"Single nucleotide variants" trang 1 - tải miễn phí từ tailieuXANH
Concordance rate between copy number variants detected using either high- or medium-density single nucleotide polymorphism genotype panels and the potential of imputing copy number variants from flanking high density single nucleotide polymorphism haplotypes in cattle

Concordance rate between copy number variants detected using either high- or medium-density single nucleotide polymorphism genotype panels and the potential of imputing copy number variants from flanking high density single nucleotide polymorphism haplotypes in cattle
10    102    2
Accuracy of analysis of cfDNA for detection of single nucleotide variants and copy number variants in breast cancer

Accuracy of analysis of cfDNA for detection of single nucleotide variants and copy number variants in breast cancer
14    62    0
SNVHMM: Predicting single nucleotide variants from next generation sequencing

SNVHMM: Predicting single nucleotide variants from next generation sequencing
11    110    0
Genome-wide segregation of single nucleotide and structural variants into single cancer cells

Genome-wide segregation of single nucleotide and structural variants into single cancer cells
6    42    1
Optimized pipeline of MuTect and GATK tools to improve the detection of somatic single nucleotide polymorphisms in wholeexome sequencing data

Optimized pipeline of MuTect and GATK tools to improve the detection of somatic single nucleotide polymorphisms in wholeexome sequencing data
9    82    0
Inferring clonal evolution of tumors from single nucleotide somatic mutations

Inferring clonal evolution of tumors from single nucleotide somatic mutations
16    49    0
Genome-wide association analyses of carcass traits using copy number variants and raw intensity values of single nucleotide polymorphisms in cattle

Genome-wide association analyses of carcass traits using copy number variants and raw intensity values of single nucleotide polymorphisms in cattle
16    79    1
RegSNPs-intron: A computational framework for predicting pathogenic impact of intronic single nucleotide variants

RegSNPs-intron: A computational framework for predicting pathogenic impact of intronic single nucleotide variants
16    30    2
Identification of single-nucleotide variants associated with susceptibility to Salmonella in pigs using a genome-wide association approach

Identification of single-nucleotide variants associated with susceptibility to Salmonella in pigs using a genome-wide association approach
12    16    1
Representing and decomposing genomic structural variants as balanced integer flows on sequence graphs

Representing and decomposing genomic structural variants as balanced integer flows on sequence graphs
16    68    0
Identification of novel prostate cancer drivers using RegNetDriver: A framework for integration of genetic and epigenetic alterations with tissue-specific regulatory network

Identification of novel prostate cancer drivers using RegNetDriver: A framework for integration of genetic and epigenetic alterations with tissue-specific regulatory network
23    111    1
Assessing cell-specific effects of genetic variations using tRNA microarrays

Assessing cell-specific effects of genetic variations using tRNA microarrays
12    288    1
FUT2 genetic variants as predictors of tumor development with hepatocellular carcinoma

FUT2 genetic variants as predictors of tumor development with hepatocellular carcinoma
6    43    0
báo cáo khoa học:

báo cáo khoa học: " Ethical issues raised by common copy number variants and single nucleotide polymorphisms of certain and uncertain significance in general medical practice"
6    37    0
Association of genetic variants of small non-coding RNAs with survival in colorectal cancer

Association of genetic variants of small non-coding RNAs with survival in colorectal cancer
6    42    0
Genetic analysis of BDNF, GNB3, MTHFR, ACE and APOE variants in major and recurrent depressive disorders in Russia

Genetic analysis of BDNF, GNB3, MTHFR, ACE and APOE variants in major and recurrent depressive disorders in Russia
7    38    0
Natural variants of ELF3 affect thermomorphogenesis by transcriptionally modulating PIF4-dependent auxin response genes

Natural variants of ELF3 affect thermomorphogenesis by transcriptionally modulating PIF4-dependent auxin response genes
10    53    0
Association of DNA repair gene variants with colorectal cancer: Risk, toxicity, and survival

Association of DNA repair gene variants with colorectal cancer: Risk, toxicity, and survival
10    43    0
Effects of interactions between common genetic variants and smoking on colorectal cancer

Effects of interactions between common genetic variants and smoking on colorectal cancer
9    85    0
Psychosocial and behavioral impact of breast cancer risk assessed by testing for common risk variants: Protocol of a prospective study

Psychosocial and behavioral impact of breast cancer risk assessed by testing for common risk variants: Protocol of a prospective study
11    101    0
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