"Sequencing method" trang 1 - tải miễn phí từ tailieuXANH
Detection of 16s rRNA and 23s rRNA gene mutations in multidrug resistant salmonella serovars isolated from different sources using RNA sequencing method

Detection of 16s rRNA and 23s rRNA gene mutations in multidrug resistant salmonella serovars isolated from different sources using RNA sequencing method
8    105    2
ATRAM - automated target restricted assembly method: A fast method for assembling loci across divergent taxa from next-generation sequencing data

ATRAM - automated target restricted assembly method: A fast method for assembling loci across divergent taxa from next-generation sequencing data
7    68    0
Modeling of shotgun sequencing of DNA plasmids using experimental and theoretical approaches

Modeling of shotgun sequencing of DNA plasmids using experimental and theoretical approaches
13    54    0
Statistical method to compare massive parallel sequencing pipelines

Statistical method to compare massive parallel sequencing pipelines
11    62    0
A computational method for genotype calling in family-based sequencing data

A computational method for genotype calling in family-based sequencing data
13    62    0
TagDust2: A generic method to extract reads from sequencing data

TagDust2: A generic method to extract reads from sequencing data
8    60    0
ALPHLARD: A Bayesian method for analyzing HLA genes from whole genome sequence data

ALPHLARD: A Bayesian method for analyzing HLA genes from whole genome sequence data
11    36    1
ReSeq simulates realistic Illumina high-throughput sequencing data

ReSeq simulates realistic Illumina high-throughput sequencing data
37    159    1
Measuring sequencer size bias using REcount: A novel method for highly accurate Illumina sequencing-based quantification

Measuring sequencer size bias using REcount: A novel method for highly accurate Illumina sequencing-based quantification
17    16    1
A simple method to estimate the in-house limit of detection for genetic mutations with low allele frequencies in whole-exome sequencing analysis by next-generation sequencing

A simple method to estimate the in-house limit of detection for genetic mutations with low allele frequencies in whole-exome sequencing analysis by next-generation sequencing
10    7    1
Detecting familial defective apolipoprotein B-100 R3500Q in Vietnamese patients by PCR-sequencing

Detecting familial defective apolipoprotein B-100 R3500Q in Vietnamese patients by PCR-sequencing
8    43    0
A simple method for semi-random DNA amplicon fragmentation using the methylation-dependent restriction enzyme MspJI

A simple method for semi-random DNA amplicon fragmentation using the methylation-dependent restriction enzyme MspJI
13    63    0
Evaluation of the role of culture, pcr, and sequencing in the diagnosis of spontaneous bacterial peritonitis in patients with ascites

Evaluation of the role of culture, pcr, and sequencing in the diagnosis of spontaneous bacterial peritonitis in patients with ascites
11    76    0
The impact of RNA extraction method on accurate RNA sequencing from formalinfixed paraffin-embedded tissues

The impact of RNA extraction method on accurate RNA sequencing from formalinfixed paraffin-embedded tissues
12    64    0
SeqCNV: A novel method for identification of copy number variations in targeted next-generation sequencing data

SeqCNV: A novel method for identification of copy number variations in targeted next-generation sequencing data
9    57    0
Analysis of amplicon-based NGS data from neurological disease gene panels: A new method for allele drop-out management

Analysis of amplicon-based NGS data from neurological disease gene panels: A new method for allele drop-out management
12    66    0
Odintifier - A computational method for identifying insertions of organellar origin from modern and ancient high-throughput sequencing data based on haplotype phasing

Odintifier - A computational method for identifying insertions of organellar origin from modern and ancient high-throughput sequencing data based on haplotype phasing
13    45    0
Reference-free compression of high throughput sequencing data with a probabilistic de Bruijn graph

Reference-free compression of high throughput sequencing data with a probabilistic de Bruijn graph
14    40    0
DAFS: A data-adaptive flag method for RNA-sequencing data to differentiate genes with low and high expression

DAFS: A data-adaptive flag method for RNA-sequencing data to differentiate genes with low and high expression
11    65    0
An integrative method to normalize RNA-Seq data

An integrative method to normalize RNA-Seq data
11    62    0
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