"single nucleotide polymorphism c 2161g" trang 12 - tải miễn phí từ tailieunhanh
Genetic polymorphism of the OPG gene associated with breast cancer

Genetic polymorphism of the OPG gene associated with breast cancer
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The relationship of Vascular endothelial growth factor gene polymorphisms and clinical outcome in advanced gastric cancer patients treated with FOLFOX: VEGF polymorphism in gastric cancer

The relationship of Vascular endothelial growth factor gene polymorphisms and clinical outcome in advanced gastric cancer patients treated with FOLFOX: VEGF polymorphism in gastric cancer
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Genetic oxidative stress variants and glioma risk in a Chinese population: A hospital-based case-control study

Genetic oxidative stress variants and glioma risk in a Chinese population: A hospital-based case-control study
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Variant effect predictions capture some aspects of deep mutational scanning experiments

Variant effect predictions capture some aspects of deep mutational scanning experiments
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Discovery of significant porcine SNPs for swine breed identification by a hybrid of information gain, genetic algorithm, and frequency feature selection technique

Discovery of significant porcine SNPs for swine breed identification by a hybrid of information gain, genetic algorithm, and frequency feature selection technique
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Loqusdb: Added value of an observations database of local genomic variation

Loqusdb: Added value of an observations database of local genomic variation
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Modeling allele-specific expression at the gene and SNP levels simultaneously by a Bayesian logistic mixed regression model

Modeling allele-specific expression at the gene and SNP levels simultaneously by a Bayesian logistic mixed regression model
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Sensitive detection of circular DNAs at single-nucleotide resolution using guided realignment of partially aligned reads

Sensitive detection of circular DNAs at single-nucleotide resolution using guided realignment of partially aligned reads
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Estimates of introgression as a function of pairwise distances

Estimates of introgression as a function of pairwise distances
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SV-Pop: Population-based structural variant analysis and visualization

SV-Pop: Population-based structural variant analysis and visualization
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Aggregation of experts: an application in the field of “interactomics” (detection of interactions on the basis of genomic data)

Aggregation of experts: an application in the field of “interactomics” (detection of interactions on the basis of genomic data)
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SMuRF: A novel tool to identify regulatory elements enriched for somatic point mutations

SMuRF: A novel tool to identify regulatory elements enriched for somatic point mutations
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Variant site strain typer (VaST): Efficient strain typing using a minimal number of variant genomic sites

Variant site strain typer (VaST): Efficient strain typing using a minimal number of variant genomic sites
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Mutational Signatures in Cancer (MuSiCa): A web application to implement mutational signatures analysis in cancer samples

Mutational Signatures in Cancer (MuSiCa): A web application to implement mutational signatures analysis in cancer samples
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Valection: Design optimization for validation and verification studies

Valection: Design optimization for validation and verification studies
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TNER: A novel background error suppression method for mutation detection in circulating tumor DNA

TNER: A novel background error suppression method for mutation detection in circulating tumor DNA
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Germline contamination and leakage in whole genome somatic single nucleotide variant detection

Germline contamination and leakage in whole genome somatic single nucleotide variant detection
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TIA: Algorithms for development of identity-linked SNP islands for analysis by massively parallel DNA sequencing

TIA: Algorithms for development of identity-linked SNP islands for analysis by massively parallel DNA sequencing
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BS-Seeker3: Ultrafast pipeline for bisulfite sequencing

BS-Seeker3: Ultrafast pipeline for bisulfite sequencing
4    47    1
An integrative approach to predicting the functional effects of small indels in non-coding regions of the human genome

An integrative approach to predicting the functional effects of small indels in non-coding regions of the human genome
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