Automated processing and annotation of NGS data
Professional software that does not require special skills to use
Automated processing and annotation of NGS data
Professional software that does not require special skills to use
NGS Wizard is not tied to a certain sequencer and will process data from various platforms: Illumina, Oxford Nanopore, Ion Torrent, SeqLL, BGI. Recognition of the platform and data types will be automatics.
The program is available through a web browser. Data is stored in Germany datacenter in accordance with the strict European data protection regulations. It is possible to store data on internal servers of an organization so the data doesn’t leave its perimeter.
Thanks to NGS Wizard, one can reduce the time for technical data processing several times. The program offers a wide range of tools for professional bioinformatics with the ability to step-by-step track the entire analysis process and perform analysis according to its own pipeline.
Based on special AI algorithms developed by Novel. The program can be used by people without special knowledge in the technical analysis of genomic data - doctors, scientists, bio-engineers and even common people.
The reports show clinically significant variants for a given nosology and incidental findings for other nosologies; targeted drugs of categories A, B, as well as C, D, E; mutation rates from internal database and errors of serial effects; Recommended clarifications of the diagnosis based on the pattern of mutations; mutational load (for tumors) and more.
Allows to find mutations and genomic polymorphisms and annotate them using connected databases for scientific research.
Users are BioTech companies, academic organizations, experimental medicine organizations, universities.
Allows to find mutations and provide statistical estimates of the development of diseases. Users are Academics, experimental medicine organizations, prenatal genetic testing clinics, as well as insurance companies and individual consumers.
Interprets all mutations in the tumor and/or blood, helps doctors to clarify the diagnosis and prescribe targeted therapy for cancer patients, as well as optimize the course of treatment. The module will be expanded . Users are oncology clinics, experimental medicine organizations.
Allows to identify aneuploidies and other chromosomal rearrangements in samples when sequencing whole-genome DNA with low coverage. Users are clinics providing prenatal / preimplantation diagnostics and IVF services.
Determines the composition of bacteria and viruses in a sample of saliva, soil, food, and provides information of their pathogenicity. Users are- monitoring organizations and BioTech companies.
Provides qualitative statistical assessments of the development of diseases and predicts the physiological properties of the genome’s owner. D2C users are- the segment for individual consumers. B2B users are insurance companies and public health systems.
Displays a list of drugs that are contraindicated for a carrier of genomic polymorphism data. Users are individual consumers, pharmacies, public health systems.
A new module of the Genomenal platform for assessing polygenic risks of common diseases will be developed in cooperat
The British edition of Data Magazine, owned by the London media company Fupping LTD, based on information from Crunch
A new version of NGS Wizard 1.5.1 was released. The following additional features have emerged in this product:
FAQ
User-friendly interface, modern tools, detailed data processing pipelines. Different reports can be created for various nosologies, unlike universal programs. The program starts automatically and all the processing stages pass independently before getting the result; there is no need to start and control every step.
The program is available in the cloud and does not require installation, you just need to create an account. It can be deployed to client servers, then the process can take several hours.
No additional qualifications are required to work with the NGS Wizard.The program can be used by anyone - a doctor, a student, a specialist with no experience in medical genetics.
You can now process data from Illumina and BGI/MGI equipment. The program is not tied to a specific platform and will further process data from other sequencers.
It is possible to upload readings directly from the sequencer in FASTQ format, mapping in SAM/BAM format or genetic variants in VCF format without any additional processing.
Now it is possible to configure and customize existing pipelines directly to NGS WIzard, but we are ready to create any pipeline according to your order as an exclusive or public module.
At the moment, pipelines for processing somatic and germinal point variants (SNV), indels, copy number changes (CNV) and structural genome variations (SV) are supported, however, we are ready to offer the development of any pipeline in a short time.
The number of simultaneously processed samples is limited only by the existing computing power, and the customized automatic bioinformatics processing process can be applied to any batch of samples in automatic mode.
Yes, a fully functional trial version of NGS Wizard is provided free of charge and we will be glad to take into account your wishes in the development of the platform. Upon request, we will conduct a detailed presentation of the platform and answer all the questions.
Processing of genomic data using the NGS Wizard is possible both online (in cloud) and on the client’s server. We offer flexible options for different tasks.
Cloud platform for automated processing and annotation of NGS data. Prices on demand