low coverage whole genome sequencing

Genotyping by low-coverage whole-genome sequencing in intercross pedigrees from outbred founders: a cost-efficient appr...

low coverage whole genome sequencing

Genotyping by low-coverage whole-genome sequencing in intercross pedigrees from outbred founders: a cost-efficient approach. Yanjun Zan , ..., Low coverage whole genome sequencing (lcWGS; for example, 0.5X coverage) followed by imputation is a potential alternative approach to ...

相關軟體 Miranda 資訊

Miranda
Miranda 即時通訊是一個小型,快速,易於使用的即時通訊軟件,它支持多種協議和許多用戶界面和服務功能,可以使所有知識水平的用戶輕鬆地在一個應用程序內統一所有的朋友,帳戶和聊天會話。它速度非常快,使用的系統資源非常少,不需要安裝,甚至可以安裝在單個軟盤或 USB 驅動器上,並且無需安裝在 PC 上即可運行。默認情況下,Miranda IM 只帶有一些基本功能,但其功能總是通過添加(現在超過 35... Miranda 軟體介紹

low coverage whole genome sequencing 相關參考資料
Extremely low-coverage sequencing and imputation increases ...

Here, we show that extremely low-coverage sequencing (0.1-0.5×) captures ... Low coverage whole genome sequencing enables accurate assessment of ...

https://europepmc.org

Genotyping by low-coverage whole-genome sequencing in ...

Genotyping by low-coverage whole-genome sequencing in intercross pedigrees from outbred founders: a cost-efficient approach. Yanjun Zan , ...

https://gsejournal.biomedcentr

Low coverage whole genome sequencing enables ... - bioRxiv

Low coverage whole genome sequencing (lcWGS; for example, 0.5X coverage) followed by imputation is a potential alternative approach to ...

https://www.biorxiv.org

Low coverage whole genome sequencing enables ... - PubMed

Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores.

https://pubmed.ncbi.nlm.nih.go

Low coverage whole genome sequencing enables accurate ...

Low coverage whole genome sequencing (lcWGS; for example, 0.5× coverage) followed by imputation is a potential alternative to genotyping ...

https://genomemedicine.biomedc

Low-Coverage Whole Genome Sequencing - National Cancer ...

https://www.cancer.gov

Phylogenomics from Low-coverage Whole-genome Sequencing

Phylogenomics from low- coverage whole- genome sequencing. Feng Zhang1,2,3 | Yinhuan Ding1 | Chao-Dong Zhu2,4 | Xin Zhou5 |. Michael C. Orr2 ...

https://www.researchgate.net

Whole Genome Low-Coverage Sequencing ... - Frontiers

Whole Genome Low-Coverage Sequencing Concurrently Detecting Copy Number Variations and Their Underlying Complex Chromosomal ...

https://www.frontiersin.org