Bioinformatics: Secondary Celemics Analysis Service: Variant calls & annotations and visualized mutation analysis report

Description

Secondary Celemics Analysis Service

• Upload Your FASTQ files and receive annotated Variant Call Format (VCF) files for the called variants
plus comprehensive visualized reports about CNV, Indels, Fusions, TMB, MSI etc.
• Please contact us to let us know your project details and to receive a quotation

Although NGS-based molecular analysis technologies have advanced rapidly, existing bioinformatics analysis platforms have not matched the speed of development.
Even as the discovery of various new biomarkers and their applications are becoming more
prevalent day by day, there are very few solutions in the market that are able to readily
react to client needs.
As such, Celemics have developed the Celemics Analysis Service (CAS), a revolutionary
bioinformatics solution aiming to provide client-specific services based on the expertise of its bioinformatics analysts.

The Secondary Celemics Analysis Service includes the following steps:

• Filtration of the Raw FASTQ Data (Adapter-Removal) and FASTQ QC
• Alignment and Sorting of Sequences
• Removal of PCR Duplicates
• Base Quality Recalibration
• Mapping Quality Filtration
• Annotation and provision of annotated VCF files
• Variant Filtration: Mutation Detection using metrics such as VAF, depth, and strand conditions
• Provision of visualized report about CNV, Indels, Fusions, TMB, MSI etc.

Tertiary analysis including the variant analysis in terms of clinical relevance is also offered by Celemics.

Please contact us to let us know your project details and to receive a quotation