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Optical genome mapping for complex and cryptic chromosomal rearrangements detection in unsolved adverse pregnancy couples

Mendeley Data2026-04-09 收录

染色体结构变异

不良妊娠遗传病因分析

数据链接：

https://data.mendeley.com/datasets/n5hrjpfsbx/1 数据链接链接失效反馈

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资源简介：

OGM BNX summaries of case2

案例2的OGM BNX摘要

应用场景：

染色体结构变异

基因组学分析

Centromeric and telomeric motif and genotype distribution in the study population.

Figshare2018-04-18 更新40

Chromosome-scale scaffolding of de novo genome assemblies based on chromatin interactions. Homo sapiens

元基因组组装

染色体结构变异

HiC chromatin conformation sequencing was performed for the purpose of chromosome fusion and structural rearrangement identification.

NIAID Data Ecosystem30

Breakpoint re-use in S. cerevisiae.

染色体结构变异

基因组重排分析

aRatio of expected to observed breakpoints.bFive inversion events occur at telomeres, so each makes only one breakpoint.c21 breakpoints are shared by a reciprocal translocation and an inversion.

Figshare2015-12-02 更新20

GGT-linked genes present in human LCR22s*.

基因组注释

染色体结构变异

GGT-linked genes present in human LCR22s*.

Figshare2020-03-26 更新40

GigaMUGA SNP data of wild mice from Barcelona Robertsonian System (BRbS). GigaMUGA SNP data of wild mice from Barcelona Robertsonian System (BRbS)

种群遗传学

染色体结构变异

The Barcelona Robertsonian system (BRbS) presents mice with standard karyotype (diploid number 40) but also carrying Robertsonian fusions (ehich lead to variable diploid numbers ranging from 28 to 39)

NIAID Data Ecosystem20

Optical genome mapping for complex and cryptic chromosomal rearrangements detection in unsolved adverse pregnancy couples

资源简介：

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