Whole exome sequencing trang 1 tải miễn phí từ TAILIEUCHUNG

"Whole 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

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

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

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

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

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

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

Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data

Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data

18 31 1

An ancestry informative marker panel design for individual ancestry estimation of Hispanic population using whole exome sequencing data

An ancestry informative marker panel design for individual ancestry estimation of Hispanic population using whole exome sequencing data

14 35 2

NAPG mutation in family members with hereditary hemorrhagic telangiectasia in China

NAPG mutation in family members with hereditary hemorrhagic telangiectasia in China

9 29 1

Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing

Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing

26 18 3

ALPHLARD: A Bayesian method for analyzing HLA genes from whole genome sequence data

ALPHLARD: A Bayesian method for analyzing HLA genes from whole genome sequence data

11 24 1

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