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使用高密度寡核苷酸阵列快速检测患有多种先天性异常儿童的亚微观染色体重排。

Rapid detection of submicroscopic chromosomal rearrangements in children with multiple congenital anomalies using high density oligonucleotide arrays.

作者信息

Ming Jeffrey E, Geiger Elizabeth, James Alison C, Ciprero Karen L, Nimmakayalu Manjunath, Zhang Yi, Huang Andrew, Vaddi Madhavi, Rappaport Eric, Zackai Elaine H, Shaikh Tamim H

机构信息

Division of Human Genetics, Stokes Research Institute, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.

出版信息

Hum Mutat. 2006 May;27(5):467-73. doi: 10.1002/humu.20322.

Abstract

Chromosomal rearrangements such as microdeletions and interstitial duplications are the underlying cause of many human genetic disorders. These disorders can manifest in the form of multiple congenital anomalies (MCA), which are a significant cause of morbidity and mortality in children. The major limitations of cytogenetic tests currently used for the detection of such chromosomal rearrangements are low resolution and limited coverage of the genome. Thus, it is likely that children with MCA may have submicroscopic chromosomal rearrangements that are not detectable by current techniques. We report the use of a commercially available, oligonucleotide-based microarray for genome-wide analysis of copy number alterations. First, we validated the microarray in patients with known chromosomal rearrangements. Next, we identified previously undetected, de novo chromosomal deletions in patients with MCA who have had a normal high-resolution karyotype and subtelomeric fluorescence in situ hybridization (FISH) analysis. These findings indicate that high-density, oligonucleotide-based microarrays can be successfully used as tools for the detection of chromosomal rearrangement in clinical samples. Their higher resolution and commercial availability make this type of microarray highly desirable for application in the diagnosis of patients with multiple congenital defects.

摘要

染色体重排,如微缺失和中间重复,是许多人类遗传疾病的根本原因。这些疾病可能以多种先天性异常(MCA)的形式表现出来,而MCA是儿童发病和死亡的重要原因。目前用于检测此类染色体重排的细胞遗传学检测的主要局限性在于分辨率低和基因组覆盖范围有限。因此,患有MCA的儿童可能存在目前技术无法检测到的亚微观染色体重排。我们报告了使用一种市售的基于寡核苷酸的微阵列进行全基因组拷贝数改变分析的情况。首先,我们在已知染色体重排的患者中验证了该微阵列。接下来,我们在具有正常高分辨率核型和亚端粒荧光原位杂交(FISH)分析的MCA患者中鉴定出先前未检测到的新生染色体重排。这些发现表明,高密度、基于寡核苷酸的微阵列可以成功用作检测临床样本中染色体重排的工具。它们更高的分辨率和商业可用性使得这种类型的微阵列非常适合应用于患有多种先天性缺陷患者的诊断。

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