"Single nucleotide variant" trang 1 - tải miễn phí từ tailieunhanh
QQ-SNV: Single nucleotide variant detection at low frequency by comparing the quality quantiles

QQ-SNV: Single nucleotide variant detection at low frequency by comparing the quality quantiles
14    40    1
Variant effect predictions capture some aspects of deep mutational scanning experiments

Variant effect predictions capture some aspects of deep mutational scanning experiments
12    41    1
Systematic comparative analysis of singlenucleotide variant detection methods from single-cell RNA sequencing data

Systematic comparative analysis of singlenucleotide variant detection methods from single-cell RNA sequencing data
15    67    3
Whole genome resequencing of the Iranian native dogs and wolves to unravel variome during dog domestication

Whole genome resequencing of the Iranian native dogs and wolves to unravel variome during dog domestication
11    20    2
The single nucleotide β -arrestin2 variant, A248T, resembles dynamical properties of activated arrestin

The single nucleotide β -arrestin2 variant, A248T, resembles dynamical properties of activated arrestin
12    20    1
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    18    1
A genetic variant of the NTCP gene is associated with HBV infection status in a Chinese population

A genetic variant of the NTCP gene is associated with HBV infection status in a Chinese population
8    66    1
Loqusdb: Added value of an observations database of local genomic variation

Loqusdb: Added value of an observations database of local genomic variation
10    54    1
TNER: A novel background error suppression method for mutation detection in circulating tumor DNA

TNER: A novel background error suppression method for mutation detection in circulating tumor DNA
7    65    1
PRINCESS: Comprehensive detection of haplotype resolved SNVs, SVs, and methylation

PRINCESS: Comprehensive detection of haplotype resolved SNVs, SVs, and methylation
17    44    1
Variant site strain typer (VaST): Efficient strain typing using a minimal number of variant genomic sites

Variant site strain typer (VaST): Efficient strain typing using a minimal number of variant genomic sites
13    43    1
A functional genetic variant in fragile-site gene FATS modulates the risk of breast cancer in triparous women

A functional genetic variant in fragile-site gene FATS modulates the risk of breast cancer in triparous women
11    29    1
A pri-miR-218 variant and risk of cervical carcinoma in Chinese women

A pri-miR-218 variant and risk of cervical carcinoma in Chinese women
8    68    1
SV-Pop: Population-based structural variant analysis and visualization

SV-Pop: Population-based structural variant analysis and visualization
4    58    1
Germline contamination and leakage in whole genome somatic single nucleotide variant detection

Germline contamination and leakage in whole genome somatic single nucleotide variant detection
9    57    1
An integrative approach to predicting the functional effects of small indels in non-coding regions of the human genome

An integrative approach to predicting the functional effects of small indels in non-coding regions of the human genome
8    63    1
Performance of copy number variants detection based on whole‑genome sequencing by DNBSEQ platforms

Performance of copy number variants detection based on whole‑genome sequencing by DNBSEQ platforms
14    31    1
Snp-search: Simple processing, manipulation and searching of SNPs from high-throughput sequencing

Snp-search: Simple processing, manipulation and searching of SNPs from high-throughput sequencing
8    36    1
A case–control study of innate immunity pathway gene polymorphisms in Puerto Ricans reveals association of toll-like receptor 2 +596 variant with asthma

A case–control study of innate immunity pathway gene polymorphisms in Puerto Ricans reveals association of toll-like receptor 2 +596 variant with asthma
11    34    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