"Genetic variants" trang 1 - tải miễn phí từ tailieuXANH
FAVR (Filtering and Annotation of Variants that are Rare): Methods to facilitate the analysis of rare germline genetic variants from massively parallel sequencing datasets

FAVR (Filtering and Annotation of Variants that are Rare): Methods to facilitate the analysis of rare germline genetic variants from massively parallel sequencing datasets
9    181    0
Three-dimensional spatial analysis of missense variants in RTEL1 identifies pathogenic variants in patients with Familial Interstitial Pneumonia

Three-dimensional spatial analysis of missense variants in RTEL1 identifies pathogenic variants in patients with Familial Interstitial Pneumonia
10    50    0
The association of megalin and cubilin genetic variants with serum levels of 25-hydroxvitamin D and the incidence of acute coronary syndrome in Egyptians: A case control study

The association of megalin and cubilin genetic variants with serum levels of 25-hydroxvitamin D and the incidence of acute coronary syndrome in Egyptians: A case control study
8    58    0
HMMvar-func: A new method for predicting the functional outcome of genetic variants

HMMvar-func: A new method for predicting the functional outcome of genetic variants
10    44    0
Genome-wide characterization of genetic variants and putative regions under selection in meat and egg-type chicken lines

Genome-wide characterization of genetic variants and putative regions under selection in meat and egg-type chicken lines
18    150    1
High-performance web services for querying gene and variant annotation

High-performance web services for querying gene and variant annotation
7    183    1
Accumulation of genetic variants associated with immunity in the selective breeding of broilers

Accumulation of genetic variants associated with immunity in the selective breeding of broilers
14    7    1
Spectrum of Germline RET variants identified by targeted sequencing and associated Multiple Endocrine Neoplasia type 2 susceptibility in China

Spectrum of Germline RET variants identified by targeted sequencing and associated Multiple Endocrine Neoplasia type 2 susceptibility in China
17    35    1
Genetic architecture of quantitative traits in beef cattle revealed by genome wide association studies of imputed whole genome sequence variants: II: Carcass merit traits

Genetic architecture of quantitative traits in beef cattle revealed by genome wide association studies of imputed whole genome sequence variants: II: Carcass merit traits
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Genetic architecture of quantitative traits in beef cattle revealed by genome wide association studies of imputed whole genome sequence variants: I: Feed efficiency and component traits

Genetic architecture of quantitative traits in beef cattle revealed by genome wide association studies of imputed whole genome sequence variants: I: Feed efficiency and component traits
22    80    1
Genetic variants in nuclear DNA along with environmental factors modify mitochondrial DNA copy number: A population-based exome-wide association study

Genetic variants in nuclear DNA along with environmental factors modify mitochondrial DNA copy number: A population-based exome-wide association study
9    67    1
Genetic variants in AKR1B10 associate with human eating behavior

Genetic variants in AKR1B10 associate with human eating behavior
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FUT2 genetic variants as predictors of tumor development with hepatocellular carcinoma

FUT2 genetic variants as predictors of tumor development with hepatocellular carcinoma
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Association of CARD10 rs6000782 and TNF rs1799724 variants with paediatric-onset autoimmune hepatitis

Association of CARD10 rs6000782 and TNF rs1799724 variants with paediatric-onset autoimmune hepatitis
8    46    0
Citrus tristeza virus variants and their distribution in mandarin orchards in northeastern Himalayan Hill region of India

Citrus tristeza virus variants and their distribution in mandarin orchards in northeastern Himalayan Hill region of India
11    49    0
Integrating 400 million variants from 80,000 human samples with extensive annotations: Towards a knowledge base to analyze disease cohorts

Integrating 400 million variants from 80,000 human samples with extensive annotations: Towards a knowledge base to analyze disease cohorts
13    63    0
The effect of rare variants on inflation of the test statistics in case–control analyses

The effect of rare variants on inflation of the test statistics in case–control analyses
5    54    0
Association of cervical carcinogenesis risk with HPV16 E6 and E7 variants in the Taizhou area, China

Association of cervical carcinogenesis risk with HPV16 E6 and E7 variants in the Taizhou area, China
9    76    1
Characterisation of genetic regulatory effects for osteoporosis risk variants in human osteoclasts

Characterisation of genetic regulatory effects for osteoporosis risk variants in human osteoclasts
13    150    1
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
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