Haplotype aware diplotyping from noisy long reads

相關問題 & 資訊整理

Haplotype aware diplotyping from noisy long reads

Here, we introduce a novel statistical framework for the joint inference of haplotypes and genotypes from noisy long reads, which we term diplotyping. Our ... ,由 J Ebler 著作 · 2019 · 被引用 58 次 — Here, we introduce a novel statistical framework for the joint inference of haplotypes and genotypes from noisy long reads, which we term ... ,由 J Ebler 著作 · 2019 · 被引用 58 次 — The model ensures that each read stays in the same partition across variants, and hence does not “switch haplotypes,” something which is key to ... ,2018年4月12日 — Results In this paper we introduce a novel approach for haplotype-aware genotyping from noisy long reads. We do this by considering bipartitions ...

相關軟體 SlimBrowser 資訊

SlimBrowser
SlimBrowser 是一個完美的網絡瀏覽器,為電腦新手和專業人士,希望有一個瀏覽器的互聯網體驗,預裝了所有他們最喜歡的插件,附加組件和功能,否則他們可能會發現只有長期的測試無數的互聯網附加組件,為他們的瀏覽器。 SlimBrowser 通過提供每個包已經具有一些最受歡迎和最想要的功能,其他知名的瀏覽器,如 Internet Explorer,Chrome 和 Firefox 的基本包中不存在的... SlimBrowser 軟體介紹

Haplotype aware diplotyping from noisy long reads 相關參考資料
(PDF) Haplotype-aware diplotyping from noisy long reads

Here, we introduce a novel statistical framework for the joint inference of haplotypes and genotypes from noisy long reads, which we term diplotyping. Our ...

https://www.researchgate.net

Haplotype-aware diplotyping from noisy long reads

由 J Ebler 著作 · 2019 · 被引用 58 次 — Here, we introduce a novel statistical framework for the joint inference of haplotypes and genotypes from noisy long reads, which we term ...

https://genomebiology.biomedce

Haplotype-aware diplotyping from noisy long reads - PMC

由 J Ebler 著作 · 2019 · 被引用 58 次 — The model ensures that each read stays in the same partition across variants, and hence does not “switch haplotypes,” something which is key to ...

https://www.ncbi.nlm.nih.gov

Haplotype-aware genotyping from noisy long reads

2018年4月12日 — Results In this paper we introduce a novel approach for haplotype-aware genotyping from noisy long reads. We do this by considering bipartitions ...

https://www.biorxiv.org