Upon sign-up, the organisation administrator will select one of the following options: There are different types of HIV drug-resistance assays that organisations can use to perform drug-resistance testing on Sanger DNA sequencing machines. What do you need to know about my organisation? Organisational accounts offer benefits over individual accounts, particularly for quality assurance purposes. The administrator will also set each user's account privileges, as either an administrator or not. These users will be prompted to accept an invitation to the organisation from the administrator after sign-up, when they first log in. Once your organisation is approved, the first registered user for an organisation will be designated as the вЂњAdministratorвЂќ - this administrator will be able to add further users as members of that organisation by inviting them via email. Each user is grouped into a new or existing organisation if you are the first person from your organisation to to sign up to Exatype Sanger HIV, you will be asked to provide information about your organisation when you first login. You can sign up to Exatype Sanger HIV by creating an account at. Organisations, laboratories and individuals carrying out HIV drug-resistance testing can sign up to use Exatype. Who should sign up for Exatype Sanger HIV? The sequence data for each sample are then analysed individually and sample-specific HIV drug-resistance reports are produced. Sequence data (.ab1 files) are uploaded either manually (by a user) or automatically (directly from the sequencing machine) to the Exatype website. What is Exatype Sanger HIV?Д®xatype Sanger HIV is an end-to-end computational workflow for HIV drug-resistance analysis and reporting.

ab1 format from Sanger sequencing machines) directly from a DNA sequencing machine, and Exatype will analyse it and produce a simple, clear report for each sample that was sequenced. Upload your raw data (either in fastq/fastq.gz format from next-generation sequencing machines, or. The Exatype service is an accurate method of detecting mutations in sequencing data.

Sanger sequencing chromatogram viewer