首页> 美国卫生研究院文献>Scientific Data >Whole-exome sequencing data of suicide victims who had suffered from major depressive disorder
【2h】

Whole-exome sequencing data of suicide victims who had suffered from major depressive disorder

机译:患有严重抑郁症的自杀受害者的全基因组测序数据

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Suicide is one of the leading causes of mortality worldwide; it causes the death of more than one million patients each year. Suicide is a complex, multifactorial phenotype with environmental and genetic factors contributing to the risk of the forthcoming suicide. These factors first generally lead to mental disorders, such as depression, schizophrenia and bipolar disorder, which then become the direct cause of suicide. Here we present a high quality dataset (including processed BAM and VCF files) gained from the high-throughput whole-exome Illumina sequencing of 23 suicide victims – all of whom had suffered from major depressive disorder - and 21 control patients to a depth of at least 40-fold coverage in both cohorts. We identified ~130,000 variants per sample and altogether 442,270 unique variants in the cohort of 44 samples. To our best knowledge, this is the first whole-exome sequencing dataset from suicide victims. We expect that this dataset provides useful information for genomic studies of suicide and depression, and also for the analysis of the Hungarian population.
机译:自杀是全球死亡的主要原因之一;每年导致超过一百万患者死亡。自杀是一种复杂的多因素表型,其环境和遗传因素导致即将自杀的风险。这些因素通常首先导致精神障碍,例如抑郁症,精神分裂症和躁郁症,然后成为自杀的直接原因。在这里,我们提供了高质量的数据集(包括处理后的BAM和VCF文件),该数据集是从23位自杀受害者(全部患有重性抑郁症)和21位对照患者的高通量全基因组Illumina测序中获得的,在两个队列中至少覆盖40倍。我们在44个样本的队列中,每个样本确定了约130,000个变体,以及总共442,270个独特变体。据我们所知,这是自杀受害者的第一个全基因组测序数据集。我们希望该数据集可为自杀和抑郁症的基因组研究提供有用的信息,并为匈牙利人口的分析提供有用的信息。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号