Welcome to Sentieon® Application Notes

Below is a list of application notes for Sentieon® Genomics Software Suite. If you have any questions regarding the content below, please contact the technical support at Sentieon® Inc. at support@sentieon.com.

• Arguments Correspondence
• DNAscope LongRead
• Structural variant calling for PacBio HiFi and Oxford Nanopore long reads
• Somatic Variant Calling for SNPs and Indels
• Unique Molecular Identifiers
• PCR Duplicate Removal With Consensus Functionality
• Functional Equivalent Pipeline from CCDG using Sentieon®
• TNscope® Somatic variant discovery with a matched normal sample using a machine learning model
• Using jemalloc to Optimize Memory Allocation
• Description of output files and fields
• Recommendations on Read Groups
• Distributed Mode
• License Server Extension
• Germline Copy Number Variant Calling for Whole-Genome-Sequencing with CNVscope
• Deployment Guide for Amazon Web Services
• Deployment Guide for Azure

Download AppNote PDFs:

• Arguments Correspondence

• DNAscope LongRead pipeline

• Structural Variant Calling for PacBio HiFi and Oxford Nanopore long reads

• Somatic Variant Calling for SNPs and INDELs

• Unique Molecular Identifiers

• PCR Duplicate Removal With Consensus Functionality

• Functional Equivalent Pipeline from CCDG using Sentieon

• TNscope Somatic variant discovery with a matched normal sample using a machine learning model

• Using jemalloc to Optimize Memory Allocation

• Description of output files and fields

• Recommendations on Read Groups

• Distributed Mode

• License Server Extension

• Copy Number Variant

• Deployment Guide for Amazon Web Services

• Deployment Guide for Microsoft Azure