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NGS-Integrator: An efficient tool for combining multiple NGS data tracks using minimum Bayes’ factors

NGS-Integrator: An efficient tool for combining multiple NGS data tracks using minimum Bayes’ factors
7    192    1
Targeted capture-based NGS is superior to multiplex PCR-based NGS for hereditary BRCA1 and BRCA2 gene analysis in FFPE tumor samples

Targeted capture-based NGS is superior to multiplex PCR-based NGS for hereditary BRCA1 and BRCA2 gene analysis in FFPE tumor samples
15    52    0
Khảo sát một số đột biến gen Beta Globin hiếm gặp ở người Việt Nam bằng phương pháp NGS

Khảo sát một số đột biến gen Beta Globin hiếm gặp ở người Việt Nam bằng phương pháp NGS
9    50    0
Use of the QIAGEN GeneReader NGS system for detection of KRAS mutations, validated by the QIAGEN Therascreen PCR kit and alternative NGS platform

Use of the QIAGEN GeneReader NGS system for detection of KRAS mutations, validated by the QIAGEN Therascreen PCR kit and alternative NGS platform
8    108    0
NEAT: A framework for building fully automated NGS pipelines and analyses

NEAT: A framework for building fully automated NGS pipelines and analyses
9    86    0
SeqPurge: Highly-sensitive adapter trimming for paired-end NGS data

SeqPurge: Highly-sensitive adapter trimming for paired-end NGS data
7    71    0
Comprehensive kinome NGS targeted expression profiling by KING-REX

Comprehensive kinome NGS targeted expression profiling by KING-REX
12    58    1
Bead-linked transposomes enable a normalization-free workflow for NGS library preparation

Bead-linked transposomes enable a normalization-free workflow for NGS library preparation
16    230    1
Next generation sequencing expression profiling of mitochondrial subunits in men with Klinefelter syndrome

Next generation sequencing expression profiling of mitochondrial subunits in men with Klinefelter syndrome
5    46    0
An application of NGS for WDR36 gene in Taiwanese patients with juvenile-onset open-angle glaucoma

An application of NGS for WDR36 gene in Taiwanese patients with juvenile-onset open-angle glaucoma
6    46    0
The next generation of biopanning: Next gen sequencing improves analysis of bacterial display libraries

The next generation of biopanning: Next gen sequencing improves analysis of bacterial display libraries
12    47    0
NexGenEx-Tom: A gene expression platform to investigate the functionalities of the tomato genome

NexGenEx-Tom: A gene expression platform to investigate the functionalities of the tomato genome
13    63    0
Technical advance in targeted NGS analysis enables identification of lung cancer riskassociated low frequency TP53, PIK3CA, and BRAF mutations in airway epithelial cells

Technical advance in targeted NGS analysis enables identification of lung cancer riskassociated low frequency TP53, PIK3CA, and BRAF mutations in airway epithelial cells
14    69    0
Different next-generation sequencing pipelines based detection of tumor DNA in cerebrospinal fluid of lung adenocarcinoma cancer patients with leptomeningeal metastases

Different next-generation sequencing pipelines based detection of tumor DNA in cerebrospinal fluid of lung adenocarcinoma cancer patients with leptomeningeal metastases
8    69    0
An approach to forecast human cancer by profiling microRNA expressions from NGS data

An approach to forecast human cancer by profiling microRNA expressions from NGS data
9    45    0
Validation of an NGS mutation detection panel for melanoma

Validation of an NGS mutation detection panel for melanoma
7    65    0
Cost-effectiveness analysis comparing companion diagnostic tests for EGFR, ALK, and ROS1 versus next-generation sequencing (NGS) in advanced adenocarcinoma lung cancer patients

Cost-effectiveness analysis comparing companion diagnostic tests for EGFR, ALK, and ROS1 versus next-generation sequencing (NGS) in advanced adenocarcinoma lung cancer patients
10    71    0
RepAHR: An improved approach for de novo repeat identification by assembly of the high‑frequency reads

RepAHR: An improved approach for de novo repeat identification by assembly of the high‑frequency reads
24    50    0
DNAscan: Personal computer compatible NGS analysis, annotation and visualisation

DNAscan: Personal computer compatible NGS analysis, annotation and visualisation
10    53    0
SRAssembler: Selective Recursive local Assembly of homologous genomic regions

SRAssembler: Selective Recursive local Assembly of homologous genomic regions
13    56    0
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