Business Description and Basis of Presentation [Text Block] | 1. Veracyte, Inc., or Veracyte, or the Company, is a global genomic diagnostics company that improves patient care by providing answers to clinical questions to inform diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The Company’s growing menu of genomic tests leverage advances in genomic science and technology to change care for patients, enabling them to avoid risky, costly procedures and quicken time to appropriate treatment. With Veracyte’s exclusive global access to a best-in-class diagnostics instrument platform, the Company is positioned to deliver its tests to patients worldwide through laboratories and hospitals that can perform the tests locally. Veracyte was incorporated in the state of Delaware on August 15, 2006 2008. March 4, 2008, one The Company offers genomic tests in four Thyroid Cancer - Afirma Genomic Sequencing Classifier and Xpression Atlas. The Afirma Xpression Atlas complements the Afirma GSC by providing genomic alteration content from the same FNA samples used in Afirma GSC testing to help physicians decide with greater confidence on the surgical or therapeutic pathway for their patients. The Company commercially launched the Afirma Xpression Atlas in 2018 April 2020 Lung Cancer - Percepta Genomic Sequencing Classifier. second June 2019. may may IPF - Envisia Genomic Classifier. Breast Cancer - Prosigna Breast Cancer Prognostic Gene Signature Assay. December 2019 50 PAM50 ten The Company performs its genomic tests for thyroid cancer, lung cancer and IPF in its CLIA-certified laboratory in South San Francisco, California. In December 2019, The Company’s approach also provides multiple opportunities for partnerships with biopharmaceutical and diagnostic testing companies. In developing its products, the Company has built or gained access to unique biorepositories, proprietary technology and bioinformatics that it believes are important to the development of new targeted therapies, determining clinical trial eligibility and guiding treatment selection. Additionally, the Company believes that the nCounter system, with its ability to simultaneously analyze RNA, DNA or protein targets in up to 800 Basis of Presentation The Company’s condensed consolidated financial statements have been prepared in accordance with accounting principles generally accepted in the United States, or GAAP. Certain information and note disclosures normally included in financial statements prepared in accordance with GAAP have been condensed or omitted pursuant to such rules and regulations. The condensed consolidated balance sheet as of September 30, 2020 three nine September 30, 2020 2019 three nine September 30, 2020 2019 nine September 30, 2020 2019 December 31, 2019 three nine September 30, 2020 not The accompanying interim period condensed consolidated financial statements and related financial information included in this Quarterly Report on Form 10 10 December 31, 2019 Reclassifications Certain prior period balances have been reclassified to conform to current period presentation of the Company’s condensed consolidated financial statements and accompanying notes. Such reclassifications have no September 30, 2019 Use of Estimates The preparation of unaudited interim financial statements in conformity with GAAP requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent liabilities as of the date of the financial statements and the reported amounts of revenue and expenses during the reporting period. Items subject to such estimates include: revenue recognition; write-down of supplies; the useful lives of property and equipment; the recoverability of long-lived assets; the incremental borrowing rate for leases; the estimation of the fair value of intangible assets and contingent consideration; variable interest entity assessment; impairment of equity investment, at cost; stock options; income tax uncertainties, including a valuation allowance for deferred tax assets; reserve on accounts receivable and contingencies. The Company bases these estimates on historical and anticipated results, trends, and various other assumptions that the Company believes are reasonable under the circumstances, including assumptions as to future events. These estimates form the basis for making judgments about the carrying values of assets and liabilities and recorded revenue and expenses that are not Issuance of Common Stock in a Public Offering On August 7, 2020, On May 7, 2019, Cash and Cash Equivalents The Company considers demand deposits in a bank, money market funds and highly liquid investments with an original maturity of 90 three third September 30, 2020 Equity Investment In July 2020, $1.0 not not not not 321, September 30, 2020 September 30, 2020. Concentrations of Credit Risk and Other Risks and Uncertainties The worldwide spread of coronavirus, or COVID- 19, no 19 may 19 19 may 19 The majority of the Company’s cash and cash equivalents are deposited with one may not Several of the components of the Company’s sample collection kits and test reagents, and the nCounter system and related diagnostic kits are obtained from single-source suppliers. If these single-source suppliers fail to satisfy the Company’s requirements on a timely basis, it could suffer delays in being able to deliver its diagnostic solutions, a possible loss of revenue, or incur higher costs, any of which could adversely affect its operating results. The Company is also subject to credit risk from its accounts receivable related to its sales. Credit risk for accounts receivable from testing revenue is incorporated in testing revenue accrual rates as the Company assesses historical collection rates and current developments to determine accrual rates and amounts the Company will ultimately collect. The Company generally does not not not September 30, 2020 Through September 30, 2020 third 10% Three Months Ended September 30, Nine Months Ended September 30, 2020 2019 2020 2019 Medicare 25 % 26 % 24 % 24 % Johnson and Johnson Services, Inc. * 13 % * 12 % UnitedHealthcare 11 % 11 % 11 % 11 % 36 % 50 % 35 % 47 % *Less than 10% The Company’s third 10% September 30, 2020 December 31, 2019 Johnson and Johnson Services, Inc. * 10 % Medicare 12 % 15 % UnitedHealthcare 10 % * *Less than 10% Restricted Cash The Company had deposits of $603,000 included in long-term assets as of September 30, 2020 December 31, 2019 Revenue Recognition Testing Revenue The Company recognizes testing revenue in accordance with the provisions of ASC 606, 606. During 2020, three nine September 30, 2020 