Exome sequencing trang 1 tải miễn phí từ TAILIEUCHUNG

"Exome sequencing" trang 1 - tải miễn phí từ Tailieuchung

Whole exome sequencing pipeline evaluation and mutation detection in esophageal cancer patients

Whole exome sequencing pipeline evaluation and mutation detection in esophageal cancer patients

9 69 0

Performance assessment of variant calling pipelines using human whole exome sequencing and simulated data

Performance assessment of variant calling pipelines using human whole exome sequencing and simulated data

11 46 1

Identification of a de novo mutation in KRT5 gene underlying epidermolysis bullosa simplex by whole exome sequencing in a Vietnamese patient

Identification of a de novo mutation in KRT5 gene underlying epidermolysis bullosa simplex by whole exome sequencing in a Vietnamese patient

6 22 1

A new massively parallel nanoball sequencing platform for whole exome research

A new massively parallel nanoball sequencing platform for whole exome research

9 44 1

Variant detection sensitivity and biases in whole genome and exome sequencing

Variant detection sensitivity and biases in whole genome and exome sequencing

11 31 1

Shared genetic susceptibilities for irritable bowel syndrome and depressive disorder in Chinese patients uncovered by pooled whole-exome sequencing

Shared genetic susceptibilities for irritable bowel syndrome and depressive disorder in Chinese patients uncovered by pooled whole-exome sequencing

9 81 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 48 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 39 1

Whole exome sequencing in the rat

Whole exome sequencing in the rat

14 23 1

Systematic evaluation of signal-to-noise ratio in variant detection from single cell genome multiple displacement amplification and exome sequencing

Systematic evaluation of signal-to-noise ratio in variant detection from single cell genome multiple displacement amplification and exome sequencing

9 14 1

Whole exome sequencing of an asbestosinduced wild-type murine model of malignant mesothelioma

Whole exome sequencing of an asbestosinduced wild-type murine model of malignant mesothelioma

10 56 1

Genomic alterations in gastric cancers discovered via whole-exome sequencing

Genomic alterations in gastric cancers discovered via whole-exome sequencing

12 50 1

Case report: Whole exome sequencing of primary cardiac angiosarcoma highlights potential for targeted therapies

Case report: Whole exome sequencing of primary cardiac angiosarcoma highlights potential for targeted therapies

10 39 1

Identification of somatic and germline mutations using whole exome sequencing of congenital acute lymphoblastic leukemia

Identification of somatic and germline mutations using whole exome sequencing of congenital acute lymphoblastic leukemia

6 34 1

Anaconda: AN automated pipeline for somatic COpy Number variation Detection and Annotation from tumor exome sequencing data

Anaconda: AN automated pipeline for somatic COpy Number variation Detection and Annotation from tumor exome sequencing data

6 47 1

An evaluation of copy number variation detection tools for cancer using whole exome sequencing data

An evaluation of copy number variation detection tools for cancer using whole exome sequencing data

13 31 1

Detailed simulation of cancer exome sequencing data reveals differences and common limitations of variant callers

Detailed simulation of cancer exome sequencing data reveals differences and common limitations of variant callers

15 69 1

CloneCNA: Detecting subclonal somatic copy number alterations in heterogeneous tumor samples from whole-exome sequencing data

CloneCNA: Detecting subclonal somatic copy number alterations in heterogeneous tumor samples from whole-exome sequencing data

10 81 1

VEGAWES: Variational segmentation on whole exome sequencing for copy number detection

VEGAWES: Variational segmentation on whole exome sequencing for copy number detection

10 37 1

Association of a rare NOTCH4 coding variant with systemic sclerosis: A family-based whole exome sequencing study

Association of a rare NOTCH4 coding variant with systemic sclerosis: A family-based whole exome sequencing study

6 27 1

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