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Mikhail Kolmogorov

University of California San Diego
H指数:25
被引数:1.4万

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Long-read sequencing of single cell-derived melanoma sublines reveals divergent and parallel genomic and epigenomic evolutionary trajectories

单细胞衍生的黑色素瘤亚系的长期测序揭示了不同的平行基因组及表观基因组进化轨迹

2026-07-160
OAAI
Haplotype-resolved genome assemblies of BJ and IMR-90 human fibroblast cell lines reveal extensive structural variation and enable reanalysis of historical sequencing data

BJ和IMR-90人成纤维细胞系的单倍型解析基因组组装揭示广泛的基因组结构变异,并能够重新分析历史测序数据

2026-04-290
OA
Proof-of-concept study for the detection of somatic structural variant driver alterations using HiFi long-read sequencing in a pediatric leukemia cohort

使用高保真长读长测序检测儿科白血病队列中体细胞结构变异驱动突变的可行性研究

2026-04-090
OA
Accurate somatic small variant discovery for multiple sequencing technologies with DeepSomatic

使用deepsmatoma实现多种测序技术的准确体细胞小变异发现

2025-10-160
PRE
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
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
Severus detects somatic structural variation and complex rearrangements in cancer genomes using long-read sequencing

Severus通过长读长测序检测癌症基因组中的体细胞结构变异和复杂重排

2025-04-041
PRE
Advancing long-read nanopore genome assembly and accurate variant calling for rare disease detection

推进长读纳米孔基因组组装和精确变异呼吁罕见疾病检测

2025-02-011
PRE
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
Personalized pangenome references
2024-09-111
PRE
A polymorphic TERT tandem repeat creating an expandable intronic G4 quadruplex is associated with TERT expression, relative leukocyte telomere length and cancer risk

产生可扩展内含子G4四链体的多态性TERT串联重复序列与TERT表达,相对白细胞端粒长度和癌症风险相关

2024-03-220
PRE
Insights into the mechanisms and structure of breakage-fusion-bridge cycles in cervical cancer using long-read sequencing
2024-03-011
OAAI