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MHConstructor: A high-throughput, haplotype-informed solution to the MHC assembly challenge in disease genetics
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创建时间：
2024-02-01
相关数据集
ena-DATASET-MUGQIC-02-11-2018-16:39:30:386-128 - samples
Exome sequencing was performed on samples from patients 064, 105, and 8760, including the remission sample for 105. Exomes were captured using the Agilent SureSelect All Exon kit v5 kit and libraries
NIAID Data Ecosystem70
Additional file 11: of Meta-analysis of human gene expression in response to Mycobacterium tuberculosis infection reveals potential therapeutic targets
List of 58 Parkinsonâ s disease-associated genetic variants proximal to the 407 DEGs. (XLSX 12Â kb)
Figshare2018-01-10 更新50
Summary statistics data for "Genetic Analyses Support the Contribution of mRNA N6-methyladenosine (m6A) Modification to Human Diseases Heritability"
We included the summary statistics data associated with our manuscript "Genetic Analyses Support the Contribution of mRNA N6-methyladenosine (m6A) Modification to Human Diseases Heritability". We a
NIAID Data Ecosystem40
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Autism Center of Excellence (ACE II). Center for Common Disease Genomics (CCDG) Neuropsychiatric: Autism Center of Excellence (ACE II)
In this study, we address the enormous challenges common complex diseases pose for genomic analysis and the enormous opportunities surmounting them offers for advancing healthcare. The common genetic
NIAID Data Ecosystem60
Resulting 29 variants after filtration of exome data of a patient affected with nemaline myopathy.
An initial 86,333 variants were reduced to 250 using criteria on the variant level, which resulted in the 29 variants after exclusion of genes already ascribed to diseases and based on specificity of
NIAID Data Ecosystem40
