"Genotype phenotype" trang 1 - tải miễn phí từ tailieuXANH
Linking genotype to phenotype in multiomics data of small sample

Linking genotype to phenotype in multiomics data of small sample
11    239    1
Rapid screening for phenotype-genotype associations by linear transformations of genomic evaluations

Rapid screening for phenotype-genotype associations by linear transformations of genomic evaluations
11    81    0
Báo cáo y học:

Báo cáo y học: " Cluster analysis in severe emphysema subjects using phenotype and genotype data: an exploratory investigation"
9    46    0
Báo cáo y học:

Báo cáo y học: " XGAP: a uniform and extensible data model and software platform for genotype and phenotype experiments"
1    47    0
Báo cáo khoa học: Functional and structural characterization of novel mutations and genotype–phenotype correlation in 51 phenylalanine hydroxylase deficient families from Southern Italy

Báo cáo khoa học: Functional and structural characterization of novel mutations and genotype–phenotype correlation in 51 phenylalanine hydroxylase deficient families from Southern Italy
12    37    0
Báo cáo khóa học: Genetic defects in fatty acid b-oxidation and acyl-CoA dehydrogenases Molecular pathogenesis and genotype–phenotype relationships

Báo cáo khóa học: Genetic defects in fatty acid b-oxidation and acyl-CoA dehydrogenases Molecular pathogenesis and genotype–phenotype relationships
13    55    0
Báo cáo khoa học: New insights into Fragile X syndrome Relating genotype to phenotype at the molecular level

Báo cáo khoa học: New insights into Fragile X syndrome Relating genotype to phenotype at the molecular level
1    36    0
Lecture Biology - Chapter 12: From DNA to protein: genotype to phenotype

Lecture Biology - Chapter 12: From DNA to protein: genotype to phenotype
106    62    0
A comprehensive overview of the cystic fibrosis on the island of São Miguel (Azores, Portugal)

A comprehensive overview of the cystic fibrosis on the island of São Miguel (Azores, Portugal)
7    44    0
Clinical and genetic characteristics of patients with fatty acid oxidation disorders identified by newborn screening

Clinical and genetic characteristics of patients with fatty acid oxidation disorders identified by newborn screening
7    45    0
Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: A case report and review of the literature

Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: A case report and review of the literature
7    71    0
Phenotypic and genetic characterization of a cohort of pediatric wilson disease patients

Phenotypic and genetic characterization of a cohort of pediatric wilson disease patients
11    62    0
Genetic parameters for yield and yield components in F1 hybrids and parents of bell pepper

Genetic parameters for yield and yield components in F1 hybrids and parents of bell pepper
5    81    0
A pharmacogenetic pilot study reveals MTHFR, DRD3, and MDR1 polymorphisms as biomarker candidates for slow atorvastatin metabolizers

A pharmacogenetic pilot study reveals MTHFR, DRD3, and MDR1 polymorphisms as biomarker candidates for slow atorvastatin metabolizers
13    65    0
Increased coagulation activity and genetic polymorphisms in the F5, F10 and EPCR genes are associated with breast cancer: A case-control study

Increased coagulation activity and genetic polymorphisms in the F5, F10 and EPCR genes are associated with breast cancer: A case-control study
11    62    0
An integrative methodology based on protein-protein interaction networks for identification and functional annotation of disease-relevant genes applied to channelopathies

An integrative methodology based on protein-protein interaction networks for identification and functional annotation of disease-relevant genes applied to channelopathies
13    57    0
In silico analysis of missense mutations in exons 1–5 of the F9 gene that cause hemophilia B

In silico analysis of missense mutations in exons 1–5 of the F9 gene that cause hemophilia B
13    47    0
Predicting bacterial resistance from whole-genome sequences using k-mers and stability selection

Predicting bacterial resistance from whole-genome sequences using k-mers and stability selection
11    44    0
GenIO: A phenotype-genotype analysis web server for clinical genomics of rare diseases

GenIO: A phenotype-genotype analysis web server for clinical genomics of rare diseases
6    49    0
Using variant databases for variant prioritization and to detect erroneous genotype-phenotype associations

Using variant databases for variant prioritization and to detect erroneous genotype-phenotype associations
10    108    0
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