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Sentieon Genomics 2025.03 Linux

Sentieon Genomics software is a set of software tools that perform analysis of genomic data obtained from DNA sequencing.The Sentieon® Genomics software enables rapid and accurate analysis of next-generation sequence data. The Sentieon® DNAseq pipelines enable germline variant calling on hundreds of thousands of samples simultaneously. The Sentieon® TNseq pipelines enable accurate calling of somatic variants in paired tumor-normal samples or in an unpaired tumor samples. The Sentieon® Genomics software produces more accurate results than other tools on third-party benchmarks with results obtained in one tenth the time of comparable pipelines.

Release 202503

Type Description
Feature Added support for hybrid short and long-read variant calling.
Feature Added support for reading and writing CRAM version 3.1 files.
Feature Added support in GVCFtyper algorithm for joint calling DNAscope GVCFs from long reads pipeline.
Feature Added support in TNscope algorithm to output FADF1R2, and F2R1 annotations.
Feature Added option in GCBias and AlignmentStat algorithms to match with Picard IS_BISULFITE_SEQUENCED option.
Feature Reduced memory utilization in HsMetricAlgo algorithm.
Bug-fix Solved issue in driver where minor inconsistencies in alignment @SQ records can cause an error.
Bug-fix Solved issue in consensus Dedup where paired consensus reads may not have matching read names.
Bug-fix Solved issue in LongReadSV algorithm that could cause a crash under rare circumstances.
Bug-fix Solved issue in DNAscope and Haplotyper that could cause an assertion when using the –bam_output option.
Bug-fix Solved issue in consensus Dedup that would cause the job to hang when –metrics is turned on.
Bug-fix Solved issue in TNhaplotyper2 in given mode that may produce incorrect results.
Bug-fix Solved issue in TNscope that missed low-AF variants at the site of germline homozygous variants.
Other Removed umi consensus from the software package.
Other Removed gnuplot binary from the software package.

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