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
- 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
- Building and Installing gnuplot
- 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 CorrespondenceDNAscope LongRead pipelineStructural Variant Calling for PacBio HiFi and Oxford Nanopore long readsSomatic Variant Calling for SNPs and INDELsPCR Duplicate Removal With Consensus FunctionalityFunctional Equivalent Pipeline from CCDG using SentieonTNscope Somatic variant discovery with a matched normal sample using a machine learning modelUsing jemalloc to Optimize Memory AllocationBuilding and Installing gnuplotDescription of output files and fieldsRecommendations on Read GroupsDistributed ModeLicense Server ExtensionGermline Copy Number Variant Calling for Whole-Genome-Sequencing with CNVscopeDeployment Guide for Amazon Web ServicesDeployment Guide for Microsoft Azure