[Full Picture] Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts.

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Appears strongly imbalanced

Summary Analysis Research

1. 通过血液转录组测序和大型对照组，鉴定罕见疾病基因。

2. 研究团队使用了来自多个机构的数据，包括 Care4Rare Canada Consortium 和 Undiagnosed Diseases Network。

3. 这项研究有望帮助诊断罕见疾病，并为未来的治疗提供新的目标。

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Background information on the topic Current trends and developments Key players and stakeholders involved Challenges and obstacles faced Potential solutions and recommendations Future outlook and implications