"next generation sequencing" trang 15 - tải miễn phí từ tailieuXANH
Genetic heterogeneity of actionable genes between primary and metastatic tumor in lung adenocarcinoma

Genetic heterogeneity of actionable genes between primary and metastatic tumor in lung adenocarcinoma
9    68    0
Clinical detection and categorization of uncommon and concomitant mutations involving BRAF

Clinical detection and categorization of uncommon and concomitant mutations involving BRAF
10    70    0
Advantages of a next generation sequencing targeted approach for the molecular diagnosis of retinoblastoma

Advantages of a next generation sequencing targeted approach for the molecular diagnosis of retinoblastoma
9    61    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
Plasma-based longitudinal mutation monitoring as a potential predictor of disease progression in subjects with adenocarcinoma in advanced non-small cell lung cancer

Plasma-based longitudinal mutation monitoring as a potential predictor of disease progression in subjects with adenocarcinoma in advanced non-small cell lung cancer
9    48    0
Multiple gene aberrations and breast cancer: Lessons from super-responders

Multiple gene aberrations and breast cancer: Lessons from super-responders
6    53    0
MicroRNA-223 is a novel negative regulator of HSP90B1 in CLL

MicroRNA-223 is a novel negative regulator of HSP90B1 in CLL
9    52    0
No significant viral transcription detected in whole breast cancer transcriptomes

No significant viral transcription detected in whole breast cancer transcriptomes
9    45    0
Exome profiling of primary, metastatic and recurrent ovarian carcinomas in a BRCA1-positive patient

Exome profiling of primary, metastatic and recurrent ovarian carcinomas in a BRCA1-positive patient
11    56    0
ARTDeco: Automatic readthrough transcription detection

ARTDeco: Automatic readthrough transcription detection
22    112    0
CNV Radar: An improved method for somatic copy number alteration characterization in oncology

CNV Radar: An improved method for somatic copy number alteration characterization in oncology
18    66    0
Magic-BLAST, an accurate RNA-seq aligner for long and short reads

Magic-BLAST, an accurate RNA-seq aligner for long and short reads
19    48    0
Guide for library design and bias correction for large-scale transcriptome studies using highly multiplexed RNAseq methods

Guide for library design and bias correction for large-scale transcriptome studies using highly multiplexed RNAseq methods
9    57    0
RACS: Rapid analysis of ChIP-Seq data for contig based genomes

RACS: Rapid analysis of ChIP-Seq data for contig based genomes
17    58    0
Sensitive detection of circular DNAs at single-nucleotide resolution using guided realignment of partially aligned reads

Sensitive detection of circular DNAs at single-nucleotide resolution using guided realignment of partially aligned reads
9    49    0
NeoPredPipe: High-throughput neoantigen prediction and recognition potential pipeline

NeoPredPipe: High-throughput neoantigen prediction and recognition potential pipeline
6    45    0
Comparison of kNN and k-means optimization methods of reference set selection for improved CNV callers performance

Comparison of kNN and k-means optimization methods of reference set selection for improved CNV callers performance
10    64    0
Polymorphic edge detection (PED): Two efficient methods of polymorphism detection from next-generation sequencing data

Polymorphic edge detection (PED): Two efficient methods of polymorphism detection from next-generation sequencing data
12    69    0
NIPTeR: An R package for fast and accurate trisomy prediction in non-invasive prenatal testing

NIPTeR: An R package for fast and accurate trisomy prediction in non-invasive prenatal testing
5    47    0
Shambhala: A platform-agnostic data harmonizer for gene expression data

Shambhala: A platform-agnostic data harmonizer for gene expression data
10    60    0
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