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Mutations identified in the SMAD3 gene.
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创建时间:
2015-12-02
相关数据集
Additional file 5 of Publisher Correction: Frugal alignment-free identification of FLT3-internal tandem duplications with FiLT3r
Additional file 5. supp file 5: results-small-k.xlsx.
DataCite Commons2024-08-13 更新110
Additional file 2 of InMut-finder: a software tool for insertion identification in mutagenesis using Nanopore long reads
Additional file 2: Supplemental Table S1. All insertion sites identified in one soybean Ds mutant. Supplemental Table S2. Three selected insertion sites and primer sequences for PCR validation for the
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Discovery of Candidate Disease Genes in ENU–Induced Mouse Mutants by Large-Scale Sequencing, Including a Splice-Site Mutation in Nucleoredoxin
An accurate and precisely annotated genome assembly is a fundamental requirement for functional genomic analysis. Here, the complete DNA sequence and gene annotation of mouse Chromosome 11 was used to
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Identification of a mutation related to fatal Foal Immunodeficiency Syndrome in the Fell and Dales pony
The lethal Mendelian disease Foal Immunodeficiency Syndrome (FIS), which manifests as B-lymphocyte immunodeficiency and progressive anaemia (Scholes et al. 1998), is a substantial threat to Fell and D
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Genetic analysis of one family with oligodontia and ectodermal dysplasia
Two members of this family is affected by ectodermal dysplasia. The goal is to identify the pathogenic mutations.
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