variant calls – The Sequencing Center

How to create Geneious variant call reports

Geneious Reports We have numerous clients who use Geneious for bioinformatics data analysis. They use Geneious for sequence alignments of their sample datasets against reference genomes and for the interpretation of Geneious variant call…

Whole Genome Sequencing bioinformatics, Geneious, genome sequence alignment, variant calls

Geneious sequence alignment & variant calls workflow

Geneious Prime is one of many bioinformatics tools that our clients use to post-process sequencing datasets. Geneious includes an extensive set of functions to perform sequence alignments of sample reads against reference genomes. And it…

Whole Genome Sequencing bioinformatics, Geneious, variant calls, whole genome sequencing

How to read Geneious variant call reports

Reading Geneious Reports Our clients often use Geneious to generate SNP/indel variant call reports. A truncated report is available here. (The number of SNP's/indels in a typical report can be quite large so we only show a few records…

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The Sequencing Center is one of the leading service providers for HLA Typing and Whole Genome Sequencing (WGS) in the USA. Offering affordable, high-coverage HLA typing results with 4-field resolution and microbial scale WGS, we provide clients with exceptional services, including DNA extraction, library prep, sequencing and bioinformatics. We work with leading research organizations world-wide in various fields including immunology, oncology, transplantation, inherited diseases, neurodegenerative diseases, and drug discovery and development.

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