Calling All Variants: Award Winning Software For Short & Long Read Sequencing

Presented by

Don Freed, PhD, Sr. Bioinformatics Scientist & Brendan Gallagher, Head of Business Development, Sentieon

About this talk

Learn state of the art variant calling to make the most of your genomic data with award winning, highly accurate and cost-effective Secondary Analysis Software for bioinformatics data processing from Sentieon. Process Fastq>(G)VCF data processing on your own VPC or in Amazon Omics. The Sentieon software produces SNP, INDEL, and Structural Variation using any NGS platform. • Learn how easy it is to process Pacbio Revio, Illumina, MGI/BGI, Element Biosciences, Ultima Genomics, and Oxford Nanopore Technologies Data into high quality SNV, INDEL, and Structural Variants • Learn cost and performance metrics for these pipelines on Amazon Omics and in AWS EC2 • Learn about additional data processing applications including somatic variant calling, and processing of RNAseq, UMI, and single-cell data. ____________________________ Sentieon® develops award winning, extremely accurate and highly-optimized algorithms and software for bioinformatics data processing applications. Sentieon® is a team of engineers with deep expertise in algorithm, software, and system optimization. Using our accumulated expertise in modeling, optimization, machine learning, and high-performance computing, we strive to enable precision data for precision medicine.
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