"dna single strand breaks" trang 4 - tải miễn phí từ tailieunhanh
Báo cáo khoa học: Kinetic study of the HIV)1 DNA 3¢-end processing Single-turnover property of integrase

Báo cáo khoa học: Kinetic study of the HIV)1 DNA 3¢-end processing Single-turnover property of integrase
15    29    0
Báo cáo khoa học: Formation of nucleoprotein RecA filament on single-stranded DNA Analysis by stepwise increase in ligand complexity

Báo cáo khoa học: Formation of nucleoprotein RecA filament on single-stranded DNA Analysis by stepwise increase in ligand complexity
1    47    0
Báo cáo khoa học: Interaction of the C1 complex of Complement with sulfated polysaccharide and DNA probed by single molecule fluorescence microscopy

Báo cáo khoa học: Interaction of the C1 complex of Complement with sulfated polysaccharide and DNA probed by single molecule fluorescence microscopy
7    103    0
Genetic variability in drug transport, metabolism or DNA repair affecting toxicity of chemotherapy in ovarian cancer

Genetic variability in drug transport, metabolism or DNA repair affecting toxicity of chemotherapy in ovarian cancer
13    78    0
ddRAD sequencing-based identification of inter-genepool SNPs and association analysis in Brassica juncea

ddRAD sequencing-based identification of inter-genepool SNPs and association analysis in Brassica juncea
15    80    0
A single blastocyst assay optimized for detecting CRISPR/Cas9 system-induced indel mutations in mice

A single blastocyst assay optimized for detecting CRISPR/Cas9 system-induced indel mutations in mice
11    86    0
NBS1 rs2735383 polymorphism is associated with an increased risk of laryngeal carcinoma

NBS1 rs2735383 polymorphism is associated with an increased risk of laryngeal carcinoma
8    58    1
Association between polymorphisms in ERCC2 gene and oral cancer risk: Evidence from a meta-analysis

Association between polymorphisms in ERCC2 gene and oral cancer risk: Evidence from a meta-analysis
8    43    1
Clinical variables serve as prognostic factors in a model for survival from glioblastoma multiforme: An observational study of a cohort of consecutive non-selected patients from a single institution

Clinical variables serve as prognostic factors in a model for survival from glioblastoma multiforme: An observational study of a cohort of consecutive non-selected patients from a single institution
11    41    1
Protein–protein and protein‑nucleic acid binding residues important for common and rare sequence variants in human

Protein–protein and protein‑nucleic acid binding residues important for common and rare sequence variants in human
17    56    1
Sensitive detection of circular DNAs at single-nucleotide resolution using guided realignment of partially aligned reads

Sensitive detection of circular DNAs at single-nucleotide resolution using guided realignment of partially aligned reads
9    78    1
Valection: Design optimization for validation and verification studies

Valection: Design optimization for validation and verification studies
11    75    1
TNER: A novel background error suppression method for mutation detection in circulating tumor DNA

TNER: A novel background error suppression method for mutation detection in circulating tumor DNA
7    65    1
TIA: Algorithms for development of identity-linked SNP islands for analysis by massively parallel DNA sequencing

TIA: Algorithms for development of identity-linked SNP islands for analysis by massively parallel DNA sequencing
13    58    1
BS-Seeker3: Ultrafast pipeline for bisulfite sequencing

BS-Seeker3: Ultrafast pipeline for bisulfite sequencing
4    47    1
DMRfinder: Efficiently identifying differentially methylated regions from MethylC-seq data

DMRfinder: Efficiently identifying differentially methylated regions from MethylC-seq data
8    72    1
FoCo: A simple and robust quantification algorithm of nuclear foci

FoCo: A simple and robust quantification algorithm of nuclear foci
13    41    1
Afull Bayesian partitionmodelfor identifying hypo- and hyper-methylated loci from single nucleotide resolution sequencing data

Afull Bayesian partitionmodelfor identifying hypo- and hyper-methylated loci from single nucleotide resolution sequencing data
13    43    1
DRUMS: Disk Repository with Update Management and Select option for high throughput sequencing data

DRUMS: Disk Repository with Update Management and Select option for high throughput sequencing data
9    67    1
SubPatCNV: Approximate subspace pattern mining for mapping copy-number variations

SubPatCNV: Approximate subspace pattern mining for mapping copy-number variations
12    46    1