"mutation estimators" trang 9 - tải miễn phí từ tailieuXANH
Achieving robust somatic mutation detection with deep learning models derived from reference data sets of a cancer sample

Achieving robust somatic mutation detection with deep learning models derived from reference data sets of a cancer sample
20    200    1
MuSE: Accounting for tumor heterogeneity using a sample-specific error model improves sensitivity and specificity in mutation calling from sequencing data

MuSE: Accounting for tumor heterogeneity using a sample-specific error model improves sensitivity and specificity in mutation calling from sequencing data
11    171    1
The somatic mutation landscape of the human body

The somatic mutation landscape of the human body
20    161    2
Reduced intrinsic DNA curvature leads to increased mutation rate

Reduced intrinsic DNA curvature leads to increased mutation rate
12    16    1
Prognostic impact of pretreatment T790M mutation on outcomes for patients with resected, EGFR-mutated, non-small cell lung cancer

Prognostic impact of pretreatment T790M mutation on outcomes for patients with resected, EGFR-mutated, non-small cell lung cancer
11    20    1
Clinical application of liquid biopsy in cancer patients

Clinical application of liquid biopsy in cancer patients
9    18    1
Detection of EGFR mutation and its association with clinicopathological features of non-small cell lung cancer patients

Detection of EGFR mutation and its association with clinicopathological features of non-small cell lung cancer patients
5    8    1
The mtDNA mutation spectrum in the PolG mutator mouse reveals germline and somatic selection

The mtDNA mutation spectrum in the PolG mutator mouse reveals germline and somatic selection
15    10    1
Functional mutation allele mining of plant architecture and yield-related agronomic traits and characterization of their effects in wheat

Functional mutation allele mining of plant architecture and yield-related agronomic traits and characterization of their effects in wheat
15    7    1
Phenotypic Heterogeneity in a DFNA20/26 family segregating a novel ACTG1 mutation

Phenotypic Heterogeneity in a DFNA20/26 family segregating a novel ACTG1 mutation
11    2    1
The high frequency of GJB2 gene mutation c.313_326del14 suggests its possible origin in ancestors of Lithuanian population

The high frequency of GJB2 gene mutation c.313_326del14 suggests its possible origin in ancestors of Lithuanian population
12    2    1
A nonsense mutation in the COL7A1 gene causes epidermolysis bullosa in Vorderwald cattle

A nonsense mutation in the COL7A1 gene causes epidermolysis bullosa in Vorderwald cattle
9    2    1
Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation

Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation
8    3    1
Investigation of a recent rise of dual amantadineresistance mutations in the influenza A M2 sequence

Investigation of a recent rise of dual amantadineresistance mutations in the influenza A M2 sequence
9    2    1
Novel technique for rapid detection of a-globin gene mutations and deletions

Novel technique for rapid detection of a-globin gene mutations and deletions
8    36    0
Mutation analysis of EGFR and FGFR gene in glioblastoma patients in Vietnam

Mutation analysis of EGFR and FGFR gene in glioblastoma patients in Vietnam
6    100    0
TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus

TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus
10    45    0
Revalence and spectrum of TBX5 mutation in patients with lone atrial fibrillation

Revalence and spectrum of TBX5 mutation in patients with lone atrial fibrillation
8    46    0
Mutation breeding in pulses to curb malnutrition

Mutation breeding in pulses to curb malnutrition
29    49    0
Genetic investigation confirmed the clinical phenotype of congenital chloride diarrhea in a Hungarian patient: A case report

Genetic investigation confirmed the clinical phenotype of congenital chloride diarrhea in a Hungarian patient: A case report
4    85    0
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