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J

Jean Monlong

university of california
H指数:34
被引数:1.8万

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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
Personalized pangenome references
2024-09-111
PRE
Phased nanopore assembly with Shasta and modular graph phasing with GFAse

用Shasta进行的分相纳米孔组装和用GFAse进行的模块化图形分相

2024-04-163
OA
Evolution of chromosome-arm aberrations in breast cancer through genetic network rewiring
2024-04-016
OAAI
Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation
2023-09-1428
OA
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
Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition (vol 52, pg 306, 2020)

全基因组的泛癌症分析确定了由LINE-1反转录转座促进的驱动程序重排 (第52卷,306页,2020页)

2023-03-211
OAAI
Glioblastoma scRNA-seq shows treatment-induced, immune-dependent increase in mesenchymal cancer cells and structural variants in distal neural stem cells
2022-04-1317
OA
Ultra-Rapid Nanopore Whole Genome Genetic Diagnosis of Dilated Cardiomyopathy in an Adolescent With Cardiogenic Shock
2022-04-012
OA
Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencing
2022-03-2848
OAAI
Ultrarapid Nanopore Genome Sequencing in a Critical Care Setting

重症监护环境中的超微粒纳米孔基因组测序

2022-02-17111
OA
Invasive growth associated with cold-inducible RNA-binding protein expression drives recurrence of surgically resected brain metastases
2021-01-1222
OAAI
Pangenomics enables genotyping of known structural variants in 5202 diverse genomes
Science
IF45.8
2021-01-010
OAAI
Single-cell RNA-seq reveals that glioblastoma recapitulates a normal neurodevelopmental hierarchy (vol 11, 3406, 2020)
2020-08-073
OAAI
Single-cell RNA-seq reveals that glioblastoma recapitulates a normal neurodevelopmental hierarchy
2020-07-08312
OAAI
Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes

纳米孔测序和Shasta工具包可以有效地从头组装11个人类基因组

2020-05-04282
OAAI