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A Robust Approach for Blind Detection of Balanced Chromosomal Rearrangements with Whole-Genome Low-Coverage Sequencing
2小时前
待确认
CNV_IFTV: An Isolation Forest and Total Variation-Based Detection of CNVs from Short-Read Sequencing Data
22小时前
已完结
High resolution global chromosomal aberrations from spontaneous miscarriages revealed by low coverage whole genome sequencing
1天前
已完结
Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing
1天前
已完结
Copy Number and SNP Arrays in Clinical Diagnostics
1天前
已完结
Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing
1天前
已完结
胎儿染色体非整倍体21三体、18三体和13三体检测试剂盒(高通量测序法)行业标准的制定
2个月前
已完结
The origin and evolution of the pseudoautosomal regions of human sex chromosomes
3个月前
已完结
Variant calling and benchmarking in an era of complete human genome sequences
3个月前
已完结
病原宏基因组高通量测序 技术质量控制与评价的挑战和思考
4个月前
已完结
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