"next generation sequencing" trang 8 - tải miễn phí từ tailieunhanh
The characteristics of ctDNA reveal the high complexity in matching the corresponding tumor tissues

The characteristics of ctDNA reveal the high complexity in matching the corresponding tumor tissues
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Application of amplicon-based targeted sequencing with the molecular barcoding system to detect uncommon minor EGFR mutations in patients with treatment-naïve lung adenocarcinoma

Application of amplicon-based targeted sequencing with the molecular barcoding system to detect uncommon minor EGFR mutations in patients with treatment-naïve lung adenocarcinoma
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Mutation allele frequency threshold does not affect prognostic analysis using nextgeneration sequencing in oral squamous cell carcinoma

Mutation allele frequency threshold does not affect prognostic analysis using nextgeneration sequencing in oral squamous cell carcinoma
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Tracking the origin of simultaneous endometrial and ovarian cancer by nextgeneration sequencing – a case report

Tracking the origin of simultaneous endometrial and ovarian cancer by nextgeneration sequencing – a case report
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Clinical application of genomic profiling to find druggable targets for adolescent and young adult (AYA) cancer patients with metastasis

Clinical application of genomic profiling to find druggable targets for adolescent and young adult (AYA) cancer patients with metastasis
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Whole exome sequencing of microdissected splenic marginal zone lymphoma: A study to discover novel tumor-specific mutations

Whole exome sequencing of microdissected splenic marginal zone lymphoma: A study to discover novel tumor-specific mutations
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Determining the origin of synchronous multifocal bladder cancer by exome sequencing

Determining the origin of synchronous multifocal bladder cancer by exome sequencing
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Targeted deep sequencing of mucinous ovarian tumors reveals multiple overlapping RAS-pathway activating mutations in borderline and cancerous neoplasms

Targeted deep sequencing of mucinous ovarian tumors reveals multiple overlapping RAS-pathway activating mutations in borderline and cancerous neoplasms
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Tumor evolution and intratumor heterogeneity of an epithelial ovarian cancer investigated using next-generation sequencing

Tumor evolution and intratumor heterogeneity of an epithelial ovarian cancer investigated using next-generation sequencing
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Prognostic prediction of glioblastoma by quantitative assessment of the methylation status of the entire MGMT promoter region

Prognostic prediction of glioblastoma by quantitative assessment of the methylation status of the entire MGMT promoter region
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A big data approach to metagenomics for all-food-sequencing

A big data approach to metagenomics for all-food-sequencing
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PyBSASeq: A simple and effective algorithm for bulked segregant analysis with wholegenome sequencing data

PyBSASeq: A simple and effective algorithm for bulked segregant analysis with wholegenome sequencing data
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GenePy - a score for estimating gene pathogenicity in individuals using nextgeneration sequencing data

GenePy - a score for estimating gene pathogenicity in individuals using nextgeneration sequencing data
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FastProNGS: Fast preprocessing of nextgeneration sequencing reads

FastProNGS: Fast preprocessing of nextgeneration sequencing reads
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FastqCleaner: An interactive Bioconductor application for quality-control, filtering and trimming of FASTQ files

FastqCleaner: An interactive Bioconductor application for quality-control, filtering and trimming of FASTQ files
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Comparing the performance of selected variant callers using synthetic data and genome segmentation

Comparing the performance of selected variant callers using synthetic data and genome segmentation
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BrownieAligner: Accurate alignment of Illumina sequencing data to de Bruijn graphs

BrownieAligner: Accurate alignment of Illumina sequencing data to de Bruijn graphs
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DeviCNV: Detection and visualization of exon-level copy number variants in targeted next-generation sequencing data

DeviCNV: Detection and visualization of exon-level copy number variants in targeted next-generation sequencing data
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A fully automated pipeline for quantitative genotype calling from next generation sequencing data in autopolyploids

A fully automated pipeline for quantitative genotype calling from next generation sequencing data in autopolyploids
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Norgal: Extraction and de novo assembly of mitochondrial DNA from whole-genome sequencing data

Norgal: Extraction and de novo assembly of mitochondrial DNA from whole-genome sequencing data
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