Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications.
High-throughput DNA sequencing technology has transformed genetic research and is starting to make an impact on clinical practice. However, analyzing high-throughput sequencing data remains challenging, particularly in clinical settings where accuracy and turnaround times are critical. We present a...
| Հիմնական հեղինակներ: | , , , , , , , |
|---|---|
| Ձևաչափ: | Journal article |
| Լեզու: | English |
| Հրապարակվել է: |
Nature Publishing Group
2014
|
Search Result 1
Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications
Հրապարակվել է 2014
Journal article