
London Calling 2023 is now live
Register for your free virtual conference ticket to hear the very latest research from scientists using nanopore sequencing in their work
99%以上のリード単位精度を取得するQ20+ケミストリ
V14とR10.4.1ポアを組み合わせたキットにより最高の精度を実現 • デュプレックス法によりQ30以上の精度を実現 • 収量、速度、マルチプレックスなどの点で最適なソリューションLondon Calling 2023: Technology update
Hear about breakthrough technology performance and our pathway to enabling sequencing by anyone, anywhere.Genomics England long-read cancer whole-genome sequencing pilot
Helen Webb discussed the impact of identifying the correct variants in a fast, scalable, and cost-efficient manner, and how we can translate this research into clinical settings.- “This was almost a year of clinical testing, and it took about 24 hours to figure this out in our lab”Danny Miller(米国のワシントン大学)
- “…structural variant calls were highly accurate and complete, showing improvement over the current short-read and long-read methods”Mikhail Kolmogorov et al., NIH
Uncover the environmental microbial world
Unlocking the microbiome of the International Space Station, detecting previously undetected parasitising elements & borg extrachromosomal genomes were all discussed at London Calling 2023.Data analysis tools: methylation & phasing
Hear how the four researchers shared the latest tools being developed for the analysis of DNA methylation genome-wide and for methylation-based haplotype phasing at London Calling 2023- “We can detect SNPs with an F1 score better than [short reads]…& can discover structural variants with an F1 score comparable to state-of-the-art methods...but obviously with a lower cost.”Kimberley Billingsley, NIH Center for Alzheimer's and Related Dementias
99%以上のリード単位精度を取得するQ20+ケミストリ
V14とR10.4.1ポアを組み合わせたキットにより最高の精度を実現 • デュプレックス法によりQ30以上の精度を実現 • 収量、速度、マルチプレックスなどの点で最適なソリューションLondon Calling 2023: Technology update
Hear about breakthrough technology performance and our pathway to enabling sequencing by anyone, anywhere.Genomics England long-read cancer whole-genome sequencing pilot
Helen Webb discussed the impact of identifying the correct variants in a fast, scalable, and cost-efficient manner, and how we can translate this research into clinical settings.- “This was almost a year of clinical testing, and it took about 24 hours to figure this out in our lab”Danny Miller(米国のワシントン大学)
- “…structural variant calls were highly accurate and complete, showing improvement over the current short-read and long-read methods”Mikhail Kolmogorov et al., NIH
Uncover the environmental microbial world
Unlocking the microbiome of the International Space Station, detecting previously undetected parasitising elements & borg extrachromosomal genomes were all discussed at London Calling 2023.Data analysis tools: methylation & phasing
Hear how the four researchers shared the latest tools being developed for the analysis of DNA methylation genome-wide and for methylation-based haplotype phasing at London Calling 2023- “We can detect SNPs with an F1 score better than [short reads]…& can discover structural variants with an F1 score comparable to state-of-the-art methods...but obviously with a lower cost.”Kimberley Billingsley, NIH Center for Alzheimer's and Related Dementias
99%以上のリード単位精度を取得するQ20+ケミストリ
V14とR10.4.1ポアを組み合わせたキットにより最高の精度を実現 • デュプレックス法によりQ30以上の精度を実現 • 収量、速度、マルチプレックスなどの点で最適なソリューションLondon Calling 2023: Technology update
Hear about breakthrough technology performance and our pathway to enabling sequencing by anyone, anywhere.Genomics England long-read cancer whole-genome sequencing pilot
Helen Webb discussed the impact of identifying the correct variants in a fast, scalable, and cost-efficient manner, and how we can translate this research into clinical settings.- “This was almost a year of clinical testing, and it took about 24 hours to figure this out in our lab”Danny Miller(米国のワシントン大学)
- “…structural variant calls were highly accurate and complete, showing improvement over the current short-read and long-read methods”Mikhail Kolmogorov et al., NIH
Uncover the environmental microbial world
Unlocking the microbiome of the International Space Station, detecting previously undetected parasitising elements & borg extrachromosomal genomes were all discussed at London Calling 2023.Data analysis tools: methylation & phasing
Hear how the four researchers shared the latest tools being developed for the analysis of DNA methylation genome-wide and for methylation-based haplotype phasing at London Calling 2023- “We can detect SNPs with an F1 score better than [short reads]…& can discover structural variants with an F1 score comparable to state-of-the-art methods...but obviously with a lower cost.”Kimberley Billingsley, NIH Center for Alzheimer's and Related Dementias
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ナノポアシークエンスは研究者に以下を提供できる唯一の技術です。
ショートリードからウルトラロングリードまで、どんな長さのDNA/RNA断片でもシークエンス可能
ニーズに合わせてシークエンス収量を調整可能(最大14 Tb)
解析データをリアルタイムで取得
簡易かつ迅速なワークフローまたは自動ワークフロー
最新試薬やキットごとに装置を新しく買いなおす必要はありません
詳細な生物学的解析
SNP & INDEL
メチル化
構造変異
フェージング
アセンブリ
技術の用途
当社のプラットフォームは、ヒト、植物、動物、病原菌、環境に関わる生物学的疑問の探究に用いられることで、実社会の課題を解決しています。また、医療や食物の安全性などの「応用」領域での活用も増えています。
詳細