"Sequence variants" trang 1 - tải miễn phí từ tailieunhanh
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
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
22    37    2
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    38    2
Prevalence of BRCA1 and BRCA2 pathogenic sequence variants in ovarian cancer patients in the Gulf region: The PREDICT study

Prevalence of BRCA1 and BRCA2 pathogenic sequence variants in ovarian cancer patients in the Gulf region: The PREDICT study
8    27    3
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    65    1
Rare variants analysis using penalization methods for whole genome sequence data

Rare variants analysis using penalization methods for whole genome sequence data
8    80    1
Detection of copy number variants in African goats using whole genome sequence data

Detection of copy number variants in African goats using whole genome sequence data
15    48    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
Whole genome sequence analysis of serum amino acid levels

Whole genome sequence analysis of serum amino acid levels
10    28    3
Genome-wide association analysis of milk yield traits in Nordic Red Cattle using imputed whole genome sequence variants

Genome-wide association analysis of milk yield traits in Nordic Red Cattle using imputed whole genome sequence variants
12    6    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    14    1
Fast imputation using medium or low-coverage sequence data

Fast imputation using medium or low-coverage sequence data
12    19    1
Báo cáo y học:

Báo cáo y học: "Targeted next-generation sequencing of a cancer transcriptome enhances detection of sequence variants and novel fusion transcript"
1    44    0
Báo cáo y học:

Báo cáo y học: "HLA-G DNA sequence variants and risk of perinatal HIV-1 transmission"
8    45    0
Báo cáo khoa học: Sequence variants of chicken linker histone H1.a

Báo cáo khoa học: Sequence variants of chicken linker histone H1.a
11    59    0
Family reunion via error correction: An efficient analysis of duplex sequencing data

Family reunion via error correction: An efficient analysis of duplex sequencing data
10    36    1
MC-GenomeKey: A multicloud system for the detection and annotation of genomic variants

MC-GenomeKey: A multicloud system for the detection and annotation of genomic variants
14    77    1
An heuristic filtering tool to identify phenotype-associated genetic variants applied to human intellectual disability and canine coat colors

An heuristic filtering tool to identify phenotype-associated genetic variants applied to human intellectual disability and canine coat colors
7    30    1
Natrix: A Snakemake‑based workfow for processing, clustering, and taxonomically assigning amplicon sequencing reads

Natrix: A Snakemake‑based workfow for processing, clustering, and taxonomically assigning amplicon sequencing reads
14    42    1
Population genetic analysis of bi-allelic structural variants from low-coverage sequence data with an expectation-maximization algorithm

Population genetic analysis of bi-allelic structural variants from low-coverage sequence data with an expectation-maximization algorithm
13    49    1