Lv661
1800 积分 2021-08-05 加入
Unveiling novel genetic variants in 370 challenging medically relevant genes using the long read sequencing data of 41 samples from 19 global populations
6天前
已完结
Rapid Detection of Hemoglobinopathy Variants Using One-Step Library Preparation and Nanopore Sequencing
1个月前
已完结
Rapid Detection of Hemoglobinopathy Variants Using One-Step Library Preparation and Nanopore Sequencing
1个月前
已完结
Enhancing siRNA efficacy in vivo with extended nucleic acid backbones
1个月前
已完结
From bench to bedside: Improving the clinical safety of GalNAc-siRNA conjugates using seed-pairing destabilization
1个月前
已完结
Fragile X Syndrome Carrier Screening Using a Nanopore Sequencing Assay
1个月前
已完结
Evaluating the clinical utility of a long-read sequencing-based approach in genetic testing of fragile-X syndrome
2个月前
已完结
SNP calling, haplotype phasing and allele-specific analysis with long RNA-seq reads
4个月前
已完结
Comprehensive Assays for Incontinentia Pigmenti Using Long-Read Sequencing and its Application in Preimplantation Genetic Testing
5个月前
已完结
An Effective and Universal Long-Read Sequencing-Based Approach for SMN1 2 + 0 Carrier Screening through Family Trio Analysis
6个月前
已完结
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