"variant analysis" trang 2 - tải miễn phí từ tailieuXANH
Báo cáo khoa học: Regulation of ascidian Rel by its alternative splice variant

Báo cáo khoa học: Regulation of ascidian Rel by its alternative splice variant
10    58    0
Ideal Profile Method: A comparison between rating and ranking technique

Ideal Profile Method: A comparison between rating and ranking technique
7    129    0
Technical advance in targeted NGS analysis enables identification of lung cancer riskassociated low frequency TP53, PIK3CA, and BRAF mutations in airway epithelial cells

Technical advance in targeted NGS analysis enables identification of lung cancer riskassociated low frequency TP53, PIK3CA, and BRAF mutations in airway epithelial cells
14    69    0
A genetic variant in long non-coding RNA MALAT1 associated with survival outcome among patients with advanced lung adenocarcinoma: A survival cohort analysis

A genetic variant in long non-coding RNA MALAT1 associated with survival outcome among patients with advanced lung adenocarcinoma: A survival cohort analysis
8    65    0
DNAscan: Personal computer compatible NGS analysis, annotation and visualisation

DNAscan: Personal computer compatible NGS analysis, annotation and visualisation
10    53    0
A comparison of genotyping-by-sequencing analysis methods on low-coverage crop datasets shows advantages of a new workflow, GB-eaSy

A comparison of genotyping-by-sequencing analysis methods on low-coverage crop datasets shows advantages of a new workflow, GB-eaSy
12    56    0
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    124    0
Launching genomics into the cloud: Deployment of Mercury, a next generation sequence analysis pipeline

Launching genomics into the cloud: Deployment of Mercury, a next generation sequence analysis pipeline
11    86    0
Comprehensive analysis of germline mutations in northern Brazil: A panel of 16 genes for hereditary cancer-predisposing syndrome investigation

Comprehensive analysis of germline mutations in northern Brazil: A panel of 16 genes for hereditary cancer-predisposing syndrome investigation
8    37    1
Challenging the diagnosis of Cystic Fibrosis in a patient carrying the 186-8T/C allelic variant in the CF Transmembrane Conductance Regulator gene

Challenging the diagnosis of Cystic Fibrosis in a patient carrying the 186-8T/C allelic variant in the CF Transmembrane Conductance Regulator gene
7    36    1
Genome-wide association analysis of canine T zone lymphoma identifies link to hypothyroidism and a shared association with mast-cell tumors

Genome-wide association analysis of canine T zone lymphoma identifies link to hypothyroidism and a shared association with mast-cell tumors
11    272    1
A clinically validated whole genome pipeline for structural variant detection and analysis

A clinically validated whole genome pipeline for structural variant detection and analysis
8    56    1
Comparative analysis of the chicken IFITM locus by targeted genome sequencing reveals evolution of the locus and positive selection in IFITM1 and IFITM3

Comparative analysis of the chicken IFITM locus by targeted genome sequencing reveals evolution of the locus and positive selection in IFITM1 and IFITM3
14    37    1
Genome-wide copy number variant analysis reveals variants associated with 10 diverse production traits in Holstein cattle

Genome-wide copy number variant analysis reveals variants associated with 10 diverse production traits in Holstein cattle
9    176    1
TSVdb: A web-tool for TCGA splicing variants analysis

TSVdb: A web-tool for TCGA splicing variants analysis
7    244    1
Improving somatic variant identification through integration of genome and exome data

Improving somatic variant identification through integration of genome and exome data
9    142    1
Identification of an at-risk subpopulation with high immune infiltration based on the peroxisome pathway and TIM3 in colorectal cancer

Identification of an at-risk subpopulation with high immune infiltration based on the peroxisome pathway and TIM3 in colorectal cancer
17    188    2
Gramtools enables multiscale variation analysis with genome graphs

Gramtools enables multiscale variation analysis with genome graphs
27    95    1
Vcfanno: Fast, flexible annotation of genetic variants

Vcfanno: Fast, flexible annotation of genetic variants
9    137    1
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
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