"single nucleotide polymorphism haplotype" trang 13 - tải miễn phí từ tailieunhanh
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    52    1
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    44    1
Eigen-Epistasis for detecting gene-gene interactions

Eigen-Epistasis for detecting gene-gene interactions
14    57    1
Whole genome SNP genotype piecemeal imputation

Whole genome SNP genotype piecemeal imputation
11    47    1
DiSNPindel: Improved intra-individual SNP and InDel detection in direct amplicon sequencing of a diploid

DiSNPindel: Improved intra-individual SNP and InDel detection in direct amplicon sequencing of a diploid
8    45    1
PGen: Large-scale genomic variations analysis workflow and browser in SoyKB

PGen: Large-scale genomic variations analysis workflow and browser in SoyKB
10    43    1
Representing and decomposing genomic structural variants as balanced integer flows on sequence graphs

Representing and decomposing genomic structural variants as balanced integer flows on sequence graphs
16    65    1
Afull Bayesian partitionmodelfor identifying hypo- and hyper-methylated loci from single nucleotide resolution sequencing data

Afull Bayesian partitionmodelfor identifying hypo- and hyper-methylated loci from single nucleotide resolution sequencing data
13    43    1
Impact of imputation methods on the amount of genetic variation captured by a single-nucleotide polymorphism panel in soybeans

Impact of imputation methods on the amount of genetic variation captured by a single-nucleotide polymorphism panel in soybeans
9    48    1
CerealsDB 3.0: Expansion of resources and data integration

CerealsDB 3.0: Expansion of resources and data integration
9    31    1
An investigation of causes of false positive single nucleotide polymorphisms using simulated reads from a small eukaryote genome

An investigation of causes of false positive single nucleotide polymorphisms using simulated reads from a small eukaryote genome
16    35    1
CINOEDV: A co-information based method for detecting and visualizing n-order epistatic interactions

CINOEDV: A co-information based method for detecting and visualizing n-order epistatic interactions
15    25    1
Equalizer reduces SNP bias in Affymetrix microarrays

Equalizer reduces SNP bias in Affymetrix microarrays
8    46    1
GESPA: Classifying nsSNPs to predict disease association

GESPA: Classifying nsSNPs to predict disease association
10    29    2
HaploPOP: A software that improves population assignment by combining markers into haplotypes

HaploPOP: A software that improves population assignment by combining markers into haplotypes
8    29    1
Performance of copy number variants detection based on whole‑genome sequencing by DNBSEQ platforms

Performance of copy number variants detection based on whole‑genome sequencing by DNBSEQ platforms
14    31    1
Joint haplotype assembly and genotype calling via sequential Monte Carlo algorithm

Joint haplotype assembly and genotype calling via sequential Monte Carlo algorithm
10    39    1
DRUMS: Disk Repository with Update Management and Select option for high throughput sequencing data

DRUMS: Disk Repository with Update Management and Select option for high throughput sequencing data
9    67    1
LDsplit: Screening for cis-regulatory motifs stimulating meiotic recombination hotspots by analysis of DNA sequence polymorphisms

LDsplit: Screening for cis-regulatory motifs stimulating meiotic recombination hotspots by analysis of DNA sequence polymorphisms
12    53    1
Comparison of genotype clustering tools with rare variants

Comparison of genotype clustering tools with rare variants
12    76    1