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资源简介：
Screening for genes associated with deafness
应用场景：
创建时间：
2020-05-16
相关数据集
Variants of OTOF and PJVK Genes in Chinese Patients with Auditory Neuropathy Spectrum Disorder
BackgroundMutations in OTOF and PJVK genes cause DFNB9 and DFNB59 types of hearing loss, respectively. The patients carrying pathogenic mutations in either of these genes may show the typical phenotyp
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PCNT point mutations and familial intracranial aneurysms
Objective: To identify novel genes involved in the etiology of intracranial aneurysms (IA) and / or subarachnoid hemorrhages (SAH) using whole exome sequencing. Methods. In the present study we perfor
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Additional file 2: of Evaluation of three read-depth based CNV detection tools using whole-exome sequencing data
Details of all 17ďťż1 variants detected by CMA. (XLS 90Â kb)
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Panicum virgatum exome capture - SAP-15-12. Panicum virgatum cultivar:SAP-15-12
Switchgrass diversity analysis via exome sequencing
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Hereditary Hearing Loss SNP-Microarray Pilot Study. Hereditary Hearing Loss SNP-Microarray Pilot Study
Objectives: Despite recent advancements in diagnostic tools, the genomic landscape of hereditary hearing loss remains largely uncharacterized. One strategy to understand genome-wide aberrations includ
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