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 Germline variant calling with a machine learning model
- DNAscope for HiFi reads
- 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 Azure
- Download AppNote PDFs:
Arguments CorrespondenceDNAscope Germline variant calling with a machine learning modelDNAscope for HiFi readsStructural Variant Calling for PacBio HiFi and Oxford Nanopore long readsSomatic Variant Calling for SNPs and INDELsUnique Molecular IdentifiersPCR 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 AllocationDescription of output files and fieldsRecommendations on Read GroupsDistributed ModeLicense Server ExtensionCopy Number VariantDeployment Guide for Amazon Web ServicesDeployment Guide for Microsoft Azure