SNF-CLIMEDIN: A Randomized Trial of Digital Support and Intervention in Patients With Advanced Non–Small Cell Lung Cancer. A Hellenic Cooperative Oncology Group Study Shallow whole-genome sequencing ...
Purpose: The purpose of this research was to assess the effectiveness of copy number variation sequencing (CNV-Seq) and quantitative fluorescence polymerase chain reaction (QF-PCR) in detecting ...
The art of finding patterns or communities plays a central role in the analysis of structured data such as networks. Community detection in graphs has become a field on its own. Real-world networks, ...
I've used Savana to detect both CNVs and SVs in a tumor-normal pair with 40x coverage (ONT). But when looking at the SV vcf, I find no matching deletion/duplication as the CNV algorithm. For SV, it ...
Abstract: Copy number variation (CNV) is a remarkable manifestation of genomic structural variations that affect human health. However, CNV detection in low coverage and low purity data is one of the ...
State Key Laboratory of Electronic Thin Films and Integrated Devices, School of Optoelectronic Science and Engineering, University of Electronic Science and Technology of China (UESTC), Chengdu 610054 ...
Reported Data Supports the Potential Extension of HD-MAP Vaccine Delivery to Oncology Indications Recently published data generated by researchers at The University of Queensland and Vaxxas shows ...
Abstract: Read depth (RD) signals anomaly-based copy number variation (CNV) detection methods using whole genome sequencing data are affected by the measurement scale and parameters, and the ...
A variety of new technologies aim to improve wildfire detection and help map the spread of blazes Anna Fiorentino - Freelance writer Embers from the Eaton Fire fly down a residential street in ...