"single nucleotide polymorphisms" trang 14 - tải miễn phí từ tailieunhanh
Identification of pathogen genomic variants through an integrated pipeline

Identification of pathogen genomic variants through an integrated pipeline
14    29    1
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    38    1
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    47    1
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    52    1
Identification of putative pathogenic SNPs implied in schizophrenia-associated miRNAs

Identification of putative pathogenic SNPs implied in schizophrenia-associated miRNAs
9    54    1
Using beta-binomial regression for high-precision differential methylation analysis in multifactor whole-genome bisulfite sequencing experiments

Using beta-binomial regression for high-precision differential methylation analysis in multifactor whole-genome bisulfite sequencing experiments
8    58    1
MAP-RSeq: Mayo Analysis Pipeline for RNA sequencing

MAP-RSeq: Mayo Analysis Pipeline for RNA sequencing
11    43    1
SubPatCNV: Approximate subspace pattern mining for mapping copy-number variations

SubPatCNV: Approximate subspace pattern mining for mapping copy-number variations
12    46    1
Identification of indels in next-generation sequencing data

Identification of indels in next-generation sequencing data
8    36    1
Fast and robust group-wise eQTL mapping using sparse graphical models

Fast and robust group-wise eQTL mapping using sparse graphical models
16    47    1
LincSNP: A database of linking disease-associated SNPs to human large intergenic non-coding RNAs

LincSNP: A database of linking disease-associated SNPs to human large intergenic non-coding RNAs
7    37    1
Determination of sample size for a multi-class classifier based on single-nucleotide polymorphisms: A volume under the surface approach

Determination of sample size for a multi-class classifier based on single-nucleotide polymorphisms: A volume under the surface approach
8    54    1
GVCBLUP: A computer package for genomic prediction and variance component estimation of additive and dominance effects

GVCBLUP: A computer package for genomic prediction and variance component estimation of additive and dominance effects
9    60    1
Performance analysis of novel methods for detecting epistasis

Performance analysis of novel methods for detecting epistasis
17    37    1
Identification of single nucleotide polymorphisms from the transcriptome of an organism with a whole genome duplication

Identification of single nucleotide polymorphisms from the transcriptome of an organism with a whole genome duplication
10    26    1
Snp-search: Simple processing, manipulation and searching of SNPs from high-throughput sequencing

Snp-search: Simple processing, manipulation and searching of SNPs from high-throughput sequencing
8    36    1
Critical assessment of coalescent simulators in modeling recombination hotspots in genomic sequences

Critical assessment of coalescent simulators in modeling recombination hotspots in genomic sequences
14    36    1
SynTView - an interactive multi-view genome browser for next-generation comparative microorganism genomics

SynTView - an interactive multi-view genome browser for next-generation comparative microorganism genomics
9    40    1
Large-scale multiple testing in genome-wide association studies via region-specific hidden Markov models

Large-scale multiple testing in genome-wide association studies via region-specific hidden Markov models
12    65    1
Snpdat: Easy and rapid annotation of results from de novo snp discovery projects for model and non-model organisms

Snpdat: Easy and rapid annotation of results from de novo snp discovery projects for model and non-model organisms
6    26    1