Sordaria humana Genome sequencing and assembly. Sordaria humana
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New variant on TNAC1, RLS Syndrome
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2020-08-03
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Quantitative effect of each additional HCV genetic variation that is unique to the marked or poor day 28 response classes on eventual treatment outcome a.
aComparing SVR (sustained viral response) vs. NR (non-response). bFor example, a relative risk of 1.18 for E1 in genotype 1a indicates that for one additional marked/poor response-specific unique vari
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Additional file 1 of Protective PLCG2 variants associate with a delayed onset of Alzheimer’s disease among heterozygous APOE ε4 carriers
Supplementary Material 1. FinnGen Banner Sep2025.
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Association of Specific ACE2 and TMPRSS2 Variants with Circulatory Cytokines of COVID-19 Emirati Patients
The COVID-19 pandemic represented one of the most significant challenges to researchers and healthcare providers. Several factors determine the disease severity, whereas none alone can explain the tre
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Genomic Hypomethylation in the Human Germline Associates with Selective Structural Mutability in the Human Genome
The hotspots of structural polymorphisms and structural mutability in the human genome remain to be explained mechanistically. We examine associations of structural mutability with germline DNA methyl
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The molecular and clinical details of variants identified in EB patients.
The molecular and clinical details of variants identified in EB patients.
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