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Nathan D. Olson

national institute of standards and technology
H指数:38
被引数:1.2万

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Characterization of subclonal variants in HG002 Genome in a Bottle reference material as a resource for benchmarking variant callers

HG002基因组参考材料中子克隆变异体的表征,作为评估变异检测算法的资源

2026-04-010
OAAI
Correction: Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pair

更正:开发和广泛测序一个得到广泛认可的“Genome in a Bottle”匹配的肿瘤-正常配对样本

2025-08-080
OAAI
The Platinum Pedigree: a long-read benchmark for genetic variants

铂金血统:一种用于遗传变异的长读基准

2025-08-040
OA
Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pair

开发并广泛测序一种在Genome in a Bottle框架下获得广泛共识的匹配肿瘤-正常样本对

2025-07-160
OAAI
Small variant benchmark from a complete assembly of X and Y chromosomes

X和Y染色体完整组装的小变异基准测试

2025-01-080
OA
High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation

对来自1000基因组项目的样品进行高覆盖纳米孔测序,以建立人类遗传变异的综合目录

2024-10-027
PRE
Pangenome graph construction from genome alignments with Minigraph-Cactus

用minigrap-cactus从基因组比对构建Pangenome图

2023-05-1049
OA
A draft human pangenome reference

人类pangenome参考草案

Nature
IF48.5
2023-05-100
OAAI
PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regions

PrecisionFDA真相挑战V2: 在难以映射的区域中从短读和长读调用变体

2022-05-0157
OAAI
Benchmarking challenging small variants with linked and long reads

具有链接和长读取的具有挑战性的小变体的基准测试

2022-05-0151
OAAI
Curated variation benchmarks for challenging medically relevant autosomal genes

具有挑战性的医学相关常染色体基因的策划变异基准

2022-02-0776
OAAI
The complete sequence of a human genome

人类基因组的完整序列

Science
IF45.8
2022-01-010
OAAI
Zero-Valent Iron Sand Filtration Can Reduce Human and Plant Pathogenic Bacteria While Increasing Plant Growth Promoting Bacteria in Reclaimed Water
2020-11-029
OAAI