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PECONPI:一种用于揭示非综合征型感音神经性听力损失和其他遗传异质性疾病中致病性拷贝数变异的新型软件。

PECONPI: a novel software for uncovering pathogenic copy number variations in non-syndromic sensorineural hearing loss and other genetically heterogeneous disorders.

机构信息

Genomics and Computational Biology Graduate Group, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

出版信息

Am J Med Genet A. 2013 Sep;161A(9):2134-47. doi: 10.1002/ajmg.a.36038. Epub 2013 Jul 29.

DOI:10.1002/ajmg.a.36038
PMID:23897863
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3745548/
Abstract

This report describes an algorithm developed to predict the pathogenicity of copy number variants (CNVs) in large sample cohorts. CNVs (genomic deletions and duplications) are found in healthy individuals and in individuals with genetic diagnoses, and differentiation of these two classes of CNVs can be challenging and usually requires extensive manual curation. We have developed PECONPI, an algorithm to assess the pathogenicity of CNVs based on gene content and CNV frequency. This software was applied to a large cohort of patients with genetically heterogeneous non-syndromic hearing loss to score and rank each CNV based on its relative pathogenicity. Of 636 individuals tested, we identified the likely underlying etiology of the hearing loss in 14 (2%) of the patients (1 with a homozygous deletion, 7 with a deletion of a known hearing loss gene and a point mutation on the trans allele and 6 with a deletion larger than 1 Mb). We also identified two probands with smaller deletions encompassing genes that may be functionally related to their hearing loss. The ability of PECONPI to determine the pathogenicity of CNVs was tested on a second genetically heterogeneous cohort with congenital heart defects (CHDs). It successfully identified a likely etiology in 6 of 355 individuals (2%). We believe this tool is useful for researchers with large genetically heterogeneous cohorts to help identify known pathogenic causes and novel disease genes.

摘要

本报告描述了一种用于在大样本队列中预测拷贝数变异 (CNV) 致病性的算法。CNV(基因组缺失和重复)在健康个体和具有遗传诊断的个体中都有发现,区分这两类 CNV 具有挑战性,通常需要广泛的人工策管。我们开发了 PECONPI,这是一种基于基因内容和 CNV 频率评估 CNV 致病性的算法。该软件应用于一个具有遗传异质性的非综合征性听力损失的大患者队列,根据其相对致病性对每个 CNV 进行评分和排名。在 636 名接受测试的个体中,我们在 14 名(2%)患者中确定了听力损失的潜在病因(1 名患者为纯合性缺失,7 名患者为已知听力损失基因缺失和反义突变点,6 名患者缺失大于 1Mb)。我们还发现了两个包含可能与其听力损失相关的功能基因的较小缺失的先证者。PECONPI 确定 CNV 致病性的能力在第二个具有先天性心脏缺陷 (CHD) 的遗传异质性队列中进行了测试。它成功地在 355 名个体中的 6 名(2%)中确定了可能的病因。我们相信,对于具有大型遗传异质性队列的研究人员来说,该工具有助于识别已知的致病性原因和新的疾病基因。

相似文献

1
PECONPI: a novel software for uncovering pathogenic copy number variations in non-syndromic sensorineural hearing loss and other genetically heterogeneous disorders.PECONPI:一种用于揭示非综合征型感音神经性听力损失和其他遗传异质性疾病中致病性拷贝数变异的新型软件。
Am J Med Genet A. 2013 Sep;161A(9):2134-47. doi: 10.1002/ajmg.a.36038. Epub 2013 Jul 29.
2
Assessment of large copy number variants in patients with apparently isolated congenital left-sided cardiac lesions reveals clinically relevant genomic events.对明显孤立性先天性左侧心脏病变患者的大片段拷贝数变异进行评估,发现了具有临床相关性的基因组事件。
Am J Med Genet A. 2017 Aug;173(8):2176-2188. doi: 10.1002/ajmg.a.38309. Epub 2017 Jun 27.
3
Copy number variation as a genetic basis for heterotaxy and heterotaxy-spectrum congenital heart defects.拷贝数变异作为内脏异位和内脏异位谱先天性心脏病的遗传基础。
Philos Trans R Soc Lond B Biol Sci. 2016 Dec 19;371(1710). doi: 10.1098/rstb.2015.0406.
4
Microdeletions and microduplications in patients with congenital heart disease and multiple congenital anomalies.先天性心脏病和多发先天性畸形患者的微缺失和微重复
Congenit Heart Dis. 2011 Nov-Dec;6(6):592-602. doi: 10.1111/j.1747-0803.2011.00582.x. Epub 2011 Oct 20.
5
Frequency and clinical features of hearing loss caused by STRC deletions.STR*C 缺失导致的听力损失的频率和临床特征。
Sci Rep. 2019 Mar 13;9(1):4408. doi: 10.1038/s41598-019-40586-7.
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Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of -Associated Hearing Loss.中频听力损失是 - 相关听力损失的特征性临床特征。
Genes (Basel). 2019 Sep 16;10(9):715. doi: 10.3390/genes10090715.
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Copy number variants detection by microarray and multiplex ligation-dependent probe amplification in congenital heart diseases.通过微阵列和多重连接依赖性探针扩增检测先天性心脏病中的拷贝数变异。
J Biotechnol. 2019 Jun 20;299:86-95. doi: 10.1016/j.jbiotec.2019.04.025. Epub 2019 May 1.
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DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined with a Mutation Classification System.遗传性听力损失的DNA诊断:一种靶向重测序方法与突变分类系统相结合
Hum Mutat. 2016 Aug;37(8):812-9. doi: 10.1002/humu.22999. Epub 2016 May 6.
10
Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss.外显子组测序和全基因组拷贝数变异图谱揭示了与感音神经性遗传性听力损失的新关联。
BMC Genomics. 2014 Dec 20;15(1):1155. doi: 10.1186/1471-2164-15-1155.

