"Human genomics data" trang 1 - tải miễn phí từ tailieunhanh
MethCNA: A database for integrating genomic and epigenomic data in human cancer

MethCNA: A database for integrating genomic and epigenomic data in human cancer
10    46    1
A standardized framework for representation of ancestry data in genomics studies, with application to the NHGRI-EBI GWAS Catalog

A standardized framework for representation of ancestry data in genomics studies, with application to the NHGRI-EBI GWAS Catalog
10    29    3
Origins and characterization of variants shared between databases of somatic and germline human mutations

Origins and characterization of variants shared between databases of somatic and germline human mutations
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Evaluating the quality of the 1000 genomes project data

Evaluating the quality of the 1000 genomes project data
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Genome-wide prediction and prioritization of human aging genes by data fusion: A machine learning approach

Genome-wide prediction and prioritization of human aging genes by data fusion: A machine learning approach
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Big data analysis of human mitochondrial DNA substitution models: A regression approach

Big data analysis of human mitochondrial DNA substitution models: A regression approach
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Characteristics of allelic gene expression in human brain cells from single-cell RNA-seq data analysis

Characteristics of allelic gene expression in human brain cells from single-cell RNA-seq data analysis
18    34    1
A vast resource of allelic expression data spanning human tissues

A vast resource of allelic expression data spanning human tissues
12    31    1
Weighted likelihood inference of genomic autozygosity patterns in dense genotype data

Weighted likelihood inference of genomic autozygosity patterns in dense genotype data
33    28    1
Integrative analysis and machine learning on cancer genomics data using the Cancer Systems Biology Database (CancerSysDB)

Integrative analysis and machine learning on cancer genomics data using the Cancer Systems Biology Database (CancerSysDB)
10    78    1
Evaluation of tools for identifying large copy number variations from ultra-lowcoverage whole-genome sequencing data

Evaluation of tools for identifying large copy number variations from ultra-lowcoverage whole-genome sequencing data
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Rapid single cell evaluation of human disease and disorder targets using REVEAL: SingleCell

Rapid single cell evaluation of human disease and disorder targets using REVEAL: SingleCell
12    44    1
Blood-based epigenetic estimators of chronological age in human adults using DNA methylation data from the Illumina MethylationEPIC array

Blood-based epigenetic estimators of chronological age in human adults using DNA methylation data from the Illumina MethylationEPIC array
13    40    1
Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data

Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
18    44    1
Sequencing of five poultry strains elucidates phylogenetic relationships and divergence in virulence genes in Morganella morganii

Sequencing of five poultry strains elucidates phylogenetic relationships and divergence in virulence genes in Morganella morganii
13    35    1
Population history and genetic adaptation of the Fulani nomads: Inferences from genome-wide data and the lactase persistence trait

Population history and genetic adaptation of the Fulani nomads: Inferences from genome-wide data and the lactase persistence trait
12    22    1
Recurrent miscalling of missense variation from short-read genome sequence data

Recurrent miscalling of missense variation from short-read genome sequence data
9    42    1
HumanMycobiomeScan: A new bioinformatics tool for the characterization of the fungal fraction in metagenomic samples

HumanMycobiomeScan: A new bioinformatics tool for the characterization of the fungal fraction in metagenomic samples
7    32    1
Challenges imposed by minor reference alleles on the identification and reporting of clinical variants from exome data

Challenges imposed by minor reference alleles on the identification and reporting of clinical variants from exome data
8    31    1
A maximum likelihood algorithm for reconstructing 3D structures of human chromosomes from chromosomal contact data

A maximum likelihood algorithm for reconstructing 3D structures of human chromosomes from chromosomal contact data
17    62    1