טוען...
Common Copy Number Variation Detection From Multiple Sequenced Samples
Common copy number variations (CNVs) [1] are small regions of genomic variations at the same loci across multiple samples, which can be detected with high resolution from next-generation sequencing (NGS) technique. Multiple sequencing data samples are often available from genomic studies; examples i...
שמור ב:
| Main Authors: | , , |
|---|---|
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2014
|
| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4165854/ https://ncbi.nlm.nih.gov/pubmed/24557694 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1109/TBME.2013.2292588 |
| תגים: |
הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!
|