ERD

Functional Analysis of Structural Variants in Single Cells using Strand-seq

Project: MOSAIC

Updated at: 13-08-2024

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Project acronym MOSAIC

Recurrent inversion polymorphisms in humans associate with genetic instability and genomic disorders

Project: MOSAIC

Updated at: 13-08-2024

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Project acronym MOSAIC

Single-cell strand sequencing of a macaque genome reveals multiple nested inversions and breakpoint reuse during primate...

Project: MOSAIC

Updated at: 27-04-2024

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Project acronym MOSAIC

Haplotype-resolved diverse human genomes and integrated analysis of structural variation

Project: MOSAIC

Updated at: 27-04-2024

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Project acronym MOSAIC

VISOR: a versatile haplotype-aware structural variant simulator for short- and long-read sequencing

Project: MOSAIC

Updated at: 27-04-2024

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Project acronym MOSAIC

Cell type-specific consequences of mosaic structural variants in hematopoietic stem and progenitor cells

Project: MOSAIC

Updated at: 27-04-2024

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Project acronym MOSAIC

Haplotype-Aware Single-Cell Multiomics Uncovers Functional Effects of Somatic Structural Variation

Project: MOSAIC

Updated at: 27-04-2024

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Project acronym MOSAIC

MosaiCatcher v2: a single-cell structural variations detection and analysis reference framework based on Strand-seq

Project: MOSAIC

Updated at: 27-04-2024

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Project acronym MOSAIC

Periodic Reporting for period 3 - MOSAIC (Relationship of Somatic Structural Variation Mosaicism to Aging and Disease Ph...

Project: MOSAIC

Updated at: 27-04-2024

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Project acronym MOSAIC

Single-cell analysis of structural variations and complex rearrangements with tri-channel processing

Project: MOSAIC

Updated at: 27-04-2024

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Project acronym MOSAIC

COMPREHENSIVE DETECTION OF SINGLE CELL GENETIC STRUCTURAL VARIATIONS

Project: MOSAIC

Updated at: 27-04-2024

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Project acronym MOSAIC

Recurrent inversion toggling and great ape genome evolution

Project: MOSAIC

Updated at: 27-04-2024

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Project acronym MOSAIC

COMPREHENSIVE DETECTION OF SINGLE CELL GENETIC STRUCTURAL VARIATIONS

Project: MOSAIC

Updated at: 27-04-2024

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Project acronym MOSAIC

Fully phased human genome assembly without parental data using single-cell strand sequencing and long reads

Project: MOSAIC

Updated at: 27-04-2024

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Project acronym MOSAIC

Multi-platform discovery of haplotype-resolved structural variation in human genomes

Project: MOSAIC

Updated at: 27-04-2024

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Project acronym MOSAIC

Haplotype-resolved inversion landscape reveals hotspots of mutational recurrence associated with genomic disorders

Project: MOSAIC

Updated at: 27-04-2024

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Project acronym MOSAIC

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Functional Analysis of Structural Variants in Single Cells using Strand-seq

Recurrent inversion polymorphisms in humans associate with genetic instability and genomic disorders

Single-cell strand sequencing of a macaque genome reveals multiple nested inversions and breakpoint reuse during primate...

Haplotype-resolved diverse human genomes and integrated analysis of structural variation

VISOR: a versatile haplotype-aware structural variant simulator for short- and long-read sequencing

Cell type-specific consequences of mosaic structural variants in hematopoietic stem and progenitor cells

Haplotype-Aware Single-Cell Multiomics Uncovers Functional Effects of Somatic Structural Variation

MosaiCatcher v2: a single-cell structural variations detection and analysis reference framework based on Strand-seq

Periodic Reporting for period 3 - MOSAIC (Relationship of Somatic Structural Variation Mosaicism to Aging and Disease Ph...

Single-cell analysis of structural variations and complex rearrangements with tri-channel processing

COMPREHENSIVE DETECTION OF SINGLE CELL GENETIC STRUCTURAL VARIATIONS

Recurrent inversion toggling and great ape genome evolution

COMPREHENSIVE DETECTION OF SINGLE CELL GENETIC STRUCTURAL VARIATIONS

Fully phased human genome assembly without parental data using single-cell strand sequencing and long reads

Multi-platform discovery of haplotype-resolved structural variation in human genomes

Haplotype-resolved inversion landscape reveals hotspots of mutational recurrence associated with genomic disorders