"Exome sequencing" trang 1 - tải miễn phí từ tailieunhanh
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    90    0
Opportunities and challenges of whole-genome and exome sequencing

Opportunities and challenges of whole-genome and exome sequencing
13    24    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    64    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    34    1
A new massively parallel nanoball sequencing platform for whole exome research

A new massively parallel nanoball sequencing platform for whole exome research
9    63    1
Variant detection sensitivity and biases in whole genome and exome sequencing

Variant detection sensitivity and biases in whole genome and exome sequencing
11    52    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
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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    67    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    52    1
Whole exome sequencing in the rat

Whole exome sequencing in the rat
14    43    1
Beyond the exome: Utility of long-read whole genome sequencing in exome-negative autosomal recessive diseases

Beyond the exome: Utility of long-read whole genome sequencing in exome-negative autosomal recessive diseases
16    11    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    30    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    70    1
Genomic alterations in gastric cancers discovered via whole-exome sequencing

Genomic alterations in gastric cancers discovered via whole-exome sequencing
12    65    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    53    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    50    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    62    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    50    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    85    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    99    1