"next generation sequencing" trang 6 - tải miễn phí từ tailieunhanh
Reproducibility of Illumina platform deep sequencing errors allows accurate determination of DNA barcodes in cells

Reproducibility of Illumina platform deep sequencing errors allows accurate determination of DNA barcodes in cells
16    79    1
SPARTA: Simple program for automated reference-based bacterial RNA-seq transcriptome analysis

SPARTA: Simple program for automated reference-based bacterial RNA-seq transcriptome analysis
4    68    1
Using single cell sequencing data to model the evolutionary history of a tumor

Using single cell sequencing data to model the evolutionary history of a tumor
13    52    1
QTrim: A novel tool for the quality trimming of sequence reads generated using the Roche/454 sequencing platform

QTrim: A novel tool for the quality trimming of sequence reads generated using the Roche/454 sequencing platform
6    34    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
TagDust2: A generic method to extract reads from sequencing data

TagDust2: A generic method to extract reads from sequencing data
8    31    1
PASTA: Splice junction identification from RNA-Sequencing data

PASTA: Splice junction identification from RNA-Sequencing data
11    43    1
A multiple-alignment based primer design algorithm for genetically highly variable DNA targets

A multiple-alignment based primer design algorithm for genetically highly variable DNA targets
9    62    1
Analytical validation of the Percepta genomic sequencing classifier; an RNA next generation sequencing assay for the assessment of Lung Cancer risk of suspicious pulmonary nodules

Analytical validation of the Percepta genomic sequencing classifier; an RNA next generation sequencing assay for the assessment of Lung Cancer risk of suspicious pulmonary nodules
10    29    1
RNA sequencing: A potent transcription profiling tool

RNA sequencing: A potent transcription profiling tool
15    52    1
Characterizing glycosyltransferases by a combination of sequencing platforms applied to the leaf tissues of Stevia rebaudiana

Characterizing glycosyltransferases by a combination of sequencing platforms applied to the leaf tissues of Stevia rebaudiana
16    37    1
Dual indexed library design enables compatibility of in-Drop single-cell RNAsequencing with exAMP chemistry sequencing platforms

Dual indexed library design enables compatibility of in-Drop single-cell RNAsequencing with exAMP chemistry sequencing platforms
15    24    2
Combining next-generation sequencing and single-molecule sequencing to explore brown plant hopper responses to contrasting genotypes of japonica rice

Combining next-generation sequencing and single-molecule sequencing to explore brown plant hopper responses to contrasting genotypes of japonica rice
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Comparative transcriptome analyses of genes involved in sulforaphane metabolism at different treatment in Chinese kale using full-length transcriptome sequencing

Comparative transcriptome analyses of genes involved in sulforaphane metabolism at different treatment in Chinese kale using full-length transcriptome sequencing
13    34    1
Exploring the unmapped DNA and RNA reads in a songbird genome

Exploring the unmapped DNA and RNA reads in a songbird genome
12    52    1
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    44    1
Whole exome sequencing in the rat

Whole exome sequencing in the rat
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Detailed evaluation of cancer sequencing pipelines in different microenvironments and heterogeneity levels

Detailed evaluation of cancer sequencing pipelines in different microenvironments and heterogeneity levels
13    53    1
Depletion of Abundant Sequences by Hybridization (DASH): Using Cas9 to remove unwanted high-abundance species in sequencing libraries and molecular counting applications

Depletion of Abundant Sequences by Hybridization (DASH): Using Cas9 to remove unwanted high-abundance species in sequencing libraries and molecular counting applications
13    14    1
Streamlined analysis of duplex sequencing data with Du Novo

Streamlined analysis of duplex sequencing data with Du Novo
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