part of neurofibromatosis type 2 occurring due to a defect on chromosome 22q12.2 at the location of the neurofibromin 2 gene which encodes merlin protein. The hereditary acoustic neuroma occurs in NF II much more often compared to neurofibromatosis type 1 (NF I), although the latter is much more common. Unilateral acoustic neuroma has been reported exclusively in 24% of cases with NF I, while bilateral acoustic schwannoma is a hallmark of NF II. Both these conditions are autosomal dominant.
    });