"single nucleotide polymorphism array" trang 13 - tải miễn phí từ tailieuXANH
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    53    0
PGen: Large-scale genomic variations analysis workflow and browser in SoyKB

PGen: Large-scale genomic variations analysis workflow and browser in SoyKB
10    48    0
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    68    0
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    88    0
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    59    0
CerealsDB 3.0: Expansion of resources and data integration

CerealsDB 3.0: Expansion of resources and data integration
9    70    0
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    64    0
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    62    0
Equalizer reduces SNP bias in Affymetrix microarrays

Equalizer reduces SNP bias in Affymetrix microarrays
8    35    0
GESPA: Classifying nsSNPs to predict disease association

GESPA: Classifying nsSNPs to predict disease association
10    61    0
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    47    0
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    67    0
Joint haplotype assembly and genotype calling via sequential Monte Carlo algorithm

Joint haplotype assembly and genotype calling via sequential Monte Carlo algorithm
10    58    0
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    55    0
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    87    0
Comparison of genotype clustering tools with rare variants

Comparison of genotype clustering tools with rare variants
12    63    0
Identification of pathogen genomic variants through an integrated pipeline

Identification of pathogen genomic variants through an integrated pipeline
14    57    0
Information compression exploits patterns of genome composition to discriminate populations and highlight regions of evolutionary interest

Information compression exploits patterns of genome composition to discriminate populations and highlight regions of evolutionary interest
21    61    0
A comprehensive study of small non-frameshift insertions/deletions in proteins and prediction of their phenotypic effects by a machine learning method (KD4i)

A comprehensive study of small non-frameshift insertions/deletions in proteins and prediction of their phenotypic effects by a machine learning method (KD4i)
20    65    0
Effective filtering strategies to improve data quality from population-based whole exome sequencing studies

Effective filtering strategies to improve data quality from population-based whole exome sequencing studies
15    67    0
Đã phát hiện trình chặn quảng cáo AdBlock
Trang web này phụ thuộc vào doanh thu từ số lần hiển thị quảng cáo để tồn tại. Vui lòng tắt trình chặn quảng cáo của bạn hoặc tạm dừng tính năng chặn quảng cáo cho trang web này.