18 Nov 2025
Accelerated and High-Accuracy Variant Calling on ONT Sequencing Data with the Sentieon DNAscope LongRead and Hybrid Pipelines
doi.org/10.1101/2025.11.14.6…
Comparison of read mapping and variant calling tools for the analysis of plant NGS data
doi.org/10.1101/2020.03.10.9…
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17 Nov 2025
Accelerated and High-Accuracy Variant Calling on Oxford Nanopore Technologies Sequencing Data with the Sentieon DNAscope LongRead ... biorxiv.org/content/10.1101/… #biorxiv_bioinfo
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16 Jul 2025
＼🎁新規購入で14万円相当が無償🎁／
RNAscope™シリーズご購入キャンペーン🎉🎉
RNAscope™ / BaseScope™ / miRNAscope™ / DNAscope™
すべて対象です🧐🔍
RNA単一分子をin situで検出＆定量できる独自のハイブリ技術🔬FFPE組織、凍結組織、培養細胞もOK👌✨
🔗cosmobio.co.jp/product/detai…
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1,393
2 Jul 2025
＼ご注目👀✨／
RNAscope™ / BaseScope™ / miRNAscope™ / DNAscope™
コスモ・バイオからまだご購入いただいたことのない方へ
試薬キット＋ターゲットプローブ ご購入で
ターゲットプローブ1点を【無償提供】🎊
📅キャンペーンは9月30日まで
この機会にぜひお試しを🥰
🔗cosmobio.co.jp/new/campaign/…
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21 Apr 2025
DNAscope Hybrid accepts Fasta or BAM files as input and generates VCF outputs containing SNP, indel, SV, and CNV data. DNAscope Hybrid can be used with whole-genome sequencing long-read data or with targeted sequencing approaches like the Twist Alliance Dark Genes Panel.
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21 Apr 2025
The DNAscope Hybrid pipeline significantly improves SNP and Indel calling accuracy, particularly in complex genomic regions. At lower long-read depths, the hybrid approach outperforms standalone short- or long-read pipelines at full sequencing depths.
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21 Apr 2025
DNAscope Hybrid accepts Fasta or BAM files as input and generates VCF outputs containing SNP, indel, SV, and CNV data. DNAscope Hybrid can be used with whole-genome sequencing long-read data or with targeted sequencing approaches like the Twist Alliance Dark Genes Panel.
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21 Apr 2025
The DNAscope Hybrid pipeline significantly improves SNP and Indel calling accuracy, particularly in complex genomic regions. At lower long-read depths, the hybrid approach outperforms standalone short- or long-read pipelines at full sequencing depths.
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21 Apr 2025
DNAscope Hybrid: Accelerated, Accurate, Hybrid Short and Long Reads Alignment and Variant Calling biorxiv.org/content/10.1101/…
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24 Jul 2023
Pretty pictures of DNAscope technique showing HIV DNA detected in brain myeloid cells, and other recent work has shown that this is replication competent.
Much work to understand how CNS reservoirs work and are regulated, but imagine the leaps in progress when we do!
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Their work will – for the first time - enable systematic interrogation of spatial distribution patterns and microenvironmental interactions of tumor subclones in-situ in the same tissue section, combining state of the art #MIBIscope, #DNAscope and scRNA-seq.
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1 May 2023
Happy brighter Monday! Delighted to share #RNAscope has more than 7K pubs; below is link to few of 2022 pubs covering variety of apps incl. #spatialgeneexpression, #ASO/#siRNA, #celltherapy n #DNAscope to detect amplification in EVs biotechne.egnyte.com/fl/0vJe…
#singlecell #scRNA
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29 Mar 2023
aws.amazon.com/blogs/hpc/cos…
Currently at ~$1.70 on-demand ~$0.80 spot, well under an hour. Can run BWA/gatk best practices or more accurate pipeline DNAscope
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19 Jan 2023
“@sentieon’s DNAscope pipeline for @ElemBio finished in 35 minutes with an On-Demand compute cost of $1.69.”
30x human WGS on #AVITI !
I'm a big fan of @sentieon's applications for analyzing genomics data.
Read this post about cost-effective and accurate genomics analysis with Sentieon on AWS
aws.amazon.com/blogs/hpc/cos… via @awscloud
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18 Jan 2023
Excerpt: In this blog post, we benchmark the performance of Sentieon’s DNAseq and DNAscope pipelines using publicly available genomics datasets on AWS. You will gain an understanding of the runtime, cost, and accuracy performance of these germline variant calling [1/2]
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13 Jan 2023
“Further analysis by DNAscope showed a low-level of detectable HIV DNA in 33% of the liver samples. In liver tissue, HIV DNA was detected in CD4 T-cells and hepatocytes” infectiousdiseaseadvisor.com…
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16 Nov 2022
We are proud to have supported @sentieon's germline variant-calling pipeline DNAscope achieved superior SNP and indel accuracy as compared to other standard datasets, based on MGI’s DNBSEQ-G400 sequencing platform. Read more here: en.mgi-tech.com/news/356/
genomeweb.com/sequencing/mgi…
15 Nov 2022
MGI Sequencing Platform and Sentieon Machine Learning Model Enable Improved Small Variant Calling Accuracy for Whole-Genome Sequencing Data. DNAscope, a germline variant-calling pipeline from San Jose-based analytics firm Sentieon, achieved superior... ow.ly/63ME104ejhn
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