Lv51
1170 积分 2023-03-07 加入
[Introduction and interpretation of the updated contents of the International System for Human Cytogenomic Nomenclature]
1小时前
已完结
A multivariate modeling method for the prediction of low fetal fraction before noninvasive prenatal testing
1个月前
已完结
Determination of fetal DNA fraction from the plasma of pregnant women using sequence read counts
1个月前
已完结
Creating basis for introducing non‐invasive prenatal testing in the Estonian public health setting
1个月前
已完结
A Local Outlier Factor-Based Detection of Copy Number Variations From NGS Data
4个月前
已完结
CNV_IFTV: An Isolation Forest and Total Variation-Based Detection of CNVs from Short-Read Sequencing Data
4个月前
已完结
Haplotype-aware variant calling with PEPPER-Margin-DeepVariant enables high accuracy in nanopore long-reads
1年前
已完结
Assembly of 43 diverse human Y chromosomes reveals extensive complexity and variation
1年前
已完结
Long-read mapping to repetitive reference sequences using Winnowmap2
1年前
已完结
Linear: a framework to enable existing software to resolve structural variants in long reads with flexible and efficient alignment-free statistical models
1年前
已完结
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