"next generation sequencing" trang 5 - tải miễn phí từ tailieuXANH
Deduction of novel genes potentially involved in upper tract urothelial carcinoma using next generation sequencing and bioinformatics approaches

Deduction of novel genes potentially involved in upper tract urothelial carcinoma using next generation sequencing and bioinformatics approaches
13    64    0
Malignant acrospiroma: A case report in the era of next generation sequencing

Malignant acrospiroma: A case report in the era of next generation sequencing
4    43    0
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    98    0
A new massively parallel nanoball sequencing platform for whole exome research

A new massively parallel nanoball sequencing platform for whole exome research
9    61    0
Variant detection sensitivity and biases in whole genome and exome sequencing

Variant detection sensitivity and biases in whole genome and exome sequencing
11    71    0
LRScaf: Improving draft genomes using long noisy reads

LRScaf: Improving draft genomes using long noisy reads
12    55    2
Preliminary results on the whole genome analysis of a Vietnamese individual

Preliminary results on the whole genome analysis of a Vietnamese individual
5    54    0
Whole genome sequencing reveals complexity in both HPV sequences present and HPV integrations in HPV-positive oropharyngeal squamous cell carcinomas

Whole genome sequencing reveals complexity in both HPV sequences present and HPV integrations in HPV-positive oropharyngeal squamous cell carcinomas
15    66    0
Precision oncology using a limited number of cells: Optimization of whole genome amplification products for sequencing applications

Precision oncology using a limited number of cells: Optimization of whole genome amplification products for sequencing applications
12    120    0
Comparative study of whole exome sequencing-based copy number variation detection tools

Comparative study of whole exome sequencing-based copy number variation detection tools
10    69    0
SCSIM: Jointly simulating correlated single-cell and bulk next-generation DNA sequencing data

SCSIM: Jointly simulating correlated single-cell and bulk next-generation DNA sequencing data
10    69    0
Quantification of experimentally induced nucleotide conversions in high-throughput sequencing datasets

Quantification of experimentally induced nucleotide conversions in high-throughput sequencing datasets
16    49    0
SEQprocess: A modularized and customizable pipeline framework for NGS processing in R package

SEQprocess: A modularized and customizable pipeline framework for NGS processing in R package
7    75    0
DrImpute: Imputing dropout events in single cell RNA sequencing data

DrImpute: Imputing dropout events in single cell RNA sequencing data
10    57    0
A study on fast calling variants from nextgeneration sequencing data using decision tree

A study on fast calling variants from nextgeneration sequencing data using decision tree
14    68    0
MPD: Multiplex primer design for nextgeneration targeted sequencing

MPD: Multiplex primer design for nextgeneration targeted sequencing
5    75    0
Statistical method to compare massive parallel sequencing pipelines

Statistical method to compare massive parallel sequencing pipelines
11    62    0
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    62    0
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    88    0
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    75    0
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