zero three nine September 30, 2020 During 2019, three nine September 30, 2019 zero three nine September 30, 2019 Product Revenue The Company began recognizing product revenue in December 2019, 4 Product revenue from instruments and diagnostic kits is recognized generally upon shipment or when the instrument is ready for use by the end customer, which is when title of the product has been transferred to the customer. This process involves identifying the contract with a customer, determining the performance obligations in the contract, determining the contract price, allocating the contract price to the distinct performance obligations in the contract, and recognizing revenue when the performance obligations have been satisfied. A performance obligation is considered distinct from other obligations in a contract when it provides a benefit to the customer either on its own or together with other resources that are readily available to the customer and is separately identified in the contract. Performance obligations are considered satisfied once the Company has transferred control of a product to the customer, meaning the customer has the ability to use and obtain the benefit of the product. The Company recognizes product revenue for satisfied performance obligations only when there are no Biopharmaceutical and Collaboration Revenue From time to time, the Company enters into arrangements for research and development and/or laboratory services. Such arrangements may In arrangements involving more than one The consideration allocated to each distinct performance obligation is recognized as revenue when control of the related goods is transferred or services are performed. Consideration associated with at-risk substantive performance milestones is recognized as revenue when it is probable that a significant reversal of the cumulative revenue recognized will not Collaborative Arrangements The Company enters into collaborative arrangements with partners that fall under the scope of ASC Topic 808, 808. 808, may 606 606 The terms of the Company’s collaborative arrangements typically include one may Net sales of data or other services to our customers are classified under biopharmaceutical revenue, and all other non-customer revenue are classified under collaboration revenue in our consolidated statements of operations and comprehensive loss. There was no collaboration revenue in the three nine September 30, 2020 As part of the accounting for these arrangements, the Company must develop estimates and assumptions that require judgment to determine the underlying stand-alone selling price for each performance obligation which determines how the transaction price is allocated among the performance obligations. Generally, the estimation of the stand-alone selling price may Up-front Fees: If a license to the Company’s intellectual property is determined to be distinct from the other performance obligations identified in the arrangement, the Company recognizes revenues from the transaction price allocated to the license when the license is transferred to the licensee and the licensee is able to use and benefit from the license. For licenses that are bundled with other promises, the Company utilizes judgment to assess the nature of the combined performance obligation to determine whether the combined performance obligation is satisfied over time or at a point in time. Milestone Payments: At the inception of each arrangement that includes milestone payments (variable consideration), the Company evaluates whether the milestones are considered probable of being reached and estimates the amount to be included in the transaction price using the most likely amount method. If it is probable that a significant revenue reversal would not not not may Services Agreement with Loxo Oncology On April 9, 2018, one one may September 30, 2020 not 606 nine September 30, 2019 nine September 30, 2020 three nine September 30, 2020 not September 30, 2020 December 31, 2019 Diagnostic Development Agreement with Johnson & Johnson On December 28, 2018, v.2, two v.2 not Under the terms of the agreement, the Company will provide data from its RNA whole-transcriptome sequencing platform to JJSI in exchange for $7.0 million in payments from JJSI. The Company is also entitled to additional payments from JJSI of up to $13.0 million, conditioned upon the achievement of certain milestones relating to the development and reimbursement of the Percepta v.2 ten first v.2 one v.2 December 18, 2019, nine September 30, 2020 The JJSI agreement is considered to be within the scope of ASC 808, 606 606, $7.0 $13.0 not The Company recognized revenue of $0.3 million and $1.5 million for three nine September 30, 2020 three nine September 30, 2019 v.2 v.2 three nine September 30, 2019 September 30, 2020 December 31, 2019 September 30, 2020 December 31, 2019 Collaboration Agreement with AstraZeneca Group On December 23, 2019, three nine September 30, 2020 zero September 30, 2020 Commercial Development Agreement with CareDx On May 13, 2020, three nine September 30, 2020 zero September 30, 2020 Cost of Testing Revenue The components of our cost of testing services are laboratory expenses, sample collection expenses, compensation expense, license fees and royalties, depreciation and amortization, other expenses such as equipment and laboratory supplies, and allocations of facility and information technology expenses. Costs associated with performing tests are expensed as the test is processed regardless of whether and when revenue is recognized with respect to that test. Cost of testing revenue for the nine September 30, 2020 19 Cost of Product Revenue Cost of product revenue consists primarily of costs of purchasing instruments and diagnostic kits from third Cost of Biopharmaceutical Revenue Cost of biopharmaceutical revenue consists of costs of performing activities under arrangements that require the Company to perform research and development services on behalf of a customer pursuant to a biopharmaceutical service agreement. Recent Accounting Pronouncements In June 2016, No. 2016 13, Financial Instruments-Credit Losses: Measurement of Credit Losses on Financial Instruments January 1, 2020. not In November 2018, No. 2018 18, Collaborative Arrangements (Topic 808 606 not 606. December 15, 2019, 2019 no In August 2018 No. 2018 15, Intangibles—Goodwill and Other—Internal-Use Software (Subtopic 350 40 January 1, 2020 no In August 2018, No. 2018 13, Fair Value Measurement (Topic 820 2018 13. 2018 13 1 1 2 2 3 3 1 3 2 3 may 3 2018 13 January 1, 2020 2018 13 not 3 5, |