"single nucleotide polymorphisms" trang 12 - tải miễn phí từ tailieuXANH
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
28    54    0
Loqusdb: Added value of an observations database of local genomic variation

Loqusdb: Added value of an observations database of local genomic variation
10    43    0
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
13    53    0
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
9    49    0
Estimates of introgression as a function of pairwise distances

Estimates of introgression as a function of pairwise distances
11    160    0
SV-Pop: Population-based structural variant analysis and visualization

SV-Pop: Population-based structural variant analysis and visualization
4    72    0
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)
15    60    0
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
5    46    0
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
13    68    0
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
6    67    0
Valection: Design optimization for validation and verification studies

Valection: Design optimization for validation and verification studies
11    89    0
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
7    92    0
Germline contamination and leakage in whole genome somatic single nucleotide variant detection

Germline contamination and leakage in whole genome somatic single nucleotide variant detection
9    49    0
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
13    51    0
BS-Seeker3: Ultrafast pipeline for bisulfite sequencing

BS-Seeker3: Ultrafast pipeline for bisulfite sequencing
4    52    0
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
8    46    0
KNN-MDR: A learning approach for improving interactions mapping performances in genome wide association studies

KNN-MDR: A learning approach for improving interactions mapping performances in genome wide association studies
12    67    0
Genomic prediction with epistasis models: on the marker-coding-dependent performance of the extended GBLUP and properties of the categorical epistasis model (CE)

Genomic prediction with epistasis models: on the marker-coding-dependent performance of the extended GBLUP and properties of the categorical epistasis model (CE)
16    51    0
Eigen-Epistasis for detecting gene-gene interactions

Eigen-Epistasis for detecting gene-gene interactions
14    56    0
Whole genome SNP genotype piecemeal imputation

Whole genome SNP genotype piecemeal imputation
11    95    0
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