Lv1
48 积分 2024-11-08 加入
A robust benchmark for detection of germline large deletions and insertions
15天前
已完结
Structural variant calling using Sniffles2
27天前
已完结
Clinical Long-Read Genome Sequencing for Rare-Disease Diagnostics
1个月前
已完结
Haplotype-aware variant calling with PEPPER-Margin-DeepVariant enables high accuracy in nanopore long-reads
1个月前
已完结
Deep learning: new computational modelling techniques for genomics
2个月前
已完结
Haplotype-aware variant calling with PEPPER-Margin-DeepVariant enables high accuracy in nanopore long-reads
2个月前
已完结
Structural variation in the sequencing era
2个月前
已完结
A robust benchmark for detection of germline large deletions and insertions
2个月前
已完结
Severus detects somatic structural variation and complex rearrangements in cancer genomes using long-read sequencing
3个月前
已完结
A synthetic-diploid benchmark for accurate variant-calling evaluation
3个月前
已完结
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