लोड हो रहा है...
Phasing for medical sequencing using rare variants and large haplotype reference panels
Motivation: There is growing recognition that estimating haplotypes from high coverage sequencing of single samples in clinical settings is an important problem. At the same time very large datasets consisting of tens and hundreds of thousands of high-coverage sequenced samples will soon be availabl...
में बचाया:
| में प्रकाशित: | Bioinformatics |
|---|---|
| मुख्य लेखकों: | , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Oxford University Press
2016
|
| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4920110/ https://ncbi.nlm.nih.gov/pubmed/27153703 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btw065 |
| टैग : |
टैग जोड़ें
कोई टैग नहीं, इस रिकॉर्ड को टैग करने वाले पहले व्यक्ति बनें!
|