Rare genetic variants trang 1 tải miễn phí từ tailieuXANH

"Rare 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

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

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

NCBoost classifies pathogenic non-coding variants in Mendelian diseases through supervised learning on purifying selection signals in humans

NCBoost classifies pathogenic non-coding variants in Mendelian diseases through supervised learning on purifying selection signals in humans

22 16 1

The effect of rare alleles on estimated genomic relationships from whole genome sequence data

The effect of rare alleles on estimated genomic relationships from whole genome sequence data

12 2 1

The impact of rare and low-frequency genetic variants in common disease

The impact of rare and low-frequency genetic variants in common disease

17 206 2

A rare case of pediatric recurrent rhabdomyolysis with compound heterogenous variants in the LPIN1

A rare case of pediatric recurrent rhabdomyolysis with compound heterogenous variants in the LPIN1

6 49 0

A burden of rare variants in BMPR2 and KCNK3 contributes to a risk of familial pulmonary arterial hypertension

A burden of rare variants in BMPR2 and KCNK3 contributes to a risk of familial pulmonary arterial hypertension

8 41 1

Rare intronic variants of TCF7L2 arising by selective sweeps in an indigenous population from Mexico

Rare intronic variants of TCF7L2 arising by selective sweeps in an indigenous population from Mexico

15 2 1

A method to incorporate prior information into score test for genetic association studies

A method to incorporate prior information into score test for genetic association studies

10 56 0

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