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Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of -Associated Hearing Loss.中频听力损失是 - 相关听力损失的特征性临床特征。

本文引用的文献

1
Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment.全基因组 SNP 基因分型鉴定出 Stereocilin(STRC)基因是导致小儿双侧感音神经性听力损失的主要因素。
Am J Med Genet A. 2012 Feb;158A(2):298-308. doi: 10.1002/ajmg.a.34391. Epub 2011 Dec 6.
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A deleterious mutation in the LOXHD1 gene causes autosomal recessive hearing loss in Ashkenazi Jews.LOXHD1 基因中的有害突变导致阿什肯纳兹犹太人常染色体隐性遗传性耳聋。
Am J Med Genet A. 2011 May;155A(5):1170-2. doi: 10.1002/ajmg.a.33972. Epub 2011 Apr 4.
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Microdeletion of 17q22q23.2 encompassing TBX2 and TBX4 in a patient with congenital microcephaly, thyroid duct cyst, sensorineural hearing loss, and pulmonary hypertension.
Genes (Basel). 2019 Sep 16;10(9):715. doi: 10.3390/genes10090715.
4
The diagnostic yield of whole-exome sequencing targeting a gene panel for hearing impairment in The Netherlands.荷兰针对听力障碍基因panel的全外显子组测序的诊断率
Eur J Hum Genet. 2017 Feb;25(3):308-314. doi: 10.1038/ejhg.2016.182. Epub 2016 Dec 21.
5
Identification of copy number variants through whole-exome sequencing in autosomal recessive nonsyndromic hearing loss.通过全外显子组测序鉴定常染色体隐性非综合征性听力损失中的拷贝数变异
Genet Test Mol Biomarkers. 2014 Sep;18(9):658-61. doi: 10.1089/gtmb.2014.0121. Epub 2014 Jul 25.
患者患有先天性小头畸形、甲状腺导管囊肿、感音神经性听力损失和肺动脉高压,存在 17q22q23.2 区段的 TBX2 和 TBX4 缺失。
Am J Med Genet A. 2011 Feb;155A(2):418-23. doi: 10.1002/ajmg.a.33827. Epub 2011 Jan 13.
4
Accurate distinction of pathogenic from benign CNVs in mental retardation.准确区分精神发育迟滞中的致病性与良性 CNVs。
PLoS Comput Biol. 2010 Apr 22;6(4):e1000752. doi: 10.1371/journal.pcbi.1000752.
5
Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families.5 个新的遗传性听力损失基因座通过 SNP 基于纯合子谱在巴勒斯坦家庭中定位。
Eur J Hum Genet. 2010 Apr;18(4):407-13. doi: 10.1038/ejhg.2009.190. Epub 2009 Nov 4.
6
Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans.LOXHD1基因发生突变,该基因是一种在进化上保守的静纤毛蛋白,会破坏小鼠的毛细胞功能,并导致人类进行性听力丧失。
Am J Hum Genet. 2009 Sep;85(3):328-37. doi: 10.1016/j.ajhg.2009.07.017.
7
De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot.新生拷贝数变异鉴定出孤立性散发性法洛四联症中的新基因和基因座。
Nat Genet. 2009 Aug;41(8):931-5. doi: 10.1038/ng.415. Epub 2009 Jul 13.
8
High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.人类基因组中拷贝数变异的高分辨率图谱绘制与分析:临床及研究应用的数据资源。
Genome Res. 2009 Sep;19(9):1682-90. doi: 10.1101/gr.083501.108. Epub 2009 Jul 10.
9
A homozygous deletion of a normal variation locus in a patient with hearing loss from non-consanguineous parents.一名来自非近亲父母的听力损失患者中一个正常变异位点的纯合缺失。
J Med Genet. 2009 Jun;46(6):412-7. doi: 10.1136/jmg.2008.063685. Epub 2009 Feb 25.
10
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.罕见结构变异破坏精神分裂症神经发育通路中的多个基因。
Science. 2008 Apr 25;320(5875):539-43. doi: 10.1126/science.1155174. Epub 2008 Mar 27.