variant analysis trang 2 tải miễn phí từ TAILIEUCHUNG

"variant analysis" trang 2 - tải miễn phí từ Tailieuchung

Ideal Profile Method: A comparison between rating and ranking technique

7 74 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 79 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 29 1

DNAscan: Personal computer compatible NGS analysis, annotation and visualisation

DNAscan: Personal computer compatible NGS analysis, annotation and visualisation

10 49 1

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 36 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 20 1

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 43 1

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 25 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 23 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 9 2

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 35 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 29 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 41 1

TSVdb: A web-tool for TCGA splicing variants analysis

TSVdb: A web-tool for TCGA splicing variants analysis

7 39 1

Improving somatic variant identification through integration of genome and exome data

Improving somatic variant identification through integration of genome and exome data

9 17 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 36 3

Gramtools enables multiscale variation analysis with genome graphs

Gramtools enables multiscale variation analysis with genome graphs

27 36 1

Vcfanno: Fast, flexible annotation of genetic variants

Vcfanno: Fast, flexible annotation of genetic variants

9 43 2

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 13 1

Can upfront DPYD extended variant testing reduce toxicity and associated hospital costs of fuoropyrimidine chemotherapy? A propensity score matched analysis of 2022 UK patients

Can upfront DPYD extended variant testing reduce toxicity and associated hospital costs of fuoropyrimidine chemotherapy? A propensity score matched analysis of 2022 UK patients

11 7 1

Đã phát hiện trình chặn quảng cáo AdBlock

Trang web này phụ thuộc vào doanh thu từ số lần hiển thị quảng cáo để tồn tại. Vui lòng tắt trình chặn quảng cáo của bạn hoặc tạm dừng tính năng chặn quảng cáo cho trang web này.