"allele cyp2c192" trang 7 - tải miễn phí từ tailieuXANH
Investigation of ancestral alleles in the Bovinae subfamily

Investigation of ancestral alleles in the Bovinae subfamily
12    47    1
Investigating the accuracy of imputing autosomal variants in Nellore cattle using the ARS-UCD1.2 assembly of the bovine genome

Investigating the accuracy of imputing autosomal variants in Nellore cattle using the ARS-UCD1.2 assembly of the bovine genome
12    73    1
Deep sampling and pooled amplicon sequencing reveals hidden genic variation in heterogeneous rye accessions

Deep sampling and pooled amplicon sequencing reveals hidden genic variation in heterogeneous rye accessions
16    24    1
How to study runs of homozygosity using PLINK? A guide for analyzing medium density SNP data in livestock and pet species

How to study runs of homozygosity using PLINK? A guide for analyzing medium density SNP data in livestock and pet species
14    47    1
Evolution of cis- and trans-regulatory divergence in the chicken genome between two contrasting breeds analyzed using three tissue types at one-day-old

Evolution of cis- and trans-regulatory divergence in the chicken genome between two contrasting breeds analyzed using three tissue types at one-day-old
10    238    2
Nghiên cứu phân bố kiểu gene CYP1A1 tại vị trí đa hình (rs4646903) trên đối tượng phơi nhiễm dioxin

Nghiên cứu phân bố kiểu gene CYP1A1 tại vị trí đa hình (rs4646903) trên đối tượng phơi nhiễm dioxin
5    54    2
Human genes escaping X-inactivation revealed by single cell expression data

Human genes escaping X-inactivation revealed by single cell expression data
17    36    1
SCReadCounts: Estimation of cell-level SNVs expression from scRNA-seq data

SCReadCounts: Estimation of cell-level SNVs expression from scRNA-seq data
9    245    1
Systematic evaluation of signal-to-noise ratio in variant detection from single cell genome multiple displacement amplification and exome sequencing

Systematic evaluation of signal-to-noise ratio in variant detection from single cell genome multiple displacement amplification and exome sequencing
9    152    1
Combining QTL-seq and linkage mapping to fine map a wild soybean allele characteristic of greater plant height

Combining QTL-seq and linkage mapping to fine map a wild soybean allele characteristic of greater plant height
12    243    1
Genome-wide identification of Chiari malformation type I associated candidate genes and chromosomal variations

Genome-wide identification of Chiari malformation type I associated candidate genes and chromosomal variations
13    249    1
The Tug1 lncRNA locus is essential for male fertility

The Tug1 lncRNA locus is essential for male fertility
35    25    1
Regulatory regions in natural transposable element insertions drive interindividual differences in response to immune challenges in Drosophila

Regulatory regions in natural transposable element insertions drive interindividual differences in response to immune challenges in Drosophila
30    155    1
Bovine breed-specific augmented reference graphs facilitate accurate sequence read mapping and unbiased variant discovery

Bovine breed-specific augmented reference graphs facilitate accurate sequence read mapping and unbiased variant discovery
27    188    1
Kourami: Graph-guided assembly for novel human leukocyte antigen allele discovery

Kourami: Graph-guided assembly for novel human leukocyte antigen allele discovery
16    50    2
GAVIN: Gene-Aware Variant INterpretation for medical sequencing

GAVIN: Gene-Aware Variant INterpretation for medical sequencing
10    218    2
EpiG: Statistical inference and profiling of DNA methylation from whole-genome bisulfite sequencing data

EpiG: Statistical inference and profiling of DNA methylation from whole-genome bisulfite sequencing data
16    26    2
AlleleAnalyzer: A tool for personalized and allele-specific sgRNA design

AlleleAnalyzer: A tool for personalized and allele-specific sgRNA design
9    132    2
Genotype-free demultiplexing of pooled single-cell RNA-seq

Genotype-free demultiplexing of pooled single-cell RNA-seq
12    37    2
CTCF modulates allele-specific sub-TAD organization and imprinted gene activity at the mouse Dlk1-Dio3 and Igf2-H19 domains

CTCF modulates allele-specific sub-TAD organization and imprinted gene activity at the mouse Dlk1-Dio3 and Igf2-H19 domains
17    119    2
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